Suplements in Rehab

Download as pdf or txt
Download as pdf or txt
You are on page 1of 20

nutrients

Review
Nutritional Considerations for Injury Prevention and Recovery
in Combat Sports
Hüseyin Hüsrev Turnagöl *, Şükran Nazan Koşar , Yasemin Güzel , Selin Aktitiz
and Muhammed Mustafa Atakan
Division of Nutrition and Metabolism in Exercise, Faculty of Sport Sciences, Hacettepe University,
Ankara 06800, Turkey; [email protected] (Ş.N.K.); [email protected] (Y.G.);
[email protected] (S.A.); [email protected] (M.M.A.)
* Correspondence: [email protected]; Tel.: +90-312-297-68-90; Fax: +90-312-299-21-67

Abstract: Sports participation is not without risk, and most athletes incur at least one injury through-
out their careers. Combat sports are popular all around the world, and about one-third of their
injuries result in more than 7 days of absence from competition or training. The most frequently
injured body regions are the head and neck, followed by the upper and lower limbs, while the most
common tissue types injured are superficial tissues and skin, followed by ligaments and joint capsules.
Nutrition has significant implications for injury prevention and enhancement of the recovery process
due to its effect on the overall physical and psychological well-being of the athlete and improving
tissue healing. In particular, amino acid and protein intake, antioxidants, creatine, and omega-3 are
given special attention due to their therapeutic roles in preventing muscle loss and anabolic resistance
as well as promoting injury healing. The purpose of this review is to present the roles of various
nutritional strategies in reducing the risk of injury and improving the treatment and rehabilitation
process in combat sports. In this respect, nutritional considerations for muscle, joint, and bone injuries
as well as sports-related concussions are presented. The injury risk associated with rapid weight loss

 is also discussed. Finally, preoperative nutrition and nutritional considerations for returning to a
Citation: Turnagöl, H.H.; Koşar, Ş.N.; sport after rehabilitation are addressed.
Güzel, Y.; Aktitiz, S.; Atakan, M.M.
Nutritional Considerations for Injury Keywords: combat sports; nutrition; recovery from injury; sports injuries; supplements
Prevention and Recovery in Combat
Sports. Nutrients 2022, 14, 53.
https://doi.org/10.3390/nu14010053
1. Introduction
Academic Editors: Roberta Ceci and
Guglielmo Duranti Combat sports are characterized by repeated movements, including striking (kicking,
punching, and blocking defensive moves with the arms and legs), grappling, (wresting
Received: 30 October 2021
an opponent to the ground or using a submission hold), and combinations of these tech-
Accepted: 20 December 2021
niques [1]. Popular at competitive and recreational levels all over the world, combat
Published: 23 December 2021
sports improve physical fitness (e.g., increased muscle strength, flexibility, and balance),
Publisher’s Note: MDPI stays neutral psychological aspects (e.g., self-esteem, self-awareness, and self-respect), and cognitive
with regard to jurisdictional claims in function [1].
published maps and institutional affil- Sports participation is not without risk, and most athletes incur at least one injury
iations. throughout their careers. Olympic combat sport athletes sustain, on average, one injury
every 2.1 h of competition [2]. Furthermore, about 30% of the injuries sustained during com-
petition result in >7 days of absence, and about 20% resulted in 1–7 days of absence from
competition or training [2]. The treatment and rehabilitation processes have a significant
Copyright: © 2021 by the authors.
psychological and economic burden on the athlete, family, and society. It is extremely impor-
Licensee MDPI, Basel, Switzerland.
tant to implement preventive measures such as progressive training, protective equipment
This article is an open access article
distributed under the terms and
use, regulation of the competition rules, and nutrition in relation to the consequences of
conditions of the Creative Commons
injuries. Given that injuries are inevitable despite every precaution being taken, improving
Attribution (CC BY) license (https:// the treatment and rehabilitation process and thus decreasing the recovery time remains a
creativecommons.org/licenses/by/ fruitful area of research.
4.0/).

Nutrients 2022, 14, 53. https://doi.org/10.3390/nu14010053 https://www.mdpi.com/journal/nutrients


Nutrients 2022, 14, 53 2 of 20

Along with its effects on the physical and psychological health of the athlete, nutrition
is a pivotal factor affecting sports performance, the level of injury risk, and recovery time
from an injury. A significant body of scientific knowledge has been published on nutritional
strategies and ergogenic aids to improve sports performance [3–6]. However, limited
research is available about the role of nutrition in reducing the risk of injury and improving
the recovery process following injuries in athletes [7–11]. This is because, for athletes who
are intent on returning to their sport as quickly as possible, the uncertainties about injury
diagnosis and doubts regarding the efficacy of the treatment received are the main concerns
of such players. Hence, it is challenging to research such athletes. In recent years, several
review papers were published addressing the overall role of nutrition in injury prevention
and improving recovery [12–15]. Some review papers about this issue focused on specific
injuries or conditions such as muscle injuries [16–19], muscle damage [20], and muscle
disuse atrophy [21,22], while others focused on various sports branches such as track and
field [19,23], football [24], and soccer [19]. Since combat sports are popular all around
the world and about one-third of the injuries result in more than 7 days of absence from
competition or training, it is worth presenting the role of nutrition in injury prevention and
recovery. Therefore, the purpose of this review is to present various nutritional strategies
for reducing the risk of injury and improving the treatment and rehabilitation process
in combat sports. We will present the role of macro- and micronutrients, total energy
intake, and food supplements in the prevention and recovery time for injuries to skeletal
muscle, bone, tendons, and ligaments, as well as sports-related concussions (SRCs), the
most common injuries in combat sports. Furthermore, the injury risk associated with
weight cutting will be discussed along with how to reduce the potential risks. Finally,
nutritional considerations for returning to play after rehabilitation will be presented.

2. Injuries in Combat Sports


Numerous examples of research are available on the injury prevalence in various
combat sports such as wrestling [25–28], judo [29–31], taekwondo [32–37], boxing [38–42],
and karate [43–45], as well as comparisons of injury prevalence among Olympic combat
sports [2,46–48] and martial arts [1,49]. Due to the heterogeneity of these studies in terms
of participants (e.g., elite vs. amateur, children or adolescents vs. adults, and male vs.
female), injury definitions, surveillance methods (e.g., self-reporting, medical records, and
injury surveillance systems), and characteristics of the reported injuries (e.g., competition
injuries vs. training injuries and acute vs. chronic injuries), it is difficult to get an overall
view of the injury rate, type, location, and severity. The majority of the published studies
present data from the adult population and injuries that occurred during competition.
Fortunately, comprehensive findings were reported in a recent prospective cohort study
by Lystad et al. [2] that documented the incidence, severity, and profile of injury and the
risk factors for injury for Olympic combat sport athletes based on the data from the IOC
injury surveillance system and exposure data from official tournament records at three
consecutive Olympic Games: Beijing 2008, London 2012, and Rio de Janeiro 2016. In the
following sections, we outline a summary of the literature about the injury rate, injury
severity, locations, and tissues most frequently injured and the risk factors for injury in
Olympic combat sports.

2.1. Injury Rate


Olympic combat sport athletes (e.g., wrestling, judo, taekwondo, and boxing) sustain,
on average, one injury every 2.1 h of competition [2]. The injury rate per 1000 min of
exposure (IIRME ) is significantly lower in wrestling (4.8) compared with taekwondo (7.7),
boxing (9.2), and judo (9.6), with an overall injury rate of 7.8 [2]. A systematic review and
meta-analysis reported that karate athletes sustain, on average, 1 injury every 25 min of
competition and most of these injuries are minor or mild in severity [45]. Other reported
IIRME estimates in the literature for Olympic combat sports are 39.2 in karate [45], ranging
from 13.8 to 20.4 in boxing [40,50,51], 16.3 in taekwondo [34], 10.9 in judo [52], and 5.9
Nutrients 2022, 14, 53 3 of 20

in wrestling [53]. Jeong et al. [32] reported a 6.9 IIRME for new or recurrent injuries in
junior athletes during the 2018 World Taekwondo Junior Championships. Taekwondo was
listed within the top five most injurious sports in each of the Olympic games from 2008 to
2016 [54–56].

2.2. Injury Severity


According to the study by Lystad et al. [2], about 50% of injuries sustained during
competition result in at least 1 day of absence from training or competition. The proportion
of injuries leading to >7 days of absence from competition or training is higher in wrestling
(39.6%), judo (35.9%), and taekwondo (32.5%) than in boxing (21.0%) [2]. However, the
greatest injury burden risk was found in judo when both the incidence and severity were
taken into consideration [2]. The incidence rate for time-loss injuries in top-level karate ath-
letes was reported to be relatively low (10%) based on the data collected at four consecutive
World Karate Championships (2010, 2012, 2014, and 2016), and these injuries were due to
fractures (41%), dislocations (20%), or concussions (12%) [44].

2.3. Injury Location


Although the distribution of injury with respect to body location has great variability
across combat sports, the most frequently injured body regions are the head and neck
(35.9%), upper limbs (31.1%), and lower limbs (26.3%) [2]. Head and neck injuries are most
common in boxing (62.1%), upper limb injuries are frequently observed in judo (42.6%), and
lower limb injuries are frequent in taekwondo (59.5%) and wrestling (45.5%) [2]. Another
study by Lystad et al. [45] reported that the head and neck were the most commonly injured
body regions in Olympic-style karate (57.9%), while contusions (68.3%) and lacerations
(18.6%) were the most frequent injury types. According to a systematic review [46] based
on nine studies of Olympic combat sports, the most frequently injured areas were the head
and face (45.8%), wrist (12.0%), and lower back (7.8%) in boxing, the fingers (22.8%) and
thigh (9.1%) in taekwondo, the knee (24.8%), shoulder (17.8%), and head or face (16.6%)
in wrestling, and the lower back (10.9%), shoulder (10.2%), and knee (9.7%) in judo. In
junior taekwondo athletes, the most frequently reported injuries were contusions, ligament
ruptures and sprains, and lacerations and fractures to the lower extremities, head, and
trunk [32].

2.4. Injured Tissues


According to the data obtained at three consecutive Olympic Games (Beijing 2008,
London 2012, and Rio de Janeiro 2016), overall, the most commonly injured tissue types
in combat sports are superficial tissue and skin (42.9%), in addition to ligament and
joint capsule (31.4%) injuries [2]. Overall, joint sprains (31.4%) were the most frequent
injury type, followed by lacerations and abrasions (23.2%) and contusions (19.7%), while
concussions accounted for 3.2% of all recorded injuries [2]. Similarities and differences
exist in the distribution of injuries by pathology across combat sports. Contusions were
common in all combat sports (e.g., boxing: 18.5%; judo: 16.0%; taekwondo: 28.6%; and
wrestling: 21.8%). Lacerations were reported to be common in boxing (41.1%), while joint
sprains were predominant in judo (47.9%), taekwondo (33.3%), and wrestling (40.0%) [2].
Muscle injuries were most common in taekwondo (9.5%), followed by wrestling (9.1%),
boxing (5.6%), and judo (5.3%) [2]. Ligament or joint capsule injuries were most common
in judo (47.9%), followed by wrestling (40%), taekwondo (33.3%), and boxing (14.5%) [2].
Moreover, a high risk of mild traumatic brain injury (mTBI) or SRCs in combat sports
athletes, particularly wrestlers, was reported. As such, the mean annual incidence of mTBI
presented to emergency departments in the United States due to wrestling was significantly
higher (269.3 per 100,000 person-years) than boxing (85.6 per 100,000 person-years) and
martial arts (61.0 per 100,000 person-years) [48].
Nutrients 2022, 14, 53 4 of 20

2.5. Risk Factors for Injury


Gender, weight categories, training status, nutrition, wearing protective equipment,
and competition regulations are potential factors affecting injury risk in combat sports.
Injury risk was reported to be similar between genders and among weight categories
in Olympic combat sports. However, a higher IIRME was observed in athletes who lost
compared with their winning opponents [2]. Similarly, when adjusted for exposure time,
no significant difference in the injury rates was observed between males and females in
Olympic-style karate [45]. However, junior male taekwondo athletes incurred more injuries
than females, and contact between the athletes was reported to be the most common cause
of injury [32].

3. Injury Risk Associated with Rapid Weight Loss (RWL)


Combat athletes compete in specific weight categories to match competitors of similar
body weight, size, and strength [57,58]. Many combat athletes believe that by achiev-
ing rapid weight loss (RWL) a few days before weight categories are determined for
the competition, they gain an advantage over weaker competitors in terms of size and
strength [33,57,59]. For this purpose, they lose approximately 2–10% of their body weight
in the last 2–3 days before the competition [60]. RWL methods include severe limitation of
fluid and food intake, exercise with thermal clothing, sauna, diuretics, weight loss pills,
low-carb diets, laxatives, and vomiting [59,61,62]. All these methods may lead to several
health problems, an increased risk of injury, as well as a decrease in performance [60,61].
The list of health-related issues associated with RWL is long and includes both acute and
chronic effects. Interested readers may be referred to a recent review by Artioli et al. [60].
In brief, the most obvious consequences of RWL methods are dehydration and insuffi-
cient intake of nutrients, which in turn may lead to a decrease in blood plasma volume,
an increase in heart rate, impaired cardiac functions and thermoregulation, electrolyte
imbalances, low oxygen consumption, slowing of fluid passage through the kidneys, and
a decrease in glycogen stores [63,64]. In addition, RWL might result in hormonal imbal-
ance [65,66]. All of these altered physiological functions may increase the vulnerability of
the athletes to injury. Furthermore, RWL methods increase the risk of injury by negatively
affecting cognitive functions such as memory and concentration [29,58] and psychological
aspects [65,67]. For example, increased confusion, rage, fatigue, depression, and isolation,
as well as decreased short-term memory, vigour, concentration and self-esteem, have been
reported in athletes undergoing RWL practices [58,65]. All these psychological changes
may result in distractions, lack of control, aggressive behavior, difficulty in decision making,
and an inability to follow instructions during the match, all of which has the potential to
decrease performance and increase injury risk. Indeed, some epidemiological [68], as well
as experimental [69] data, show that RWL might increase the risk of injury. For instance,
Korean wrestlers had significantly higher injury rates during periods of RWL (23.18%) com-
pared with other training periods (11.93%) [70]. Most of the injuries occurred in the lower
extremities (38.0%), followed by upper extremity (25.9%), trunk (24.8%), and head and neck
injuries (11.3%). One study [70] reported major ligament-joint and muscle-tendon injuries
following RWL methods. In a study conducted with judokas [29], only 14% of the athletes
who did not use RWL methods were injured, while 48.7% of the judokas who applied RWL
were injured. Furthermore, a higher risk of injury was observed in athletes who lost 5 kg or
more of body weight [29]. In a case study, Oöpik et al. [69] reported that a 5–6% reduction
in body weight within 3 days affected wrestlers’ metabolisms and quadriceps femoris
muscle function, thus increasing the risk of injury. Similarly, Green et al. [29] reported a
higher probability of injury during competition in athletes who had lost more than 5% of
their body mass. Limited research is available [29,69,70] in the literature that examines the
relationship between RWL habits and the risk of injury. Thus, more research is needed on
this topic. Athletes should be advised to avoid RWL strategies to reduce the risk of injury.
Experts recommend that the use of RWL methods be banned because they meet all three of
the World Anti-Doping Agency (WADA)’s criteria for banning a substance or method from
Nutrients 2022, 14, 53 5 of 20

sports (potential to improve performance, potential health risk, and violation of the spirit
of sport) [60].

4. Nutrition in Muscle Injuries


Muscle injuries are one of the most common sports injuries, leading to decreased phys-
ical activity and immobilization, depending on the severity. In the following subheadings,
we present various nutritional and ergogenic support strategies to prevent muscle loss and
promote injury healing. In this respect, due to their therapeutic roles in preventing muscle
loss and anabolic resistance as well as promoting injury-healing amino acid and protein
intake, antioxidants, creatine, and omega-3 are given special attention.

4.1. Protein and Amino Acid Intake


Increasing protein intake during recovery is one of the first strategies in reducing
muscle loss and accelerating the healing process during the injury period [14]. In particular,
protein intake should be increased to prevent both muscle loss and anabolic resistance to
protein during immobilization after injury [22]. In this respect, the main considerations
are increasing daily protein intake in combination with exercise, balanced distribution of
protein intake during the day, and the amino acid content of protein. Increasing protein
intake to 2.3 g/kg/day is known to reduce muscle loss in states of negative energy bal-
ance [71]. For this reason, current daily protein intake recommendation (1.4 g/kg/day)
of combat athletes [72] can be increased during the injury period. On the other hand, it
should be noted that increasing protein intake to 1.6 g/kg/day in women on bed rest
for 60 days was shown not to prevent muscle loss, while a positive effect was observed
when combined with aerobic and resistance exercises [73]. Therefore, it is important to
emphasize that protein intake can prevent muscle loss, especially when combined with
exercise interventions during the rehabilitation process.
In addition to total protein intake, balanced distribution of the daily protein intake in
each meal is also important. For example, consumption of a moderate amount of protein
in each meal (breakfast: 31.5 ± 1.3 g, lunch: 29.9 ± 1.6 g, and dinner: 32.7 ± 1.6 g of
protein) stimulated 24-h muscle protein synthesis 25% more effectively than skewing the
protein intake toward the evening meal (breakfast: 10.7 ± 0.8 g, lunch:16.0 ± 0.5 g, and
dinner: 63.4 ± 3.7 g of protein) [74]. In another study, it was reported that consumption of
20–25 g (0.30 g/kg) provided more muscle protein synthesis compared with consumption
of 0, 5, and 10 g and similar to that for 40 g [75]. Thus, consuming such amounts of
protein intake (20–25 g/meal) should be recommended for healthy athletes. However, the
amount of protein in meals should also be increased for further protein synthesis during
the injury period. When increasing protein intake, the amino acid content should also be
considered. In particular, the amount of leucine, one of the keystones of protein synthesis,
is important [76], given that leucine helps anabolic stimulation by overcoming resistance to
protein synthesis. Indeed, leucine intake was reported to delay muscle loss in rats during
immobilization [77]. However, the effects of extra leucine intake in immobilized humans
are not incompletely explored. Additionally, future research is needed to determine the
amount of leucine to be consumed by athletes during the rehabilitation process.

4.2. Creatine
In addition to the well-documented effects of creatine, including improving strength,
increasing lean muscle mass, and helping the muscles recover more quickly during exercise,
creatine can also be beneficial in reducing muscle atrophy in athletes during immobilization
after injury [78]. For example, Hespel et al. [7] reported that consumption of creatine
monohydrate (from 20 g down to 5 g daily) in combination with rehabilitation exercises
for 10 weeks (3 days/week) accelerated muscle hypertrophy in disuse atrophy induced by
2 weeks of leg immobilization [7]. In another study, Op’t Eijnde et al. [9] investigated the ef-
fects of creatine monohydrate consumption on muscle glucose transporter type 4 (GLUT4)
levels during 2 weeks of immobilization and the following 10 weeks of rehabilitation train-
Nutrients 2022, 14, 53 6 of 20

ing with resistance exercises [9]. Creatine monohydrate consumption of 20 g/day during
the immobilization process attenuated the decrease in GLUT4 levels, and consumption of
creatine monohydrate during the training period (15 g for the first 3 weeks and 5 g for the
last 7 weeks) increased the GLUT4 levels by 40% [9]. Taken together, loading and mainte-
nance doses of creatine can be recommended during immobilization and rehabilitation for
the maintenance of muscle mass and metabolic health.

4.3. Omega-3
Recent research shows that fish oil plays a significant role in preventing muscle loss.
For example, the consumption of fish oil pills for 10 consecutive days in immobilized rats
alleviated muscle atrophy by stimulating the protein kinase B pathway in the immobilized
soleus muscle [79]. Intake of fish oil for 5 weeks also improved insulin sensitivity in muscle
protein metabolism in red angus [80]. However, no study to date has investigated whether
a similar beneficial effect of fish oil pills is evident in immobilized humans. Of the limited
studies, Smith et al. [81] reported increased anabolic responses to insulin and amino acids
following 8 weeks of omega-3 intake in healthy young and middle-aged individuals. In
physically active individuals, the consumption of 3900 mg fish oil (containing 3 g n-3) for
4 weeks decreased muscle damage [82]. Although fish oil consumption is promising in
reducing muscle loss due to muscle injuries, more studies involving human participants
are needed.

4.4. Antioxidants
Due to therapeutic roles in improving exercise-induced muscle damage, there has been
a significant scientific inquiry into antioxidants. In particular, antioxidants such as vitamins
C and E come to the fore in the fight against increased production of reactive oxygen species
after muscle injury [83]. However, there are contradictions in the literature regarding the
intake of antioxidants after muscle damage, as the therapeutic effects of antioxidants in
conditions such as inflammation, loss of strength, fatigue, and cell damage have not been
fully elucidated yet [84]. Moreover, some research reported increased muscle damage when
antioxidants were consumed following muscle damage due to the prevention of cellular
adaptation after exercise [85].
Taken together, although there is no study directly examining the effects of nutrition
on muscle injuries in combat sports, it is recommended to increase the daily protein and
leucine intake, consume creatine at a loading and maintenance dose, and intake omega-3
supplements to reduce muscle loss.

5. Nutrition in Joint, Connective Tissue, and Tendon Injuries


Joint, tendon, and connective tissue injuries are among the most frequent injuries
after superficial tissues and skin injuries in combat sports [2]. These injuries can impair
performance and lead to immobilization. The repair of joints, tendons, and ligaments is
not fully elucidated compared with muscle repair [86], yet current evidence suggests that
Collagen supplements and supplements that support collagen synthesis, such as gelatin
and vitamin C, are the most prominent strategies in these cases.

5.1. Collagen
Collagen, a connective tissue protein, is the primary component of tendons and
ligaments [87]. Collagen is rich in glycine, proline, hydroxylysine, and hydroxyproline,
and consumption of these amino acids increases collagen synthesis [88] as well as improves
the ligament–tendon structure [89,90]. Though collagen synthesis in tendons and muscles
is not affected by the increase in amino acid intake [91], consumption of an amino acid
content rich in proline, hydroxylysine, and hydroxyproline improves collagen synthesis [92].
Indeed, cell culture studies showed that hydrolyzed collagen significantly increases type
2 collagen biosynthesis as well as stimulates the regulation of the collagen cycle in cartilage
Nutrients 2022, 14, 53 7 of 20

tissue [93]. In an animal study, it was shown that oral intake of hydrolyzed type 1 collagen
peptides improved the size and composition of collagen fibrils in a tendon cell [94].
Collagen also plays a protective role in joint and connective tissue health, as well as
reducing joint pain. For example, consuming 25 mL of liquid collagen containing 10 g of
hydrolyzed collagen per day for 24 weeks improved joint health and reduced the risk of
joint degeneration and joint pain compared with a placebo [8]. In athletes with chronic ankle
injuries, significant reductions in the number of ankle injuries were observed following
ingestion of 5 g of collagen peptide for 6 months [11]. Collectively, intake of 10–15 g of
hydrolyzed collagen per day appears to be an effective strategy for the prevention and
treatment of joint, tendon, and ligament injuries.

5.2. Gelatin
Ample evidence shows that gelatin stimulates collagen synthesis. Gelatin, obtained
by boiling the skin, bones, tendons, and ligaments of animals such as cows, pigs, and fish,
has the same amino acid content as collagen [23,86]. Gelatin was reported to be beneficial
in collagen production and returning to the field from an injury [86]. For example, the
consumption of 15 g of gelatin 1 hour before a 6-min jump rope test performed to stimulate
collagen synthesis was shown to increase collagen synthesis twofold by raising the collagen-
1 amino terminal pro-peptide in the blood [95]. When the intake of 15 g of hydrolyzed
collagen and gelatin was compared in the same protocol, a similar positive effect was found
for the procollagen levels [96], suggesting positive and similar effects for the consumption
of 15 g of gelatin or hydrolyzed collagen 30–60 min before exercise [95,96].

5.3. Vitamin C
Consuming vitamin C together with collagen amino acids also improves collagen
synthesis [92,95]. Vitamin C is a pivotal player in collagen synthesis, and its deficiency
causes scurvy, which in turn results in collagen loss. Vitamin C is a cofactor of proline
4 hydroxylase, an enzyme involved in proline hydroxylation and procollagen synthesis
in connective tissues [97]. Furthermore, adequate vitamin C intake with collagen is of
significant importance given that vitamin C provides an increase in collagen synthesis,
tendon and ligament repair, and improvement in surgeries. At least 46 mg/day of vita-
min C intake is the minimal dose required to maintain collagen production [23], but the
effects of a higher intake on collagen synthesis remain to be determined. Citrus fruits,
strawberries, kiwi, peppers, and broccoli are some of the foods rich in vitamin C that
should be consumed [98]. Of the limited studies available, Shaw et al. [10] investigated the
effects of 24 weeks of evidence-based supplementation of gelatin (10 g/day) and vitamin
C (250 mg/day) along with creatine (loading: 20 g × 5 days immediately postoperative,
then 3 g/day) and leucine (3 g/day) on the leg strength and muscle mass in two elite rugby
union players with ruptured their left anterior cruciate ligaments, which were repaired
with traditional hamstring grafts. They reported that rehabilitation programs combined
with this type of nutrition strategy could attenuate leg strength loss due to 24 weeks of
physical inactivity. Among the very limited studies investigating the therapeutic role of
nutrition in joint, connective tissue, and tendon injuries, none were conducted with combat
athletes. However, the consumption of 10–15 g of collagen or gelatin containing vitamin
C following a joint-connective tissue injury is likely to provide significant support for the
prevention and treatment of these injuries.

6. Nutritional Strategies in Bone Injuries


Since combat sports involve striking, throwing, or immobilizing an opponent, the
main cause of injuries in combat athletes is mechanical energy leading to musculoskele-
tal injuries [2,99]. Studies reported that the proportion of fractures is greater in mixed
martial arts (27%), wrestling (21.3%), and kickboxing, in which fracture rates may reach
20% [100,101]. In addition, one of the most common bone injuries in athletes is stress frac-
tures, which are different from contact fractures [102]. Stress fractures are overuse injuries
Nutrients 2022, 14, 53 8 of 20

of the bone that result from the repeated application of stress lower than that required to
fracture the bone in a single loading session [103]. Although the pathophysiology of stress
fractures is not fully understood, it is considered to occur due in part to insufficient nutrient
intake [104].

6.1. Vitamin D and Calcium


Although there is a limited number of studies that investigated the association of
diet with prevention of or recovery from bone injuries, it is fairly well-known that diet
exerts a profound effect on bone health. For example, providing sufficient calcium and
vitamin D plays a significant role in optimal bone formation during healing from fractures.
Additionally, Barker et al. [105] reported an association of low vitamin D levels with
impaired recovery from knee surgery. It was demonstrated that if an individual has
sufficient vitamin D, supplementation may be detrimental, especially when used after a
bone fracture because certain macrophages might be suppressed [106]. Lappe et al. [107]
documented that supplementation with 800 IU/day of vitamin D and 2000 mg of calcium
reduced the risk of developing stress fractures in female navy recruits. However, an
excessive amount of micronutrient intake during recovery from injury remains a matter of
debate. Protein, magnesium, phosphorus, potassium, and fluoride play important roles in
bone health [108]. Iron, zinc, silicon, vitamin A, vitamin K, and vitamins C and B are other
nutrients supporting metabolic processes important for bone tissue [109,110]. From this
point of view, adequate intake of dairy products, fruits, and vegetables, specifically green
leafy vegetables, is beneficial a source for the main nutrients that support bone health.

6.2. Energy Intake


One of the more specific considerations in nutritional strategies for preventing bone
injuries in combat sports is RWL practices [58]. As discussed above, RWL practices may
impair athletes’ health in multiple ways. A common practice of RWL in weight-classed
athletes is to extremely reduce dietary intake, which might result in a hormonal imbal-
ance [65,66], which in turn acutely affects bone metabolism. Hence, there are concerns
that dietary strategies used by athletes to achieve RWL are very likely to lead to a low
energy availability (EA) state and nutrient deficiency, which are known to negatively affect
bone metabolism and increase the risk of bone injuries [111–113]. Low EA is a state of
insufficient energy intake to support the physiological functions required to maintain opti-
mal health [114], and it can be observed in both female and male athletes [112]. Ihle and
Loucks [115] reported that an energy intake under a threshold of 30 kcal/kg of fat-free mass
(FFM) daily results in disruptions in the hormonal markers of the reproductive system
and bone metabolism in females. Given that combat athletes lose weight several times
a year, their bone health will be negatively affected. Therefore, maintaining an EA of
45 kcal/kg/FFM per day is recommended in order to optimize bone health and prevent
bone injuries.
There has been an increase in the popularity of low-carbohydrate diets among athletes
in recent years [116]. This remains a matter of debate, as carbohydrate intake provides
the largest contribution to the daily total energy intake in the athlete’s diet. Nevertheless,
losing weight by manipulation of glycogen stores is a common method used among combat
athletes [61]. Furthermore, it is worth noting that these dietary approaches are likely to
increase the risk of a low-EA state due to carbohydrate restriction. Although some recent
data have shown that low carbohydrate availability might negatively affect bone health
independent of EA [117], more research is needed on this topic.

6.3. Protein Intake


Protein should be also considered when recovering from bone injuries. Athletes
are generally recommended to consume protein at a rate of more than 0.8 g/kg/body
mass daily [118]. Considering that protein is one of the key components in bone, it is
important for athletes to consume sufficient amounts of protein. On the other hand, some
Nutrients 2022, 14, 53 9 of 20

research suggested that high protein consumption could be detrimental to bone due to the
associated acidic load [119]. In contrast, recent meta-analyses that investigated the effect of
protein on bone health showed that there were no adverse effects of higher protein intake
on bone health [120,121]. Instead, there might be some beneficial effects on bone health,
particularly when combined with a sufficient calcium intake [23]. On the other hand, bone
collagen synthesis, an important factor for bone healing, responds to increased amino
acid levels [122]. Studies reported that protein supplementation enhanced recovery from
hip fracture surgery [123,124]. However, since these results are based on data obtained
from elderly subjects, further studies should investigate whether these effects of protein
supplementation are present in healthy athletes.

7. Nutrition in Sports-Related Concussions (SRCs)


SRCs are mild traumatic brain injuries (TBIs) global health concern and caused by
a biomechanical force to the body which causes temporary deterioration of neurological
functions [125]. TBIs are common in contact sports [126,127]. According to the position
statement released by the American Medical Society for Sports Medicine about concussions
in sports, protective equipment does not provide sufficient protection from the incidence
or severity of concussions in sports [128]. Hence, there is a need for divergent strategies
capable of preventing or reducing the deleterious effects of SRCs and subconcussive impacts.
From this point of view, nutritional supplementation could be valuable when provided
before and after TBIs, and this is a fruitful area of research for future studies.
Nutritional recommendations for TBIs are centered around antioxidants and anti-
inflammatory agents [125,129]. When a TBI is sustained, neuroinflammation and dysreg-
ulation of sodium (Na+ ), potassium (K+ ), and calcium (Ca2+ ) ions occur, and the influx
of Ca2+ ions leads to oxidative stress [130]. Curcumin, an anti-inflammatory compound,
was shown to be effective in reducing the levels of oxidized proteins and normalizing
brain-derived neurotrophic factor (BDNF) in rats following TBIs [131]. In addition, there
are many studies investigating the effects of n-3 fatty acids on TBIs [132–134]. Data from
animal studies demonstrated that supplementation of n-3 fatty acids decreased neuronal
damage and inflammation and normalized BDNF and neurotransmitter levels [132–134].
Although both n-3 fatty acids and curcumin seem to be effective in the treatment of TBIs,
solid recommendations cannot be made, and further human research is needed. A review
by Trojian et al. [129] suggested that lower serum levels of vitamins D, C, or E before
injury worsen the outcomes in animal studies and that caffeine intake after SRCs could be
detrimental. For a detailed discussion on nutritional supplements for the treatment and
prevention of SRCs, readers may be referred to the recent reviews by Trojian et al. [129] and
Lust et al. [125].

8. Preoperative Nutritional Strategies


Both the inflammatory response to the injury and surgical stress lead to catabolic reac-
tions [135]. The release of injury-induced stress hormones and proinflammatory cytokines
may sustain a prolonged catabolic state characterized by nitrogen loss [136] and insulin
resistance [135]. Hyperglycemia occurs despite elevated levels of insulin, exacerbating the
depletion of muscle protein [135]. Thus, adequate intake of macro- and micronutrients is
required to support this hypermetabolic state and the injury-healing process [12]. Tradi-
tionally, preoperative nutrition was mainly focused on recommendations about fasting and
restricted fluids beginning at midnight of the day of the operation [137]. An empty stomach
minimizes the risk of pulmonary aspiration. However, more recent data showed that these
fasting routines can be replaced with less strict ones without putting patients at risk [12,135].
Furthermore, providing high-carbohydrate beverages to patients immediately before oper-
ations was shown to be safe and to reduce the catabolic stress of surgery [138,139]. Indeed,
nutritional supplements known to support the immune system, which in turn diminishes
the catabolic response to operation and maximizes recovery potential, are safe for use
before surgery [12,138]. On the operation day, a liquid consisting of high molecular weight
Nutrients 2022, 14, 53 10 of 20

starch and essential amino acids is recommended 2 or 4 hours prior to surgery [12]. In
addition, given that midnight fasting results in significant depletion of the glycogen stores
known to increase the demand for amino acids, preoperative carbohydrate drinks may
reduce the risk of insulin resistance by maintaining and improving the whole-body protein
balance and muscle function [138].
Moreover, hyperglycemia may increase the risk of postoperative complications. In this
regard, a 100-g glucose intake with an oral solution the night before surgery and 50 g of
glucose 2 h before surgery were reported to reduce postoperative hyperglycemia [12,139]. In
addition, modified waxy maize starch could be used as a preoperation supplement to help
maintain glucose levels during surgery as well as to prevent postoperative hypoglycemia.
In summation, it is important for athletes to consume adequate complex carbohydrate
sources and proteins the night before surgery to minimize postoperative complications.

9. The Role of Nutrition in Returning to a Sport Following Injury


Injuries are prevalent in combat sports, and many injuries lead to time loss and
absence from sports, including both training and competing. The return of athletes to
sports following injury will depend on the injury classification and the cooperation of
different disciplines, including sports medicine, sport psychology, and sports nutrition.
Although nutritional interventions are often overlooked and not commonly a standard of
care in rehabilitation interventions, providing athletes with appropriate sports nutrition
consulting during the injury process is a pivotal factor that can augment the recovery
process and support healing. Hence, nutritional interventions should be coordinated with
the different phases of the recovery process to optimize the healing process. In this section,
we will focus on nutritional strategies that play important roles in the rehabilitation phase
for athletes following an injury.

9.1. Nutrition in Immobilization and Atrophy


Periods of immobilization caused by injuries are often associated with the loss of
muscle mass and strength, which are deleterious for health and performance [140,141].
Despite studies reporting muscle disuse atrophy following long experimental periods
ranging from 2 to as long as 17 weeks of bed rest or limb immobilization [142,143], some
studies reported profound impacts from only a few days of disuse on the skeletal muscle
mass and strength [141,144]. Therefore, muscle mass recovery following injury-induced
atrophy could be critical for combat athletes to accelerate a safe return to sports. Although
one of the best ways to recover muscle mass is exercise interventions (i.e., resistance
training), this is not always applicable. Therefore, reliable nutrition strategies can help to
limit muscle wasting and maintain muscle mass in these situations [145]. Indeed, adequate
total energy intake and appropriate dietary intake are the main nutritional strategies during
the rehabilitation of injured athletes, along with the intake of some supplements that have
the potential to help [23].
It is well-documented that muscle protein breakdown accelerates during injury re-
covery to support increased protein requirements due to wound healing and tissue re-
building [12,146]. However, optimizing healing is more dependent on the intake of protein
than the bodily breakdown of protein. Therefore, increasing dietary protein seems to be
an effective strategy during this process. Furthermore, given that the decrease in lean
body mass is of particular concern due to its role in all protein synthesis necessary for
healing, nutritional strategies, especially increasing protein intake, have key importance
both to increase lean body mass synthesis and to improve healing by increasing protein
synthesis [146]. However, research yielded equivocal results, with some studies reporting
benefits [147,148] while others reported no benefits [149,150]. For example, a recent system-
atic review by Pasiakos et al. [151] reported that protein supplementation did not enhance
the recovery of muscle function during recovery, suggesting that sufficient dietary protein
provided in the general diet of an athlete might be enough and with no additional protein
intake required to prevent muscle injury. It is noteworthy that despite the findings of this
Nutrients 2022, 14, 53 11 of 20

study, increased dietary protein is an adjunct therapy to attenuate muscle atrophy and
promote repair following an injury, which in turn accelerates a safe return to sports [23].
Collectively, injured athletes should consider maintaining protein intake to reduce muscle
mass loss during the healing process [152].
There are several other nutrients known to promote healing following an injury,
including vitamins C, D, and E, creatine, glycine, polyphenols, flavonoid, and branched-
chain amino acids (BCAAs). Although it is not fully explored, some researchers advocate
that vitamins C, D, and E work either by acting as an antioxidant or through a reduction
in inflammation [23]. For example, it was shown that vitamins C and E can decrease
recovery time, but it remains to be elucidated whether these vitamins can optimize the
healing process [153,154]. Research has also questioned whether increasing dietary glycine
could accelerate the healing of tendons in rats [155,156] and marathon runners [157]. The
findings showed that a diet containing 5% glycine, which is extremely high and not realistic
for consumption, increased collagen and mechanical strength in rats [155]. In contrast,
Buncman et al. [157] reported that 10 g of glycine supplementation (3 times/week for
2 weeks) did not heal skeletal muscle injuries in young male and female marathon runners.
The use of glycine in athletes following true injury has not been fully explored, and
therefore, clinical studies are needed for further insights. Moreover, although there was no
consensus reached [158], some studies reported that BCAAs such as leucine, isoleucine, and
valine can boost healing after a musculoskeletal injury as well as increase protein synthesis
and inhibit protein breakdown [159,160]. In particular, considering leucine is an essential
amino acid found in greater amounts in proteins and is required for optimal stimulation of
the rate of muscle protein synthesis [161], the ingestion of leucine in a mixture of essential
amino acids during healing can reverse an attenuated response of muscle protein synthesis.
However, given that there is little research in this area of sports nutrition, clinical studies are
needed to determine whether these supplement-based strategies can influence the recovery
process of injured athletes.

9.2. An Obvious Nutrient to Be Avoided after Injury: Alcohol


Large amounts of alcohol consumption after training and competition are part of
the social aspects of many sporting events [162]. Research has documented that it is
very likely that athletes consume alcohol above the threshold classified as hazardous
drinking [163,164]. Given that consumption of alcohol is associated with mental distress-
related factors [165], one can assume that sports competition and overwhelming training
periods might be a factor in the increasing consumption of alcohol among athletes through
the effect of these factors. Although many of the molecular processes disrupted by alcohol
are typically known, studies investigating the mechanisms of alcohol-induced tissue injury
are rare. A complete consideration of the literature is beyond the scope of this review.
Thus, interested readers are referred to other reviews [166,167]. Overall, as pointed out by
a review paper [13], alcohol is an obvious nutrient best avoided after injury. Accumulating
evidence shows that alcohol ingestion can impair muscle protein synthesis and wound
healing likely by reducing the inflammatory response [168–170] and can increase lean
body mass loss during immobilization [171]. It was also shown that alcohol ingestion
suppressed the elevated rates of muscle protein synthesis induced by exercise and protein
ingestion in young, active males [168] and the fracture repair process in rats [172]. Indeed,
alcohol consumption after exercise and injury is likely to have a detrimental effect on the
athlete’s recovery due to not eating or resting adequately as a result of intoxication [168,173].
Moreover, it is worth noting that increased blood flow to the injury site is likely to worsen
the severity of the injury and adversely affect the rate and outcome of healing. Therefore,
abstinence from alcohol consumption to limit blood flow to the site of the injury is routinely
advised due to the known vasodilatory effect of alcohol [167,173,174]. Taken together,
limited alcohol ingestion among athletes during the training period and healing process is
vital for a safe return to sports. The effects of alcohol on recovery and the time to return to
sports following injuries in athletes remains a fruitful area of investigation.
Nutrients 2022, 14, 53 12 of 20

9.3. Energy Intake Following Injury


The main goal during a phase of restricted training due to injury should be to maintain
physical capacity via sustaining cardiovascular capacity and muscle mass and minimization
of undesired body fat increases [175]. Following an injury, there is an inevitable reduction in
athletic activities, even if not stopped completely, to allow the injuries to recover, which in
turn results in reduced energy expenditure (EE). This reduction in EE consequently requires
a concomitant reduction in energy intake to prevent gains in body fat [23]. Considering
carbohydrates are an essential part of many athletes’ daily energy intake during hard train-
ing periods, it would be appropriate to reduce carbohydrate intake during inactivity [176].
However, it should be noted that there should not be a drastic reduction in energy intake
for injured athletes, since the healing process leads to a substantial increase in EE [177],
especially early and if the injury is severe (i.e., by up to as much as 50%) [13,178], depending
on the type and severity of the injury. In particular, the EE of athletes using crutches was re-
ported to increase two- to threefold [179]. Furthermore, given that performing some form of
exercise for the non-injured limb(s) is a common practice among athletes, a proper balance
between EE and energy intake during the healing period should be sought. Importantly,
energy intake during immobilization is known to exert a profound effect on muscle protein
synthesis [13]; that is, a negative energy balance would result in reduced muscle protein
synthesis and greater losses in functional strength and prolong the time before returning to
sports [12]. Therefore, maintaining an energy balance, specifically a high-protein intake,
is critical to attenuate the loss of lean body mass. Injured athletes can minimize weight
and fat gain while still meeting the nutritional needs of recovery with a diet including a
greater proportion of protein in combination with complex carbohydrates [12]. Although
weight and fat gain are the main concerns among athletes during the healing process, it
would be an appropriate strategy to maintain the macronutrient composition via a diet
with a 2:1 carbohydrate-to-protein ratio (e.g., 240 g of carbs and 120 g of protein), which
was shown to promote positive changes in body composition [180–182]. In this regard,
careful planning is needed to ensure that sufficient energy from macronutrient nutrition is
consumed during recovery from an injury.

10. Conclusions
Injuries will happen to athletes as an inevitable consequence of sports. In this regard,
nutrition solutions that can reduce the risk of injury, as well as decrease recovery time,
should be carefully implemented. Athletes should be encouraged to seek advice from expe-
rienced staff with up-to-date knowledge of nutritional strategies in the athletic population.
As a divergent field among sports disciplines, combat sports are contact sports involving
one-on-one combat that engage in full contact to score points, to cause an opponent to
submit, or to disable an opponent in a contest or match. Because of this nature, the risk of
injury is higher in combat sports (i.e., 7.8 injury/1000 min of exposure) compared with most
other sports. Therefore, providing evidence-based nutritional strategies that could reduce
the risk of injury as well as optimize the healing process is a pivotal factor for minimal risk
of injury and a safe return to sports. Furthermore, given that chronic low energy availability
is a major risk factor for bone injuries, athletes should maintain their energy balance such
that the energy intake (total kcal consumed) equals the EE (total kcal expended). Thus,
change in energy demands should be carefully monitored during the training, competition,
and recovery periods. Additionally, preventing RWL and consuming sufficient protein
are of significant importance for bone health, particularly in anabolic resistance in muscle
during combat sports. In addition to the protective effects of anabolic resistance, a sufficient
protein intake plays a primary role in the maintenance of lean muscle mass and is an
important predictor of muscle strength, power, balance, exercise tolerance, weakness, and
fatigue. In this respect, increasing the daily protein intake in combination with exercise,
balanced distribution of protein intake among meals, and consuming protein with a high
content of leucine will be effective strategies for optimal performance and recovery.
Nutrients 2022, 14, 53 13 of 20

In terms of the maintenance of muscle mass and metabolic health, creatine supplemen-
tation seems to improve strength and maintain lean muscle mass during the immobilization
and rehabilitation process. Moreover, although the published literature is not as abun-
dant for other supplements as for creatine, there is growing interest in the role of fish
oil consumption, calcium, and vitamin C, D, and E supplementation in reducing muscle
loss and inflammation associated with injuries during the recovery period. In addition,
vitamin C provides an increase in collagen synthesis, tendon and ligament repair, and
improvement in surgery outcomes. Thus, an adequate vitamin C intake (≥46 mg/day)
should be reached to maintain collagen production. Also, consuming hydrolyzed collagen
(10–15 g/day) is an effective strategy for the prevention and treatment of joint, tendon, and
ligament injuries. In particular, consumption of gelatin or hydrolyzed collagen 30–60 min
before exercise is beneficial for collagen production. Moreover, due to their role in reducing
oxidized proteins, neuronal damage, and inflammation as well as normalizing BDNF
and neurotransmitter levels in animal models, n-3 fatty acids and curcumin are likely to
be effective nutritional supplements during the healing process. Despite accumulating
evidence, however, more studies involving humans, specifically athlete populations, are
needed to better understand the possible benefits of these supplements for the prevention
of injury or recovery of injured athletes.
Notably, as a part of preoperative nutrition, it is important to provide athletes with an
adequate amount of macro- and micronutrients and nutritional supplements that support
the immune system. This will likely meet the demands of the catabolic state and contribute
to the injury-healing process. In this respect, consumption of complex carbohydrates and
proteins the night before surgery is recommended to minimize postoperative complications.
Additionally, alcohol ingestion should be limited due to its potential adverse effects on
muscle protein synthesis and wound healing, as well as weight gain and lean body mass
loss during immobilization. Considering the majority of the findings about the role of
nutrition in injury recovery come from animal studies or clinical human studies, further
high-quality studies, particularly from more diverse populations, specifically athletes,
are needed.

Author Contributions: Conceptualization, H.H.T., Ş.N.K., Y.G. and S.A.; investigation, H.H.T., Ş.N.K.,
Y.G. and S.A.; writing—original draft preparation, H.H.T., Ş.N.K., Y.G., S.A. and M.M.A.; writing—
review and editing, H.H.T. and Ş.N.K.; visualization, H.H.T.; supervision, H.H.T. and Ş.N.K. All
authors have read and agreed to the published version of the manuscript.
Funding: This research received no external funding.
Institutional Review Board Statement: Not applicable.
Informed Consent Statement: Not applicable.
Data Availability Statement: Not applicable.
Conflicts of Interest: The authors declare no conflict of interest.

References
1. Koutures, C.; Demorest, R.A. Participation and Injury in Martial Arts. Curr. Sports Med. Rep. 2018, 17, 433–438. [CrossRef]
2. Lystad, R.P.; Alevras, A.; Rudy, I.; Soligard, T.; Engebretsen, L. Injury incidence, severity and profile in Olympic combat sports: A
comparative analysis of 7712 athlete exposures from three consecutive Olympic Games. Br. J. Sports Med. 2020, 55, 1077–1083.
[CrossRef]
3. Reale, R.J.; Slater, G.; Burke, L.M. Individualised dietary strategies for Olympic combat sports: Acute weight loss, recovery and
competition nutrition. Eur. J. Sport Sci. 2017, 17, 727–740. [CrossRef]
4. Peeling, P.; Binnie, M.; Goods, P.; Sim, M.; Burke, L.M. Evidence-Based Supplements for the Enhancement of Athletic Performance.
Int. J. Sport Nutr. Exerc. Metab. 2018, 28, 178–187. [CrossRef]
5. Close, G.; Hamilton, D.; Philp, A.; Burke, L.M.; Morton, J. New strategies in sport nutrition to increase exercise performance. Free
Radic. Biol. Med. 2016, 98, 144–158. [CrossRef] [PubMed]
6. Thomas, D.T.; Erdman, K.A.; Burke, L.M. Position of the Academy of Nutrition and Dietetics, Dietitians of Canada, and the
American College of Sports Medicine: Nutrition and Athletic Performance. J. Acad. Nutr. Diet. 2016, 116, 501–528. [CrossRef]
Nutrients 2022, 14, 53 14 of 20

7. Hespel, P.; Eijnde, B.O.; Van Leemputte, M.; Ursø, B.; Greenhaff, P.; Labarque, V.; Dymarkowski, S.; Van Hecke, P.; Richter, E.A.
Oral creatine supplementation facilitates the rehabilitation of disuse atrophy and alters the expression of muscle myogenic factors
in humans. J. Physiol. 2001, 536, 625–633. [CrossRef] [PubMed]
8. Clark, K.L.; Sebastianelli, W.; Flechsenhar, K.R.; Aukermann, D.F.; Meza, F.; Millard, R.L.; Deitch, J.R.; Sherbondy, P.S.; Albert, A.
24-Week study on the use of collagen hydrolysate as a dietary supplement in athletes with activity-related joint pain. Curr. Med.
Res. Opin. 2008, 24, 1485–1496. [CrossRef] [PubMed]
9. Op’t Eijnde, B.; Ursø, B.; Richter, E.A.; Greenhaff, P.L.; Hespel, P. Effect of oral creatine supplementation on human muscle GLUT4
protein content after immobilization. Diabetes 2001, 50, 18–23. [CrossRef] [PubMed]
10. Shaw, G.; Serpell, B.; Baar, K. Rehabilitation and nutrition protocols for optimising return to play from traditional ACL recon-
struction in elite rugby union players: A case study. J. Sports Sci. 2019, 37, 1794–1803. [CrossRef]
11. Dressler, P.; Gehring, D.; Zdzieblik, D.; Oesser, S.; Gollhofer, A.; König, D. Improvement of Functional Ankle Properties Following
Supplementation with Specific Collagen Peptides in Athletes with Chronic Ankle Instability. J. Sports Sci. Med. 2018, 17, 298–304.
[CrossRef]
12. Smith-Ryan, A.E.; Hirsch, K.R.; Saylor, H.E.; Gould, L.M.; Blue, M.N.M. Nutritional Considerations and Strategies to Facilitate
Injury Recovery and Rehabilitation. J. Athl. Train. 2020, 55, 918–930. [CrossRef]
13. Tipton, K.D. Nutritional Support for Exercise-Induced Injuries. Sports Med. 2015, 45 (Suppl. 1), 93–104. [CrossRef] [PubMed]
14. Tipton, K.D. Nutrition for Acute Exercise-Induced Injuries. Ann. Nutr. Metab. 2010, 57 (Suppl. 2), 43–53. [CrossRef] [PubMed]
15. Papadopoulou, S.K. Rehabilitation Nutrition for Injury Recovery of Athletes: The Role of Macronutrient Intake. Nutrients 2020,
12, 2449. [CrossRef] [PubMed]
16. Vergara-Gutiérrez, L.; Lizárraga-Dallo, A.; Pruna-Grive, R. Nutritional Intervention during Muscle Injury Considering its
Pathophysiology. Apunts. Educ. Fís. Deportes 2020, 142, 8–20.
17. Quintero, K.J.; Resende, A.D.S.; Leite, G.S.F.; Junior, A.H.L. An overview of nutritional strategies for recovery process in
sports-related muscle injuries. Nutrire 2018, 43, 27. [CrossRef]
18. Bloomer, R.J. The Role of Nutritional Supplements in the Prevention and Treatment of Resistance Exercise-Induced Skeletal
Muscle Injury. Sports Med. 2007, 37, 519–532. [CrossRef]
19. Rollo, I.; Carter, J.M.; Close, G.L.; Yangüas, J.; Gomez-Diaz, A.; Leal, D.M.; Duda, J.L.; Holohan, D.; Erith, S.J.; Podlog, L. Role of
sports psychology and sports nutrition in return to play from musculoskeletal injuries in professional soccer: An interdisciplinary
approach. Eur. J. Sport Sci. 2021, 21, 1054–1063. [CrossRef]
20. Sousa, M.; Teixeira, V.H.; Soares, J. Dietary strategies to recover from exercise-induced muscle damage. Int. J. Food Sci. Nutr. 2014,
65, 151–163. [CrossRef]
21. Wall, B.T.; van Loon, L.J. Nutritional strategies to attenuate muscle disuse atrophy. Nutr. Rev. 2013, 71, 195–208. [CrossRef]
22. Wall, B.T.; Morton, J.P.; Van Loon, L.J.C. Strategies to maintain skeletal muscle mass in the injured athlete: Nutritional considera-
tions and exercise mimetics. Eur. J. Sport Sci. 2015, 15, 53–62. [CrossRef]
23. Close, G.L.; Sale, C.; Baar, K.; Bermon, S. Nutrition for the Prevention and Treatment of Injuries in Track and Field Athletes. Int. J.
Sport Nutr. Exerc. Metab. 2019, 29, 189–197. [CrossRef] [PubMed]
24. Medina, D.; Lizarraga, A.; Drobnick, F. Injury prevention and nutrition in football. Sports Sci. Exch. 2014, 27, 1–5.
25. Halloran, L. Wrestling injuries. Orthop. Nurs. 2008, 27, 189–192. [CrossRef] [PubMed]
26. Hewett, T.E.; Pasque, C.; Heyl, R.; Wroble, R. Wrestling injuries. Med. Sports Sci. 2005, 48, 152–178.
27. Thomas, R.E.; Zamanpour, K. lnjuries in wrestling: Systematic review. Phys. Sportsmed. 2018, 46, 168–196. [CrossRef] [PubMed]
28. Nomoto, J.; Seiki, Y.; Nemoto, M.; Takahashi, H.; Terashima, H.; Yokota, K.; Kondo, K.; Kano, T.; Goto, S.; Sugo, N. Head Trauma
in Female Professional Wrestlers. Neurol. Med. Chir. 2007, 47, 147–152. [CrossRef]
29. Green, C.M.; Petrou, M.J.; Fogarty-Hover, M.L.S.; Rolf, C.G. Injuries among judokas during competition. Scand. J. Med. Sci. Sports
2007, 17, 205–210. [CrossRef]
30. Koshida, S.; Deguchi, T.; Miyashita, K.; Iwai, K.; Urabe, Y. The common mechanisms of anterior cruciate ligament injuries in judo:
A retrospective analysis. Br. J. Sports Med. 2010, 44, 856–861. [CrossRef] [PubMed]
31. Pocecco, E.; Ruedl, G.; Stankovic, N.; Sterkowicz, S.; Del Vecchio, F.B.; García, C.G.; Rousseau, R.; Wolf, M.; Kopp, M.;
Miarka, B.; et al. Injuries in judo: A systematic literature review including suggestions for prevention. Br. J. Sports Med. 2013, 47,
1139–1143. [CrossRef] [PubMed]
32. Jeong, H.S.; Ha, S.; Jeong, D.H.; O’Sullivan, D.M.; Lee, S.Y. Injury and Illness in World Taekwondo Junior Athletes: An
Epidemiological Study. Int. J. Environ. Res. Public Health 2021, 18, 2134. [CrossRef]
33. Kazemi, M.; Shearer, H.; Choung, Y.S. Pre-competition habits and injuries in Taekwondo athletes. BMC Musculoskelet. Disord.
2005, 6, 1–9. [CrossRef]
34. Lystad, R.P.; Graham, P.L.; Poulos, R.G. Exposure-adjusted incidence rates and severity of competition injuries in Australian
amateur taekwondo athletes: A 2-year prospective study. Br. J. Sports Med. 2013, 47, 441–446. [CrossRef] [PubMed]
35. Lystad, R.P.; Pollard, H.; Graham, P.L. Epidemiology of injuries in competition taekwondo: A meta-analysis of observational
studies. J. Sci. Med. Sport 2009, 12, 614–621. [CrossRef]
36. Lystad, R.P.; Swain, M.; Graham, P. Risk factors for injury in Olympic-style competition taekwondo: A systematic review. J. Sports
Med. Phys. Fit. 2013, 53, 655–664.
Nutrients 2022, 14, 53 15 of 20

37. Pieter, W.; Fife, G.P.; O’Sullivan, D.M. Competition injuries in taekwondo: A literature review and suggestions for prevention and
surveillance. Br. J. Sports Med. 2012, 46, 485–491. [CrossRef]
38. Loosemore, M.; Knowles, C.H.; Whyte, G.P. Amateur boxing and risk of chronic traumatic brain injury: Systematic review of
observational studies. BMJ 2007, 335, 809. [CrossRef]
39. Loosemore, M.; Lightfoot, J.; Beardsley, C. Boxing injuries by anatomical location: A systematic review. Med. Sport. J. Rom. Sports
Med. Soc. 2015, 11, 2583.
40. Loosemore, M.; Lightfoot, J.; Palmer-Green, D.; Gatt, I.; Bilzon, J.; Beardsley, C. Boxing injury epidemiology in the Great Britain
team: A 5-year surveillance study of medically diagnosed injury incidence and outcome. Br. J. Sports Med. 2015, 49, 1100–1107.
[CrossRef] [PubMed]
41. Siewe, J.; Rudat, J.; Zarghooni, K.; Sobottke, R.; Eysel, P.; Herren, C.; Knoll, P.; Illgner, U.; Michael, J. Injuries in Competitive
Boxing. A Prospective Study. Int. J. Sports Med. 2015, 36, 249–253. [CrossRef]
42. Zazryn, T.R.; McCrory, P.R.; Cameron, P.A. Neurologic Injuries in Boxing and Other Combat Sports. Neurol. Clin. 2008, 26,
257–270. [CrossRef] [PubMed]
43. Thomas, R.E.; Ornstein, J. Injuries in karate: Systematic review. Phys. Sportsmed. 2018, 46, 279–303. [CrossRef]
44. Augustovičová, D.; Lystad, R.P.; Arriaza, R. Time-Loss Injuries in Karate: A Prospective Cohort Study of 4 Consecutive World
Karate Championships. Orthop. J. Sports Med. 2019, 7, 2325967119865866. [CrossRef]
45. Lystad, R.P.; Augustovičová, D.; Harris, G.; Beskin, K.; Arriaza, R. Epidemiology of injuries in Olympic-style karate competitions:
Systematic review and meta-analysis. Br. J. Sports Med. 2020, 54, 976–983. [CrossRef] [PubMed]
46. Bromley, S.J.; Drew, M.K.; Talpey, S.; McIntosh, A.S.; Finch, C.F. A systematic review of prospective epidemiological research into
injury and illness in Olympic combat sport. Br. J. Sports Med. 2018, 52, 8–16. [CrossRef]
47. Noh, J.-W.; Park, B.-S.; Kim, M.-Y.; Lee, L.-K.; Yang, S.-M.; Lee, W.-D.; Shin, Y.-S.; Kim, J.-H.; Lee, J.-U.; Kwak, T.-Y.; et al. Analysis
of combat sports players’ injuries according to playing style for sports physiotherapy research. J. Phys. Ther. Sci. 2015, 27,
2425–2430. [CrossRef] [PubMed]
48. Lemme, N.J.; Johnston, B.; DeFroda, S.F.; Owens, B.D.; Kriz, P.K. Incidence of Combat Sport-Related Mild Traumatic Brain Injuries
Presenting to the Emergency Department From 2012 to 2016. Clin. J. Sport Med. 2018. [CrossRef]
49. Thomas, R.E.; Thomas, B.C. Systematic review of injuries in mixed martial arts. Phys. Sportsmed. 2018, 46, 155–167. [CrossRef]
50. Porter, M.; O’brie’n, M. Incidence and Severity of Injuries Resulting From Amateur Boxing in Ireland. Clin. J. Sport Med. 1996, 6,
97–101. [CrossRef]
51. Zazryn, T.; Cameron, P.; McCrory, P. A prospective cohort study of injury in amateur and professional boxing. Br. J. Sports Med.
2006, 40, 670–674. [CrossRef] [PubMed]
52. Cierna, D.; Štefanovský, M.; Matejová, L.; Lystad, R.P. Epidemiology of Competition Injuries in Elite European Judo Athletes: A
Prospective Cohort Study. Clin. J. Sport Med. 2019, 29, 336–340.
53. Strauss, R.H.; Lanese, R.R. Injuries among wrestlers in school and college tournaments. JAMA 1982, 248, 2016–2019. [CrossRef]
[PubMed]
54. Engebretsen, L.; Soligard, T.; Steffen, K.; Alonso, J.M.; Aubry, M.; Budgett, R.; Dvorak, J.; Jegathesan, M.; Meeuwisse, W.H.;
Mountjoy, M.; et al. Sports injuries and illnesses during the London Summer Olympic Games 2012. Br. J. Sports Med. 2013, 47,
407–414. [CrossRef] [PubMed]
55. Junge, A.; Engebretsen, L.; Mountjoy, M.L.; Alonso, J.M.; Renström, P.A.F.H.; Aubry, M.J.; Dvorak, J. Sports Injuries During the
Summer Olympic Games 2008. Am. J. Sports Med. 2009, 37, 2165–2172. [CrossRef] [PubMed]
56. Soligard, T.; Steffen, K.; Palmer, D.; Alonso, J.M.; Bahr, R.; Lopes, A.; Dvorak, J.; Grant, M.-E.; Meeuwisse, W.; Mountjoy, M.; et al.
Sports injury and illness incidence in the Rio de Janeiro 2016 Olympic Summer Games: A prospective study of 11274 athletes
from 207 countries. Br. J. Sports Med. 2017, 51, 1265–1271. [CrossRef]
57. Langan-Evans, C.; Close, G.L.; Morton, J.P. Making Weight in Combat Sports. Strength Cond. J. 2011, 33, 25–39. [CrossRef]
58. Franchini, E.; Brito, C.J.; Artioli, G.G. Weight loss in combat sports: Physiological, psychological and performance effects. J. Int.
Soc. Sports Nutr. 2012, 9, 52. [CrossRef]
59. Artioli, G.G.; Scagliusi, F.; Kashiwagura, D.; Franchini, E.; Gualano, B.; Junior, A.L. Development, validity and reliability of a
questionnaire designed to evaluate rapid weight loss patterns in judo players. Scand. J. Med. Sci. Sports 2010, 20, e177–e187.
[CrossRef]
60. Artioli, G.G.; Saunders, B.; Iglesias, R.T.; Franchini, E. It is Time to Ban Rapid Weight Loss from Combat Sports. Sports Med. 2016,
46, 1579–1584. [CrossRef] [PubMed]
61. Reale, R.; Slater, G.; Burke, L.M. Acute-Weight-Loss Strategies for Combat Sports and Applications to Olympic Success. Int. J.
Sports Physiol. Perform. 2017, 12, 142–151. [CrossRef]
62. Steen, S.N.; Brownell, K.D. Patterns of weight loss and regain in wrestlers: Has the tradition changed? Med. Sci. Sports Exerc.
1990, 22, 762–768. [CrossRef]
63. Fogelholm, M. Effects of Bodyweight Reduction on Sports Performance. Sports Med. 1994, 18, 249–267. [CrossRef] [PubMed]
64. Oppliger, R.A.; Case, H.S.; A Horswill, C.; Landry, G.L.; Shelter, A.C. American College of Sports Medicine position stand. Weight
loss in wrestlers. Med. Sci. Sports Exerc. 1996, 28, ix–xii. [CrossRef]
65. Degoutte, F.; Jouanel, P.; Bègue, R.J.; Colombier, M.; Lac, G.; Pequignot, J.M.; Filaire, E. Food Restriction, Performance, Biochemical,
Psychological, and Endocrine Changes in Judo Athletes. Endoscopy 2006, 27, 9–18. [CrossRef]
Nutrients 2022, 14, 53 16 of 20

66. Roemmich, J.N.; Sinning, W.E. Weight loss and wrestling training: Effects on growth-related hormones. J. Appl. Physiol. 1997, 82,
1760–1764. [CrossRef] [PubMed]
67. Lakicevic, N.; Roklicer, R.; Bianco, A.; Mani, D.; Paoli, A.; Trivic, T.; Ostojic, S.M.; Milovancev, A.; Maksimovic, N.; Drid, P. Effects
of Rapid Weight Loss on Judo Athletes: A Systematic Review. Nutrients 2020, 12, 1220. [CrossRef]
68. Agel, J.; Ransone, J.; Dick, R.; Oppliger, R.; Marshall, S.W. Descriptive epidemiology of collegiate men’s wrestling injuries:
National Collegiate Athletic Association Injury Surveillance System, 1988–1989 through 2003–2004. J. Athl. Train. 2007, 42, 303.
69. Ööpik, V.; Pääsuke, M.; Sikku, T.; Timpmann, S.; Medijainen, L.; Ereline, J.; Smirnova, T.; Gapejeva, E. Effect of rapid weight loss
on metabolism and isokinetic performance capacity. A case study of two well trained wrestlers. J. Sports Med. Phys. Fit. 1996, 36,
127–131.
70. Kim, J.C.; Park, K.J. Injuries and rapid weight loss in elite Korean wrestlers: An epidemiological study. Phys. Sportsmed. 2021, 49,
308–315. [CrossRef] [PubMed]
71. Mettler, S.; Mitchell, N.; Tipton, K. Increased Protein Intake Reduces Lean Body Mass Loss during Weight Loss in Athletes. Med.
Sci. Sports Exerc. 2010, 42, 326–337. [CrossRef] [PubMed]
72. Pettersson, S.; Berg, C.M. Dietary Intake at Competition in Elite Olympic Combat Sports. Int. J. Sport Nutr. Exerc. Metab. 2014, 24,
98–109. [CrossRef] [PubMed]
73. Trappe, T.A.; Burd, N.A.; Louis, E.S.; Lee, G.A.; Trappe, S.W. Influence of concurrent exercise or nutrition countermeasures
on thigh and calf muscle size and function during 60 days of bed rest in women. Acta Physiol. 2007, 191, 147–159. [CrossRef]
[PubMed]
74. Mamerow, M.M.; Mettler, J.A.; English, K.L.; Casperson, S.; Arentson-Lantz, E.; Sheffield-Moore, M.; Layman, D.; Paddon-Jones,
D. Dietary Protein Distribution Positively Influences 24-h Muscle Protein Synthesis in Healthy Adults. J. Nutr. 2014, 144, 876–880.
[CrossRef]
75. Moore, D.R.; Robinson, M.J.; Fry, J.L.; Tang, J.E.; Glover, E.I.; Wilkinson, S.B.; Prior, T.; Tarnopolsky, M.A.; Phillips, S.M. Ingested
protein dose response of muscle and albumin protein synthesis after resistance exercise in young men. Am. J. Clin. Nutr. 2009, 89,
161–168. [CrossRef]
76. Anthony, J.C.; Anthony, T.G.; Layman, D.K. Leucine supplementation enhances skeletal muscle recovery in rats following exercise.
J. Nutr. 1999, 129, 1102–1106. [CrossRef] [PubMed]
77. Baptista, I.L.; Leal, M.L.; Artioli, G.G.; Aoki, M.S.; Fiamoncini, J.; Turri, A.O.; Curi, R.; Miyabara, E.H.; Moriscot, A.S. Leucine
attenuates skeletal muscle wasting via inhibition of ubiquitin ligases. Muscle Nerve 2010, 41, 800–808. [CrossRef] [PubMed]
78. Hespel, P.; Derave, W. Ergogenic effects of creatine in sports and rehabilitation. Subcell Biochem. 2007, 46, 246–259. [CrossRef]
79. You, J.-S.; Park, M.-N.; Song, W.; Lee, Y.-S. Dietary fish oil alleviates soleus atrophy during immobilization in association with Akt
signaling to p70s6k and E3 ubiquitin ligases in rats. Appl. Physiol. Nutr. Metab. 2010, 35, 310–318. [CrossRef]
80. Gingras, A.A.; White, P.J.; Chouinard, P.Y.; Julien, P.; Davis, T.A.; Dombrowski, L.; Couture, Y.; Dubreuil, P.; Myre, A.;
Bergeron, K.; et al. Long-chain omega-3 fatty acids regulate bovine whole-body protein metabolism by promoting muscle
insulin signalling to the Akt-mTOR-S6K1 pathway and insulin sensitivity. J. Physiol. 2007, 579, 269–284. [CrossRef]
81. Smith, G.I.; Atherton, P.; Reeds, D.N.; Mohammed, B.S.; Rankin, D.; Rennie, M.J.; Mittendorfer, B. Omega-3 polyunsaturated
fatty acids augment the muscle protein anabolic response to hyperinsulinaemia–hyperaminoacidaemia in healthy young and
middle-aged men and women. Clin. Sci. 2011, 121, 267–278. [CrossRef]
82. Kyriakidou, Y.; Wood, C.; Ferrier, C.; Dolci, A.; Elliott, B. The effect of Omega-3 polyunsaturated fatty acid supplementation on
exercise-induced muscle damage. J. Int. Soc. Sports Nutr. 2021, 18, 1–11. [CrossRef]
83. Powers, S.K.; DeRuisseau, K.C.; Quindry, J.; Hamilton, K.L. Dietary antioxidants and exercise. J. Sports Sci. 2004, 22, 81–94.
[CrossRef] [PubMed]
84. D’Antona, G. Nutritional Interventions as Potential Strategy to Minimize Exercise-Induced Muscle Injuries in Sports. Muscle Inj.
Sport Med. 2013, 63, 93. [CrossRef]
85. Teixeira, V.H.; Valente, H.F.; Casal, S.I.; Marques, A.F.; Moreira, P.A. Antioxidants Do Not Prevent Postexercise Peroxidation and
May Delay Muscle Recovery. Med. Sci. Sports Exerc. 2009, 41, 1752–1760. [CrossRef]
86. Baar, K. Minimizing Injury and Maximizing Return to Play: Lessons from Engineered Ligaments. Sports Med. 2017, 47 (Suppl. 1),
5–11. [CrossRef]
87. Mienaltowski, M.J.; Birk, D.E. Structure, Physiology, and Biochemistry of Collagens. Adv. Exp. Med. Biol. 2014, 802, 5–29.
[CrossRef] [PubMed]
88. Smith, K.; Rennie, M.J. New approaches and recent results concerning human-tissue collagen synthesis. Curr. Opin. Clin. Nutr.
Metab. Care 2007, 10, 582–590. [CrossRef] [PubMed]
89. Zhang, G.; Young, B.B.; Ezura, Y.; Favata, M.; Soslowsky, L.J.; Chakravarti, S.; E Birk, D. Development of tendon structure and
function: Regulation of collagen fibrillogenesis. J. Musculoskelet. Neuronal Interact. 2005, 5, 5–21. [PubMed]
90. Banos, C.C.; Thomas, A.H.; Kuo, C.K. Collagen fibrillogenesis in tendon development: Current models and regulation of fibril
assembly. Birth Defects Res. Part C Embryo Today Rev. 2008, 84, 228–244. [CrossRef]
91. Babraj, J.; Cuthbertson, D.J.R.; Smith, K.; Langberg, H.; Miller, B.; Krogsgaard, M.R.; Kjaer, M.; Rennie, M.J. Collagen synthesis in
human musculoskeletal tissues and skin. Am. J. Physiol. Metab. 2005, 289, E864–E869. [CrossRef]
92. Paxton, J.Z.; Grover, L.M.; Baar, K. Engineering anIn VitroModel of a Functional Ligament from Bone to Bone. Tissue Eng. Part A
2010, 16, 3515–3525. [CrossRef] [PubMed]
Nutrients 2022, 14, 53 17 of 20

93. Oesser, S.; Seifert, J. Stimulation of type II collagen biosynthesis and secretion in bovine chondrocytes cultured with degraded
collagen. Cell Tissue Res. 2003, 311, 393–399. [CrossRef] [PubMed]
94. Minaguchi, J.; Koyama, Y.-I.; Meguri, N.; Hosaka, Y.; Ueda, H.; Kusubata, M.; Hirota, A.; Irie, S.; Mafune, N.; Takehana, K. Effects
of Ingestion of Collagen Peptide on Collagen Fibrils and Glycosaminoglycans in Achilles Tendon. J. Nutr. Sci. Vitaminol. 2005, 51,
169–174. [CrossRef] [PubMed]
95. Shaw, G.; Lee-Barthel, A.; Ross, M.L.; Wang, B.; Baar, K. Vitamin C–enriched gelatin supplementation before intermittent activity
augments collagen synthesis. Am. J. Clin. Nutr. 2017, 105, 136–143. [CrossRef] [PubMed]
96. Lis, D.M.; Baar, K. Effects of Different Vitamin C–Enriched Collagen Derivatives on Collagen Synthesis. Int. J. Sport Nutr. Exerc.
Metab. 2019, 29, 526–531. [CrossRef]
97. Peterkofsky, B. Ascorbate requirement for hydroxylation and secretion of procollagen: Relationship to inhibition of collagen
synthesis in scurvy. Am. J. Clin. Nutr. 1991, 54 (Suppl. 6), 1135S–1140S. [CrossRef]
98. Kloubec, J.; Harris, C. Whole Foods Nutrition for Enhanced Injury Prevention and Healing. ACSMs Health Fit. J. 2016, 20, 7–11.
[CrossRef]
99. McPherson, M.; Pickett, W. Characteristics of martial art injuries in a defined Canadian population: A descriptive epidemiological
study. BMC Public Health 2010, 10, 795. [CrossRef]
100. Lystad, R.P. Epidemiology of injuries in full-contact combat sports. Australas Epidemiol. 2015, 22, 14–18.
101. Zazryn, T.R.; Finch, C.F.; McCrory, P. A 16 year study of injuries to professional boxers in the state of Victoria, Australia. Br. J.
Sports Med. 2003, 37, 321–324. [CrossRef] [PubMed]
102. Fredericson, M.; Jennings, F.; Beaulieu, C.; Matheson, G.O. Stress Fractures in Athletes. Top. Magn. Reson. Imaging 2006, 17,
309–325. [CrossRef] [PubMed]
103. Brukner, P.; Bradshaw, C.; Khan, K.M.; White, S.; Crossley, K. Stress fractures: A review of 180 cases. Clin. J. Sport Med. 1996, 6,
85–89. [CrossRef] [PubMed]
104. Moran, D.S.; Heled, Y.; Arbel, Y.; Israeli, E.; Finestone, A.S.; Evans, R.K.; Yanovich, R. Dietary intake and stress fractures among
elite male combat recruits. J. Int. Soc. Sports Nutr. 2012, 9, 6. [CrossRef] [PubMed]
105. Barker, T.; Martins, T.B.; Hill, H.R.; Kjeldsberg, C.R.; Trawick, R.H.; Weaver, L.K.; Traber, M. Low Vitamin D Impairs Strength
Recovery After Anterior Cruciate Ligament Surgery. J. Evid.-Based Integr. Med. 2011, 16, 201–209. [CrossRef]
106. Ljungqvist, O.; Søreide, E. Preoperative fasting. J. Br. Surg. 2003, 90, 400–406. [CrossRef]
107. Lappe, J.; Cullen, D.; Haynatzki, G.; Recker, R.; Ahlf, R.; Thompson, K. Calcium and Vitamin D Supplementation Decreases
Incidence of Stress Fractures in Female Navy Recruits. J. Bone Miner. Res. 2008, 23, 741–749. [CrossRef] [PubMed]
108. Palacios, C. The role of nutrients in bone health, from A to Z. Crit. Rev. Food Sci. Nutr. 2006, 46, 621–628. [CrossRef]
109. Price, C.T.; Langford, J.R.; A Liporace, F. Essential Nutrients for Bone Health and a Review of their Availability in the Average
North American Diet. Open Orthop. J. 2012, 6, 143–149. [CrossRef]
110. Sale, C.; Elliott-Sale, K.J. Nutrition and Athlete Bone Health. Sports Med. 2019, 49, 139–151. [CrossRef]
111. Heikura, I.A.; Uusitalo, A.L.T.; Stellingwerff, T.; Bergland, D.; Mero, A.A.; Burke, L.M. Low Energy Availability Is Difficult to
Assess but Outcomes Have Large Impact on Bone Injury Rates in Elite Distance Athletes. Int. J. Sport Nutr. Exerc. Metab. 2018, 28,
403–411. [CrossRef]
112. Areta, J.L.; Taylor, H.L.; Koehler, K. Low energy availability: History, definition and evidence of its endocrine, metabolic and
physiological effects in prospective studies in females and males. Graefes Arch. Clin. Exp. Ophthalmol. 2021, 121, 1–21. [CrossRef]
113. Tenforde, A.S.; Carlson, J.L.; Chang, A.; Sainani, K.L.; Shultz, R.; Kim, J.H.; Cutti, P.; Golden, N.H.; Fredericson, M. Association of
the Female Athlete Triad Risk Assessment Stratification to the Development of Bone Stress Injuries in Collegiate Athletes. Am. J.
Sports Med. 2017, 45, 302–310. [CrossRef]
114. Loucks, A.B.; Kiens, B.; Wright, H.H. Energy availability in athletes. J. Sports Sci. 2011, 29 (Suppl. 1), S7–S15. [CrossRef] [PubMed]
115. Ihle, R.; Loucks, A.B. Dose-Response Relationships Between Energy Availability and Bone Turnover in Young Exercising Women.
J. Bone Miner. Res. 2004, 19, 1231–1240. [CrossRef]
116. Sawyer, J.C.; Wood, R.J.; Davidson, P.W.; Collins, S.M.; Matthews, T.D.; Gregory, S.M.; Paolone, V.J. Effects of a Short-Term
Carbohydrate-Restricted Diet on Strength and Power Performance. J. Strength Cond. Res. 2013, 27, 2255–2262. [CrossRef]
[PubMed]
117. Hammond, K.M.; Sale, C.; Fraser, W.; Tang, J.; Shepherd, S.O.; Strauss, J.A.; Close, G.L.; Cocks, M.; Louis, J.; Pugh, J.; et al.
Post-exercise carbohydrate and energy availability induce independent effects on skeletal muscle cell signalling and bone
turnover: Implications for training adaptation. J. Physiol. 2019, 597, 4779–4796. [CrossRef]
118. Morton, R.W.; Murphy, K.T.; McKellar, S.R.; Schoenfeld, B.J.; Henselmans, M.; Helms, E.; Aragon, A.A.; Devries, M.C.; Banfield, L.;
Krieger, J.W.; et al. A systematic review, meta-analysis and meta-regression of the effect of protein supplementation on resistance
training-induced gains in muscle mass and strength in healthy adults. Br. J. Sports Med. 2018, 52, 376–384. [CrossRef]
119. Barzel, U.S.; Massey, L.K. Excess Dietary Protein Can Adversely Affect Bone. J. Nutr. 1998, 128, 1051–1053. [CrossRef] [PubMed]
120. Shams-White, M.M.; Chung, M.; Du, M.; Fu, Z.; Insogna, K.L.; Karlsen, M.C.; LeBoff, M.S.; A Shapses, S.; Sackey, J.; Wallace, T.C.;
et al. Dietary protein and bone health: A systematic review and meta-analysis from the National Osteoporosis Foundation. Am. J.
Clin. Nutr. 2017, 105, ajcn145110. [CrossRef] [PubMed]
Nutrients 2022, 14, 53 18 of 20

121. Shams-White, M.M.; Chung, M.; Fu, Z.; Insogna, K.L.; Karlsen, M.C.; LeBoff, M.S.; Shapses, S.A.; Sackey, J.; Shi, J.;
Wallace, T.C.; et al. Animal versus plant protein and adult bone health: A systematic review and meta-analysis from the National
Osteoporosis Foundation. PLoS ONE 2018, 13, e0192459. [CrossRef]
122. Babraj, J.; Smith, K.; Cuthbertson, D.J.; Rickhuss, P.; Dorling, J.S.; Rennie, M.J. Human Bone Collagen Synthesis Is a Rapid,
Nutritionally Modulated Process. J. Bone Miner. Res. 2005, 20, 930–937. [CrossRef] [PubMed]
123. Delmi, M.; Rapin, C.-H.; Bengoa, J.-M.; Bonjour, J.-P.; Vasey, H.; Delmas, P. Dietary supplementation in elderly patients with
fractured neck of the femur. Lancet 1990, 335, 1013–1016. [CrossRef]
124. Schurch, M.-A.; Rizzoli, R.; Slosman, D.; Vadas, L.; Vergnaud, P.; Bonjour, J.-P. Protein Supplements Increase Serum Insulin-
Like Growth Factor-I Levels and Attenuate Proximal Femur Bone Loss in Patients with Recent Hip Fracture: A randomized,
double-blind, placebo-controlled trial. Ann. Intern. Med. 1998, 128, 801–809. [CrossRef]
125. Lust, C.A.; Mountjoy, M.; Robinson, L.E.; Oliver, J.M.; Ma, D.W. Sports-related concussions and subconcussive impacts in athletes:
Incidence, diagnosis, and the emerging role of EPA and DHA. Appl. Physiol. Nutr. Metab. 2020, 45, 886–892. [CrossRef]
126. Zuckerman, S.L.; Kerr, Z.Y.; Yengo-Kahn, A.; Wasserman, E.; Covassin, T.; Solomon, G.S. Epidemiology of Sports-Related
Concussion in NCAA Athletes From 2009-2010 to 2013-2014: Incidence, Recurrence, and Mechanisms. Am. J. Sports Med. 2015, 43,
2654–2662. [CrossRef] [PubMed]
127. Pierpoint, L.A.; Collins, C. Epidemiology of Sport-Related Concussion. Clin. Sports Med. 2021, 40, 1–18. [CrossRef] [PubMed]
128. Harmon, K.G.; Drezner, J.; Gammons, M.; Guskiewicz, K.; Halstead, M.; Herring, S.; Kutcher, J.; Pana, A.; Putukian, M.;
Roberts, W. American Medical Society for Sports Medicine position statement: Concussion in sport. Br. J. Sports Med. 2012, 47,
15–26. [CrossRef]
129. Trojian, T.H.; Wang, D.H.; Leddy, J.J. Nutritional Supplements for the Treatment and Prevention of Sports-Related Concussion—
Evidence Still Lacking. Curr. Sports Med. Rep. 2017, 16, 247–255. [CrossRef] [PubMed]
130. Barrett, E.C.; McBurney, M.I.; Ciappio, E.D. ω-3 Fatty Acid Supplementation as a Potential Therapeutic Aid for the Recovery
from Mild Traumatic Brain Injury/Concussion1,2. Adv. Nutr. 2014, 5, 268–277. [CrossRef]
131. Wu, A.; Ying, Z.; Gomez-Pinilla, F. Dietary curcumin counteracts the outcome of traumatic brain injury on oxidative stress,
synaptic plasticity, and cognition. Exp. Neurol. 2006, 197, 309–317. [CrossRef]
132. Mills, J.D.; Hadley, K.; Bailes, J.E. Dietary Supplementation with the Omega-3 Fatty Acid Docosahexaenoic Acid in Traumatic
Brain Injury. Neurosurgery 2011, 68, 474–481. [CrossRef] [PubMed]
133. Wu, A.; Ying, Z.; Gomez-Pinilla, F. The Salutary Effects of DHA Dietary Supplementation on Cognition, Neuroplasticity, and
Membrane Homeostasis after Brain Trauma. J. Neurotrauma 2011, 28, 2113–2122. [CrossRef] [PubMed]
134. Wu, A.; Ying, Z.; Gomez-Pinilla, F. Dietary strategy to repair plasma membrane after brain trauma: Implications for plasticity and
cognition. Neurorehabil. Neural Repair 2014, 28, 75–84. [CrossRef] [PubMed]
135. Hedström, M.; Ljungqvist, O.; Cederholm, T. Metabolism and catabolism in hip fracture patients: Nutritional and anabolic
intervention—A review. Acta Orthop. 2006, 77, 741–747. [CrossRef] [PubMed]
136. Weissman, C. The metabolic response to stress: An overview and update. Anesthesiology 1990, 73, 308–327. [CrossRef]
137. Bannister, W.K.; Sattilaro, A.J. Vomiting and aspiration during anesthesia. J. Am. Soc. Anesthesiol. 1962, 23, 251–264. [CrossRef]
138. Jones, C.; Badger, S.A.; Hannon, R. The role of carbohydrate drinks in pre-operative nutrition for elective colorectal surgery. Ann.
R. Coll. Surg. Engl. 2011, 93, 504–507. [CrossRef]
139. Nygren, J.; Thorell, A.; Ljungqvist, O. Preoperative oral carbohydrate nutrition: An update. Curr. Opin. Clin. Nutr. Metab. Care
2001, 4, 255–259. [CrossRef] [PubMed]
140. Magne, H.; Savary-Auzeloux, I.; Rémond, D.; Dardevet, D. Nutritional strategies to counteract muscle atrophy caused by disuse
and to improve recovery. Nutr. Res. Rev. 2013, 26, 149–165. [CrossRef]
141. Wall, B.T.; Dirks, M.; Snijders, T.; Senden, J.M.G.; Dolmans, J.; Van Loon, L.J.C. Substantial skeletal muscle loss occurs during only
5 days of disuse. Acta Physiol. 2013, 210, 600–611. [CrossRef]
142. Jones, S.W.; Hill, R.J.; Krasney, P.A.; O’Conner, B.; Peirce, N.; Greenhaff, P. Disuse atrophy and exercise rehabilitation in humans
profoundly affects the expression of genes associated with the regulation of skeletal muscle mass. FASEB J. 2004, 18, 1025–1027.
[CrossRef] [PubMed]
143. Paddon-Jones, D.; Sheffield-Moore, M.; Urban, R.J.; Sanford, A.P.; Aarsland, A.; Wolfe, R.R.; Ferrando, A.A. Essential Amino Acid
and Carbohydrate Supplementation Ameliorates Muscle Protein Loss in Humans during 28 Days Bedrest. J. Clin. Endocrinol.
Metab. 2004, 89, 4351–4358. [CrossRef] [PubMed]
144. Kouw, I.W.; Groen, B.B.; Smeets, J.; Kramer, I.F.; van Kranenburg, J.M.; Nilwik, R.; Geurts, J.A.; Broeke, R.H.T.; Poeze, M.; van
Loon, L.J.; et al. One Week of Hospitalization Following Elective Hip Surgery Induces Substantial Muscle Atrophy in Older
Patients. J. Am. Med. Dir. Assoc. 2019, 20, 35–42. [CrossRef] [PubMed]
145. Dreyer, H.C.; Drummond, M.J.; Pennings, B.; Fujita, S.; Glynn, E.L.; Chinkes, D.L.; Dhanani, S.; Volpi, E.; Rasmussen, B.B.
Leucine-enriched essential amino acid and carbohydrate ingestion following resistance exercise enhances mTOR signaling and
protein synthesis in human muscle. Am. J. Physiol. Metab. 2008, 294, E392–E400. [CrossRef] [PubMed]
146. Demling, R.H. Nutrition, Anabolism, and the Wound Healing Process: An Overview. Eplasty 2009, 9, e9. [PubMed]
147. Cockburn, E.; Stevenson, E.; Hayes, P.R.; Robson-Ansley, P.; Howatson, G. Effect of milk-based carbohydrate-protein supplement
timing on the attenuation of exercise-induced muscle damage. Appl. Physiol. Nutr. Metab. 2010, 35, 270–277. [CrossRef]
Nutrients 2022, 14, 53 19 of 20

148. Nosaka, K.; Sacco, P.; Mawatari, K. Effects of Amino Acid Supplementation on Muscle Soreness and Damage. Int. J. Sport Nutr.
Exerc. Metab. 2006, 16, 620–635. [CrossRef]
149. Wojcik, J.R.; Walber-Rankin, J.; Smith, L.L.; Gwazdauskas, F.; Walberg-Rankin, J. Comparison of Carbohydrate and Milk-Based
Beverages on Muscle Damage and Glycogen Following Exercise. Int. J. Sport Nutr. Exerc. Metab. 2001, 11, 406–419. [CrossRef]
150. Blacker, S.D.; Williams, N.C.; Fallowfield, J.L.; Bilzon, J.L.; Willems, M.E. Carbohydrate vs protein supplementation for recovery
of neuromuscular function following prolonged load carriage. J. Int. Soc. Sports Nutr. 2010, 7, 2. [CrossRef]
151. Pasiakos, S.; Lieberman, H.R.; McLellan, T.M. Effects of Protein Supplements on Muscle Damage, Soreness and Recovery of
Muscle Function and Physical Performance: A Systematic Review. Sports Med. 2014, 44, 655–670. [CrossRef]
152. Milsom, J.; Barreira, P.; Burgess, D.J.; Iqbal, Z.; Morton, J.P.; Barreria, P. Case Study: Muscle Atrophy and Hypertrophy in a Premier
League Soccer Player During Rehabilitation from ACL Injury. Int. J. Sport Nutr. Exerc. Metab. 2014, 24, 543–552. [CrossRef]
[PubMed]
153. Owens, D.J.; Twist, C.; Cobley, J.N.; Howatson, G.; Close, G.L. Exercise-induced muscle damage: What is it, what causes it and
what are the nutritional solutions? Eur. J. Sport Sci. 2019, 19, 71–85. [CrossRef]
154. Cobley, J.N.; McHardy, H.; Morton, J.P.; Nikolaidis, M.G.; Close, G. Influence of vitamin C and vitamin E on redox signaling:
Implications for exercise adaptations. Free Radic. Biol. Med. 2015, 84, 65–76. [CrossRef]
155. Vieira, C.P.; Guerra, F.D.R.; De Oliveira, L.P.; Almeida, M.; Marcondes, M.C.C.; Pimentell, E.R. Green tea and glycine aid in the
recovery of tendinitis of the Achilles tendon of rats. Connect. Tissue Res. 2015, 56, 50–58. [CrossRef]
156. Vieira, C.P.; De Oliveira, L.P.; Guerra, F.D.R.; Almeida, M.D.S.D.; Marcondes, M.C.C.G.; Pimentel, E.R. Glycine Improves
Biochemical and Biomechanical Properties Following Inflammation of the Achilles Tendon. Anat. Rec. Adv. Integr. Anat. Evol. Biol.
2015, 298, 538–545. [CrossRef] [PubMed]
157. Buchman, A.; O’Brien, W.; Ou, C.; Rognerud, C.; Alvarez, M.; Dennis, K.; Ahn, C. The Effect of Arginine or Glycine Supplementa-
tion on Gastrointestinal Function, Muscle Injury, Serum Amino Acid Concentrations and Performance During a Marathon Run.
Int. J. Sports Med. 1999, 20, 315–321. [CrossRef]
158. Wolfe, R.R. Branched-chain amino acids and muscle protein synthesis in humans: Myth or reality? J. Int. Soc. Sports Nutr. 2017,
14, 30. [CrossRef] [PubMed]
159. Blomstrand, E.; Eliasson, J.; Karlsson, H.; Köhnke, R. Branched-Chain Amino Acids Activate Key Enzymes in Protein Synthesis
after Physical Exercise. J. Nutr. 2006, 136 (Suppl. 1), 269S–273S. [CrossRef] [PubMed]
160. Volpi, E.; Kobayashi, H.; Sheffield-Moore, M.; Mittendorfer, B.; Wolfe, R.R. Essential amino acids are primarily responsible for the
amino acid stimulation of muscle protein anabolism in healthy elderly adults. Am. J. Clin. Nutr. 2003, 78, 250–258. [CrossRef]
161. Katsanos, C.S.; Kobayashi, H.; Sheffield-Moore, M.; Aarsland, A.; Wolfe, R.R. A high proportion of leucine is required for optimal
stimulation of the rate of muscle protein synthesis by essential amino acids in the elderly. Am. J. Physiol. Metab. 2006, 291,
E381–E387. [CrossRef]
162. O’Brien, C.P. Alcohol and sport. Impact of social drinking on recreational and competitive sports performance. Sports Med. 1993,
15, 71–77.
163. Martens, M.P.; Dams-O’Connor, K.; Beck, N.C. A systematic review of college student-athlete drinking: Prevalence rates,
sport-related factors, and interventions. J. Subst. Abus. Treat. 2006, 31, 305–316. [CrossRef] [PubMed]
164. Watten, R.G. Sports, physical exercise and use of alcohol. Scand. J. Med. Sci. Sports 2007, 5, 364–368. [CrossRef] [PubMed]
165. Windle, M.; Barnes, G.M. Similarities and Differences in Correlates of Alcohol Consumption and Problem Behaviors Among
Male and Female Adolescents. Int. J. Addict. 1988, 23, 707–728. [CrossRef] [PubMed]
166. Jung, M.K.; Callaci, J.J.; Lauing, K.L.; Otis, J.S.; Radek, K.A.; Jones, M.K.; Kovacs, E.J. Alcohol Exposure and Mechanisms of Tissue
Injury and Repair. Alcohol. Clin. Exp. Res. 2011, 35, 392–399. [CrossRef]
167. Barnes, M.J. Alcohol: Impact on Sports Performance and Recovery in Male Athletes. Sports Med. 2014, 44, 909–919. [CrossRef]
[PubMed]
168. Parr, E.; Camera, D.; Areta, J.; Burke, L.M.; Phillips, S.; Hawley, J.A.; Coffey, V.G. Alcohol Ingestion Impairs Maximal Post-Exercise
Rates of Myofibrillar Protein Synthesis following a Single Bout of Concurrent Training. PLoS ONE 2014, 9, e88384. [CrossRef]
169. Lang, C.H.; Frost, R.A.; Deshpande, N.; Kumar, V.; Vary, T.C.; Jefferson, L.S.; Kimball, S.R. Alcohol impairs leucine-mediated
phosphorylation of 4E-BP1, S6K1, eIF4G, and mTOR in skeletal muscle. Am. J. Physiol. Metab. 2003, 285, E1205–E1215. [CrossRef]
[PubMed]
170. Lang, C.H.; A Frost, R.; Kumar, V.; Wu, D.; Vary, T.C. Impaired protein synthesis induced by acute alcohol intoxication is
associated with changes in eIF4E in muscle and eIF2B in liver. Alcohol. Clin. Exp. Res. 2000, 24, 322–331. [CrossRef]
171. Vargas, R.; Lang, C.H. Alcohol Accelerates Loss of Muscle and Impairs Recovery of Muscle Mass Resulting from Disuse Atrophy.
Alcohol. Clin. Exp. Res. 2008, 32, 128–137. [CrossRef] [PubMed]
172. Jänicke-Lorenz, J.; Lorenz, R. Alcoholism and fracture healing. Arch. Orthop. Trauma. Surg. 1984, 103, 286–289. [CrossRef]
[PubMed]
173. Messingham, K.A.; Faunce, D.E.; Kovacs, E.J. Alcohol, injury, and cellular immunity. Alcohol 2002, 28, 137–149. [CrossRef]
174. Maughan, R.J. Alcohol and football. J. Sports Sci. 2006, 24, 741–748. [CrossRef] [PubMed]
175. Stokes, K.A.; Jones, B.; Bennett, M.; Close, G.L.; Gill, N.; Hull, J.H.; Kasper, A.M.; Kemp, S.P.; Mellalieu, S.D.; Peirce, N.; et al.
Returning to Play after Prolonged Training Restrictions in Professional Collision Sports. Endoscopy 2020, 41, 895–911. [CrossRef]
[PubMed]
Nutrients 2022, 14, 53 20 of 20

176. Impey, S.G.; Hearris, M.A.; Hammond, K.M.; Bartlett, J.D.; Louis, J.; Close, G.; Morton, J.P. Fuel for the Work Required: A
Theoretical Framework for Carbohydrate Periodization and the Glycogen Threshold Hypothesis. Sports Med. 2018, 48, 1031–1048.
[CrossRef] [PubMed]
177. Frankenfield, D. Energy Expenditure and Protein Requirements After Traumatic Injury. Nutr. Clin. Pr. 2006, 21, 430–437.
[CrossRef] [PubMed]
178. Tipton, K.D. Dietary strategies to attenuate muscle loss during recovery from injury. Nestle Nutr. Inst. Workshop Ser. 2013, 75,
51–61.
179. Waters, R.L.; Campbell, J.; Perry, J. Energy Cost of Three-Point Crutch Ambulation in Fracture Patients. J. Orthop. Trauma 1987, 1,
170–173. [CrossRef]
180. Layman, D.K. Dietary Guidelines should reflect new understandings about adult protein needs. Nutr. Metab. 2009, 6, 12.
[CrossRef] [PubMed]
181. Layman, D.K.; Boileau, R.A.; Erickson, D.J.; Painter, J.E.; Shiue, H.; Sather, C.; Christou, D.D. A Reduced Ratio of Dietary
Carbohydrate to Protein Improves Body Composition and Blood Lipid Profiles during Weight Loss in Adult Women. J. Nutr.
2003, 133, 411–417. [CrossRef] [PubMed]
182. Weigle, D.S.; Breen, P.A.; Matthys, C.C.; Callahan, H.S.; Meeuws, K.E.; Burden, V.R.; Purnell, J.Q. A high-protein diet induces
sustained reductions in appetite, ad libitum caloric intake, and body weight despite compensatory changes in diurnal plasma
leptin and ghrelin concentrations. Am. J. Clin. Nutr. 2005, 82, 41–48. [CrossRef] [PubMed]

You might also like