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ORIGINAL RESEARCH article

Front. Sports Act. Living, 06 April 2023
Sec. Sport and Exercise Nutrition
This article is part of the Research Topic Women in Sport and Exercise Nutrition: 2022 View all 4 articles

Micronutrient supplement intakes among collegiate and masters athletes: A cross-sectional study

  • 1Department of Human Nutrition, Foods, and Exercise, Virginia Polytechnic Institute and State University (Virginia Tech), Blacksburg, VA, United States
  • 2Nutrition & Scientific Affairs, Worldwide Sport Nutritional Supplements, Bohemia, NY, United States

Objective: In our cross-sectional study, we evaluated micronutrient supplementation intake among Collegiate and Masters Athletes.

Methods: We conducted a cross-sectional study to assess micronutrient supplementation consumption in Collegiate and Masters Athletes, comparing sex and sport classification within each respective group. Micronutrient supplement consumption data were measured using a Food Frequency Questionnaire. A two-way analysis of variance was used to explore the differences among Collegiate and Masters Athletes' supplement intakes of the following vitamins and minerals: vitamins A, B6, B12, C, E, D, and calcium, folate, iron, magnesium niacin, riboflavin, selenium, thiamine, and zinc. When significant differences were found, a Bonferroni post hoc test was performed to identify specific group differences. The significance level was set a priori at p < 0.05.

Results: A total of 198 athletes (105 females and 93 males) were included in the study. Participants were 36.16 ± 12.33 years of age. Collegiate male athletes had significantly greater vitamin A [1,090.51 ± 154.72 vs. 473.93 ± 233.18 mg retinol activity equivalents (RAE)/day] (p < 0.036), folate [337.14 ± 44.79 vs. 148.67 ± 67.50 mcg dietary folate equivalents (DFE)/day] (p < 0.027), and magnesium (65.35 ± 8.28 vs. 31.28 ± 12.48 mg/day) (p < 0.031) intakes compared to Collegiate female athletes. Collegiate CrossFit Athletes (940.71 ± 157.54 mg/day) had a significantly greater vitamin C intake compared to Collegiate General Athletes (156.34 ± 67.79 mg/day) (p < 0.005), Collegiate Triathletes (88.57 ± 148.53 mg/day) (p < 0.027), Collegiate Resistance Training Athletes (74.28 ± 143.81 mg/day) (p < 0.020), and Collegiate Powerlifters (175.71 ± 128.63 mg/day) (p < 0.044). Masters females had significantly greater calcium intakes compared to Masters males (494.09 ± 65.73 vs.187.89 ± 77.23 mg/day, respectively) (p < 0.002). Collegiate Runners (41.35 ± 6.53 mg/day) had a significantly greater iron intake compared to Collegiate Powerlifters (4.50 ± 6.53 mg/day) (p < 0.024). Masters Swimmers (61.43 ± 12.10 mg/day) had significantly greater iron intakes compared to Masters General Athletes (13.97 ± 3.56 mg/day) (p < 0.014), Masters Runners (17.74 ± 2.32 mg/day) (p < 0.03), Masters Triathletes (11.95 ± 3.73 mg/day) (p < 0.008), Masters CrossFit Athletes (15.93 ± 5.36 mg/day) (p < 0.043), Masters Rowers (9.10 ± 3.36 mg/day) (p < 0.003), and Masters Cyclists (1.71 ± 9.88 mg/day) (p < 0.011). Masters Powerlifters (47.14 ± 9.65 mg/day) had significantly greater zinc intakes compared to Masters General Athletes (9.57 ± 2.84 mg/day) (p < 0.015), Masters Runners (10.67 ± 1.85 mg/day) (p < 0.017), Masters Triathletes (10.24 ± 2.98 mg/day) (p < 0.020), Masters Rowers (9.33 ± 2.68 mg/day) (p < 0.013), and Masters Cyclists (1.43 ± 7.88 mg/day) (p < 0.019). There were no other significant differences among the other micronutrient supplement intakes between the sexes or among the sport classification.

Conclusion: We reported significant differences among female and male Collegiate and Masters Athletes. Additionally, we reported significant differences among Collegiate and Masters Athletes sport classifications. Further research should examine both dietary and micronutrient supplement intake among Collegiate and Masters Athletes to examine the extent that athletes exceed the Recommended Dietary Allowances (RDA), and the potential effects on health and performance.

1. Introduction

Micronutrients play a vital role in the maintenance of tissue function and are required for a number of metabolic reactions, including energy production. During physical activity, micronutrients are involved in roles such as muscle contraction, oxygen transport, and the metabolism of carbohydrates, protein and fat (13). Physical activity increases the utilization of micronutrients by increasing energy metabolism production, increased demand from exercising tissue, and losses from sweat, urine, and feces (2, 4, 5). Physical activity, coupled with insufficient energy intake, may lead to vitamin and mineral deficiencies (3), which can lead to impaired athletic performance and health. Athletes may take a vitamin and mineral supplement, or take individual vitamins and minerals based on the potential performance benefit of the supplement (6). Further, athletes may take micronutrient supplements as a result of inadequate dietary intake, dietary restrictions, or consuming vegan/vegetarian diets (7, 8). A Joint Position Stand published by the American College of Sports Medicine, the Academy of Nutrition and Dietetics, and the Dietitians of Canada (3) concluded that micronutrient supplementation may be required if athletes restrict their energy intake, remove food groups from their diets, or consume high carbohydrate diets, and/or low micronutrient density diets. Endurance athletes such as runners, cyclists, and triathletes may be most at risk for micronutrient deficiency because of low energy consumption, coupled with longer physical activity duration and increased sweat rate (9, 10). Wirnitzer et al. (11) reported that 51% of endurance runners regularly consumed a vitamin and mineral supplement.

Previous researchers have reported that 80% of collegiate athletes use supplements, one of the most common being multi-vitamin and multi-mineral supplements (6, 1214). Parnell et al. (15) reported that college-age athletes (19–25 years of age) who took individual vitamin, mineral or multi-vitamin/multi-mineral supplements thought their athletic performance would improve (15).

Masters Athletes are usually between 35 and 50 years of age and compete in organized sports (16, 17); however, they can be younger than 35 years of age depending on the specific sport's requirement (17). Masters Athletes may be more likely to take micronutrient supplements because of the various challenges that occur with aging and recovery (1820).

The prevalence of supplement use among female athletes is similar to male athletes, although their reasons for use differ (6, 13, 21, 22). Bailey et al. (21) reported that supplement use among 2,066 females, ≥20 years of age, was mainly to improve bone health and to increase energy. Similarly, Barrack et al. (22) reported that, among 557 Collegiate Athletes (259 females, 298 males), the use of a micronutrient supplement was highest among female athletes wanting to improve health. Senekal et al. (23) reported that, regardless of age, younger men (21–30 years of age) and older males (≥45 years of age) took micronutrient supplements for performance improvements and to maintain overall health.

Micronutrient supplementation has had widespread use, regardless of age, sex and sport level (6, 13, 23, 24, 25). The purpose of our study was to compare the differences in vitamin and mineral supplementation between the sexes and among various sport classifications in Collegiate Athletes and Masters Athletes.

2. Materials and methods

2.1. Study design and participants

We conducted a cross-sectional study that included Collegiate and Masters Athletes from multiple sporting backgrounds. Participant eligibility was assessed using an online survey. Participants qualified based on the following inclusion criteria: non-smokers, Collegiate or Masters Athletes who exercised at least two days per week. Exclusion criteria included: sedentary individuals (defined as persons who exercised less than two days a week), individuals diagnosed with chronic disease (e.g., cardiovascular disease, hypertension) without written permission from their physician, individuals taking medications without written permission from their physician, adults unable to consent, individuals less than 18 years of age, and pregnant. Although Masters Athletes' age can vary among different sports, we defined Masters Athletes as being 26 years of age and older, based on the fact that some sports consider ≥21 years of age as a Masters Athlete, while others consider ≥35 years of age as a Masters Athlete. The sport classifications used in our study were General Athletes, Runners, Triathletes, Rowers, Cyclists, CrossFit Athletes, Resistance Training Athletes, Powerlifters, Soccer Athletes, Track Athletes, Tennis Athletes, Football Athletes, Ice Hockey Athletes, Field Hockey Athletes, and Swimmers. General Athletes were defined as athletes who engaged in multiple sports. Athlete levels were characterized as recreational, club, varsity (applies only to Collegiate Athletes) and professional (one Masters Triathlete). The requirements previously mentioned to classify each athlete aligns with the Tier 1 and 2 criteria for participation classification established by McKay et al. (26). Each potential participant was asked to complete an online survey via the REDCap™ software. Drexel University's Institutional Review Board approved all study procedures and protocols prior to any data collection.

2.2. Measurements

Participants who qualified were scheduled to have their measurements taken at the Nutrition Sciences Laboratory at Drexel University. Body weight and height were measured twice on a calibrated scale and stadiometer, respectively. Body weight and height were measured twice to ensure accuracy. Waist circumference was measured one inch above the umbilicus, three times to ensure accuracy, using a soft measuring tape. Afterwards, the participants completed the Block 2005 Food Frequency Questionnaire (FFQ). The Block 2005 FFQ is a self-administered FFQ that took about 30–40 min to complete. The Block 2005 FFQ questions about supplements are limited only to single vitamin, mineral, and multivitamin and multimineral use. Additionally, there were no questions about supplements that contained vitamins and minerals such as protein powders, sport gels/powders, pre-workout supplements, and fruit and vegetable powders. The micronutrient supplementation in which we focused for this study were: vitamins A, B6, B12, C, E, D, and calcium, folate, iron, magnesium niacin, riboflavin, selenium, thiamine, and zinc. The Block FFQs were sent to NutritionQuest (Berkeley, CA) for analyses.

2.3. Statistical analyses

Statistical analyses were performed using using SPSS Statistics (Version 26.0. Armonk, NY, IBM Corp). A two-way analysis of variance (ANOVA) was used to compare the following vitamin and mineral supplement intakes: vitamins A, B6, B12, C, E, D, and calcium, folate, iron, magnesium niacin, riboflavin, selenium, thiamine, and zinc among Collegiate and Masters Athlete sex and sport classifications. When significant differences were found, a Bonferroni post hoc test was performed to identify specific group differences between sex and among sport classifications among Collegiate and Masters athletes. The significance level was set a priori at p < 0.05, no additional corrections were conducted for type II errors. The descriptive characteristics of Collegiate and Masters Athletes groups and subgroups was reported as mean ± standard deviation (SD). Due to uneven numbers of participants among sport classifications, vitamin and mineral intake were reported as estimated marginal means ± standard error (SE). Normality of the data was evaluated with visual inspections of histograms and normal probability plots and the Kruskal–Wallis test.

3. Results

3.1. Descriptive statistics

Our study included 365 adults, 18 years of age or older, who were Collegiate and Masters Athletes. A total of 198 athletes (105 females and 93 males) who used at least one micronutrient supplement were included in the final statistical analyses. Table 1 outlines the descriptive characteristics of the 198 athletes who submitted complete data regarding micronutrient supplement use.

TABLE 1
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Table 1. Descriptive characteristics of collegiate and masters athletes.

3.2. Micronutrient supplement use

There were significant differences in supplement use among Collegiate female and male athletes (Table 2). Collegiate male athletes had significantly greater vitamin A [1,090.51 ± 154.72 vs. 473.93 ± 233.18 mg retinol activity equivalents (RAE)/day] (p < 0.036), folate [337.14 ± 44.79 vs. 148.67 ± 67.50 mcg dietary folate equivalents (DFE)/day] (p < 0.027), and magnesium (65.35 ± 8.28 vs. 31.28 ± 12.48 mg/day) (p < 0.031) intakes compared to Collegiate female athletes, respectively. There were significant differences among sport classification supplement use (Table 3) among Collegiate Athletes. Collegiate CrossFit Athletes (940.71 ± 157.54 mg/day) had a significantly greater vitamin C intake compared to Collegiate General Athletes (156.34 ± 67.79 mg/day) (p < 0.005), Collegiate Triathletes (88.57 ± 148.53 mg/day) (p < 0.027), Collegiate Resistance Training Athletes (74.28 ± 143.81 mg/day) (p < 0.020), and Collegiate Powerlifters (175.71 ± 128.63 mg/day) (p < 0.044). Collegiate Runners (41.35 ± 6.53 mg/day) had a significantly greater iron intake compared to Collegiate Powerlifters (4.50 ± 6.53 mg/day) (p < 0.024). There were significant differences among Masters female and male athletes' supplement use (Table 4). Masters female athletes had significantly greater calcium intakes compared to Masters male athletes (494.09 ± 65.73 vs.187.89 ± 77.23 mg/day, respectively) (p < 0.002). There were also significant differences in supplement use based on sport classification among Masters Athletes (Table 5). Masters Swimmers (61.43 ± 12.10 mg/day) had significantly greater iron intakes compared to Masters General Athletes (13.97 ± 3.56 mg/day) (p < 0.014), Masters Runners (17.74 ± 2.32 mg/day) (p < 0.03), Masters Triathletes (11.95 ± 3.73 mg/day)(p < 0.008), Masters CrossFit Athletes (15.93 ± 5.36 mg/day) (p < 0.043), Masters Rowers (9.10 ± 3.36 mg/day) (p < 0.003), and Masters Cyclists (1.71 ± 9.88 mg/day) (p < 0.011). Masters Powerlifters (47.14 ± 9.65 mg/day) had significantly greater zinc intakes compared to Masters General Athletes (9.57 ± 2.84 mg/day) (p < 0.015), Masters Runners (10.67 ± 1.85 mg/day) (p < 0.017), Masters Triathletes (10.24 ± 2.98 mg/day) (p < 0.020), Masters Rowers (9.33 ± 2.68 mg/day) (p < 0.013), and Masters Cyclists (1.43 ± 7.88 mg/day) (p < 0.019) (Table 5). There were no other significant differences between the Collegiate and Masters groups.

TABLE 2
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Table 2. Micronutrient supplementation among female and male collegiate athletes.

TABLE 3
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Table 3. Collegiate athletes sports classification micronutrient supplementation.

TABLE 4
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Table 4. Micronutrient supplementation among female and male masters athletes.

TABLE 5
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Table 5. Masters athletes sport classification micronutrient supplementation.

4. Discussion

The purpose of this study was to investigate supplement intake among Collegiate and Masters Athletes in various sport groups. As well as, examine sex differences in supplement intake among Collegiate Athletes and Masters Athletes. Our study is one of the first to compare micronutrient supplement intake among sex and multiple sport classifications in Collegiate and Masters Athletes, and also adds to the limited body of evidence on supplement use in Masters Athletes.

4.1. Collegiate athletes

When comparing sex, we reported that Collegiate male athletes had significantly greater vitamin A supplement intakes compared to Collegiate female athletes. The reported vitamin A supplement intakes in our study were higher than athletes of the same age in other studies (27, 28) Patlar et al. (27) supplemented 10 males, 22.85 ± 0.26 years of age, with 300 mg/day of vitamin A for four weeks. The participants completed a Bruce protocol test each week for four weeks. The authors (27) reported that vitamin A supplementation did not reduce lipid peroxidation and muscle damage post-exercise. Teixeira et al. (28) randomized 20 kayakers (6 females and 14 males), 19.1 ± 3.8 years of age (supplement group) and 20.3 ± 3.3 years of age (placebo group). The supplement group was given an antioxidant containing 272 mg of alpha-tochoperol, 400 mg of vitamin C, 30 mg of β-carotene, 2 mg of lutein, 400 mcg of selenium, 30 mg of zinc, and 600 mg of magnesium for four weeks. The athletes completed two 1,000-m flat water time trials in the four-week period. The authors (28) reported no significant differences in race time between either group pre- or post-supplementation. Lastly, since β-carotene was combined with other micronutrients, it is difficult to determine the direct effect of β-carotene. There is a lack of studies reporting the benefit of vitamin A or β-carotene on exercise performance (2932). In their supplement consensus statements, neither the IOC or the International Society of Sports Nutrition (ISSN) list vitamin A as providing any performance benefit (30, 31).

Folate is a B vitamin responsible for red blood cell formation and amino acid metabolism. In our study, Collegiate female athletes' supplementation for folate (148.67 ± 67.50 mcg DFE/day) were lower than those reported by female athletes in previous studies (33, 34). Woolf et al. (33) reported higher folate supplementation among 58 highly active (564 ± 272 mcg DFE/day) and sedentary females (935 ± 438 mcg DFE/day) compared to our population. Bailey et al. (34) reported that folate intakes for females, 19 to 30 years of age, was 615 ± 17 mcg DFE/day, although they combined dietary and supplemental folate. Further, while most of the literature focuses on dietary intake of folate, there is limited evidence of folate supplementation intake among Collegiate female athletes. Inadequate folate intake for women puts them at risk for anemia, which may also affect their physical performance (4, 35).

We reported that Collegiate male athletes had significantly greater magnesium supplement intakes compared to Collegiate female athletes (Table 2). The reported intake of magnesium supplementation in our study was lower than athletes of the same age in other studies (36, 37). In a randomized control trial, Kass et al. (36) supplemented 16 male athletes, 20.88 ± 1.82 years of age, who had dietary magnesium intakes above and below the United Kingdom Reference Nutrient Intake (RNI) of 300 mg/day for adult males. The supplement group took 300 mg/day of magnesium oxide for two weeks. Participants in the placebo group did not receive supplementation. A maximal aerobic capacity cycle test was performed for 30 min, followed by three, five-second maximal isometric bench presses. The authors (36) reported no significant differences in aerobic and resistance performance between the supplement and placebo groups.

Cordova et al. (37) randomized 18 male cyclists, 26.2 ± 1.81 years of age, into magnesium-supplemented and control groups. The magnesium-supplemented group was given 400 mg/day (magnesium 400 supra Kapsel®, Sanct Bernhard, Barcelona, Spain), the control group did not receive a supplement. The aim was to examine the effect of magnesium supplementation in reducing muscle damage during a 21-day stage cycling race (“Vuelta a España”, which is about 3,300 km). The authors (37) reported no differences in performance between both groups.

While magnesium supplementation does not affect athletic performance (30, 31, 36, 37), it may be prudent for athletes to supplement in addition to their dietary intake to meet their respective Recommended Dietary Allowances (RDA). Volpe (38) stated that the majority of athletes are not meeting the RDA for magnesium. Further, Hunt et al. (39) reported that, although there is a high rate of magnesium supplement use among athletes, magnesium intakes are still inadequate to meet the average requirement.

We reported higher vitamin C supplementation in Collegiate CrossFit Athletes compared to other athletes; however, there is a lack of research on supplement in CrossFit Athletes (40, 41). Although, we reported similar vitamin C supplement intakes in Collegiate Athletes as other researchers (4244); the current state of the evidence is not supportive of vitamin C being beneficial for athletes in general (45, 46). Merry and Ristow (47) state that, while antioxidants could play a role in recovery, vitamin C may reduce muscle hypertrophy signaling, in addition to hampering the athlete's ability to adapt to exercise training (31). For example, Paulsen et al. (43) supplemented 54 participants (28 females and 26 males), with vitamin C (1,000 mg/day) and vitamin E (235 mg/day) or a placebo for 11 weeks. The authors (43) reported that the combined vitamin C and vitamin E supplement did not improve maximal oxygen consumption (VO2max) or endurance performance after an 11-week endurance training program. Further, Paulsen et al. (44) aimed to observe if vitamin C (1,000 mg/day) and vitamin E (235 mg/day) supplementation would affect muscle growth and strength development during 11 weeks of supervised resistance training. Thirty-two resistance-trained females and males (20–45 years of age) were randomized into either a supplementor placebo group. The authors (44) reported equal increases in muscle hypertrophy between the supplemented and placebo groups. In addition, the vitamin C and vitamin E supplements interfered with protein synthesis and recovery.

In our study, we reported that Collegiate Runners had a significantly greater iron supplement intake compared to Collegiate Powerlifters. Iron supplementation has been shown to improve aerobic capacity in athletes with iron deficiency anemia (48, 49), and may be beneficial for athletes who are iron-deficient but nonameic (IDNA) (ferritin concentrations below 20 µg/L) (50, 51). The Collegiate Runner's iron supplement intake of 41.35 ± 6.53 mg/day, is similar to iron supplement intakes reported by other researchers (49, 50). For example, Pasricha et al. (49) reported iron supplementation doses ranging from 10 to 325 mg/day, for 4–24 weeks among 911 females (<18–50 years of age), 464 were given iron supplements. The authors (49) reported that iron supplementation improved exercise performance in females with iron deficiency. Similarly, Burden et al. (50) reported iron supplementation doses of one to three times per week, ranging from 10 to 425 mg/day for 6–15 weeks, in a meta-analysis on endurance athletes with IDNA. The meta-analysis included 17 studies with 443 participants (363 females and 80 males), 22.3 ± 5.1 years of age in which the researchers examined the effect of iron supplementation on VO2max. The authors (50) stated that VO2max improved with iron supplementation among athletes with IDNA. Finally, iron supplementation does not benefit athletes with a normal iron status and may lead to iron overload (48, 52).

4.2. Masters athletes

While calcium plays an important role in muscle contraction, supplementation is helpful when athletes' diets are deficient in calcium-rich foods or if they are restricting energy intake (30, 31). There is a lack of evidence on calcium supplementation's effects on athletic performance (53). Masters female athletes, took significantly more calcium supplements than Masters male athletes. We reported lower calcium supplement intakes, 494.09 ± 65.73 mg/day (females) and 187.89 ± 77.23 mg/day (males) than other researchers (5459). Shea et al. (56) supplemented 33 females (61 ± 4 years of age) with a 1,000 mg/day of calcium or a placebo either before or during one-hour of walking. The authors (56) reported that calcium supplementation before and during exercises mitigates the loss of calcium during exercise. Similarly, Barry et al. (54) supplemented 22 male cyclists (37 ± 7.6 years of age) with a 1,000 mg/day of a calcium-fortified beverage or a control beverage either before or during a 35-km time trial. The authors (54) reported that calcium supplementation did not improve time trail performance compared to the placebo. Furthermore, calcium supplementation mitigated the increase in exercise-induced parathyroid hormone, but did not affect bone resorption activity.

We reported that Masters Swimmers, had significantly higher iron intake compared to Masters General Athletes, Masters Runners, Masters Triathletes, Masters CrossFit Athletes, Masters Rowers, and Masters Cyclists. Masters Swimmers' iron supplement intake, (61.43 ± 12.10 mg/day) aligns with other researchers (19, 60). Beshgetoor and Nichols (19) reported iron supplement intakes of 43 ± 8 mg/day among Masters Athletes (25 females, 52.5 ± 2 years of age). Further, the authors (19) analyzed four-day diet records and observed that Masters Athletes who supplemented with iron actually met their daily iron intake from diet al.one. McCormick et al. (60) supplemented 31 athletes (22 females and 9 males), 20–32 years of age, with 325 mg of ferrous sulfate and 500 mg of ascorbic acid, (105 mg of elemental iron) either daily or on alternating days for eight weeks. The athletes tracked their training data (minutes, kilometers, ratings of perceived exertion), which was converted into a total training load. The authors (60) reported that daily and alternate-day supplementation increased serum iron concentrations equally; and there was no mention of performance differences between the groups. Iron has not been shown to have any performance-enhancing benefits in athletes with normal iron status, although iron has been reported to improve aerobic performance in athletes with suboptimal iron status (49, 61).

We reported a higher intake of zinc supplementation in Masters Powerlifters (47.14 ± 9.65 mg/day) than other Masters Athletes, which is inconsistent to what others have reported (62, 63). Heffernan et al. (53) noted that zinc supplementation was popular with athletes due to zinc's potential to increase testosterone concentrations, yet the evidence is limited. For example, Shafiei et al. (62) assessed how exhaustive exercise affects testosterone concentrations in cyclists who were supplemented with zinc and selenium. The 32 male cyclists were assigned to one of four groups: 30 mg/day of zinc, 200 μg/day of selenium, 30 mg/day of zinc plus 200 μg/day of selenium, or a placebo for four weeks.

The cyclists performed pre- and post-supplementation exercise testing, consisting of two-minute cycling periods, alternating between 90% and 50% of the participants maximal workload. Zinc supplementation did not significantly increase resting testosterone concentrations compared to the other groups, when all groups consumed a diet sufficient in zinc (62). Conversely, Cinar et al. (63) supplemented 40 males (18–24 years of age) with 2.5–3 mg/g/day of zinc for six weeks. There were four groups: a sedentary group (control), a sedentary group with zinc supplementation, a zinc supplementation plus resistance training group, who resistance trained four times per week, and a resistance training group (with no supplementation). The authors (63) reported that testosterone concentrations increased in all groups, except for the control group. Although, high zinc supplementation has been shown to increase testosterone in sedentary and active young men (63), the use of high dose zinc supplementation can interfere with copper absorption, causing a copper deficiency (64). Additionally, zinc supplementation is used to support the immune system after strenuous physical activity, yet the International Olympic Committee (IOC) states that there is low-moderate evidence that zinc is beneficial for immune support; alternatively, a high intake of zinc supplementation may suppress the immune system (30).

4.3. Limitations

This was a cross-sectional study, only analyzing the data at a single point in time. The Block 2005 FFQ questions about supplements are limited only to single vitamin, mineral, and multivitamin and multimineral use. Additionally, there were no questions about protein powders, sport gels/powders, pre-workout supplements, fruit and vegetable powders. We did not survey the athletes to understand why they used supplements or where they obtained their information to decide on whether to supplement or not. Further, the small sample sizes in the Collegiate and Masters Athlete sport classification groups may have affected the differences in micronutrient supplementation within and between the groups.

4.4. Conclusion

While there is extensive evidence on the knowledge about the prevalence of micronutrient supplementation among Collegiate (6, 14, 22, 65, 66) and Masters Athletes (11, 20, 67, 68), it is also important to know about the dose, frequency, duration, and other patterns of supplement use. Our study is significant because there is limited research on the analyses and patterns of micronutrient supplementation among Collegiate and Masters Athletes in various sporting groups. Because dietary supplements are frequently used by athletes, our study adds to the sparse literature on Masters Athletes and their supplementation use. The findings from our research are beneficial for understanding the patterns of micronutrient supplementation among Masters Athletes. Additionally, understanding how dietary supplements are consumed by Masters Athletes in different sports can provide insight into how to improve the performance of these athletes. The results of our study could have a positive impact on enhancing the overall performance of Masters Athletes. In addition, our research might help to increase the knowledge surrounding dietary supplement use among Masters Athletes. Further research is needed to continue evaluating supplement micronutrient intakes among different types of Collegiate and Masters Athletes. Collegiate and Masters Athletes should consult qualified nutrition professionals about supplement use. Further research should examine micronutrient supplement plus dietary micronutrient intake among Collegiate and Masters Athletes to examine the extent that athletes exceed the Recommended Dietary Allowances, and the potential effects on health and performance.

Data availability statement

The raw data supporting the conclusions of this article will be made available by the authors, without undue reservation.

Ethics statement

The studies involving human participants were reviewed and approved by Drexel University Institutional Review Board. The patients/participants provided their written informed consent to participate in this study.

Author contributions

SLV: conceptualization, supervision, and project administration. QZN: analyzed data, performed statistical analyses, wrote the manuscript. SLV: had the primary responsibility for reviewing and editing several drafts of the entire manuscript. RR and JRS: assisted with data collection. All authors contributed to the article and approved the submitted version.

Conflict of interest

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Publisher's note

All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.

References

1. Volpe SL. Micronutrient requirements for athletes. Clin Sports Med. (2007) 26(1):119–30. doi: 10.1016/j.csm.2006.11.009

PubMed Abstract | CrossRef Full Text | Google Scholar

2. Grozenski A, Kiel J. Basic nutrition for sports participation, Part 2: vitamins and minerals. Curr Sports Med Rep. (2020) 19(12):508–10. doi: 10.1249/JSR.0000000000000779

CrossRef Full Text | Google Scholar

3. Williams MH. Dietary supplements and sports performance: minerals. J Int Soc Sports Nutr. (2005) 2(1):43. doi: 10.1186/1550-2783-2-1-43

PubMed Abstract | CrossRef Full Text | Google Scholar

4. Lukaski HC. Vitamin and mineral status: effects on physical performance. Nutrition. (2004) 20(7–8):632–44. doi: 10.1016/j.nut.2004.04.001

PubMed Abstract | CrossRef Full Text | Google Scholar

5. Manore MM. Effect of physical activity on thiamine, riboflavin, and vitamin B-6 requirements. Am J Clin Nutr. (2000) 72(2):598S–606S. doi: 10.1093/ajcn/72.2.598S

PubMed Abstract | CrossRef Full Text | Google Scholar

6. Knapik JJ, Steelman RA, Hoedebecke SS, Austin KG, Farina EK, Lieberman HR. Prevalence of dietary supplement use by athletes: systematic review and meta-analysis. Sports Med Auckl Nz. (2016) 46:103–23. doi: 10.1007/s40279-015-0387-7

CrossRef Full Text | Google Scholar

7. Thomas DT, Erdman KA, Burke LM. American college of sports medicine joint position statement. Nutrition and athletic performance. Med Sci Sports Exerc. (2016) 48(3):543–68. doi: 10.1249/MSS.0000000000000852

PubMed Abstract | CrossRef Full Text | Google Scholar

8. Melina V, Craig W, Levin S. Position of the academy of nutrition and dietetics: vegetarian diets. J Acad Nutr Diet. (2016) 116(12):1970–80. doi: 10.1016/j.jand.2016.09.025

PubMed Abstract | CrossRef Full Text | Google Scholar

9. Woolf K, Manore MM. B-vitamins and exercise: does exercise alter requirements? Int J Sport Nutr Exerc Metab. (2006) 16(5):453–84. doi: 10.1123/ijsnem.16.5.453

PubMed Abstract | CrossRef Full Text | Google Scholar

10. Logue D, Madigan SM, Delahunt E, Heinen M, Mc Donnell SJ, Corish CA. Low energy availability in athletes: a review of prevalence, dietary patterns, physiological health, and sports performance. Sports Med. (2018) 48(1):73–96. doi: 10.1007/s40279-017-0790-3

PubMed Abstract | CrossRef Full Text | Google Scholar

11. Wirnitzer K, Motevalli M, Tanous DR, Gregori M, Wirnitzer G, Leitzmann C, et al. Supplement intake in recreational vegan, vegetarian, and omnivorous endurance runners—results from the NURMI study (step 2). Nutrients. (2021) 13(8):2741. doi: 10.3390/nu13082741

PubMed Abstract | CrossRef Full Text | Google Scholar

12. Lieberman HR, Marriott BP, Williams C, Judelson DA, Glickman EL, Geiselman PJ, et al. Patterns of dietary supplement use among college students. Clin Nutr. (2015) 34(5):976–85. doi: 10.1016/j.clnu.2014.10.010

PubMed Abstract | CrossRef Full Text | Google Scholar

13. Hoyte CO, Albert D, Heard KJ. The use of energy drinks, dietary supplements, and prescription medications by United States college students to enhance athletic performance. J Community Health. (2013) 38(3):575–80. doi: 10.1007/s10900-013-9653-5

PubMed Abstract | CrossRef Full Text | Google Scholar

14. Osterman S, Gray VB, Loy M, Coffey AB, Smallwood K, Barrack MT. Prioritized dietary supplement information needs of 307 NCAA division I student athletes. J Nutr Educ Behav. (2020) 52(9):867–73. doi: 10.1016/j.jneb.2020.01.007

PubMed Abstract | CrossRef Full Text | Google Scholar

15. Parnell JA, Wiens K, Erdman KA. Evaluation of congruence among dietary supplement use and motivation for supplementation in young, Canadian athletes. J Int Soc Sports Nutr. (2015) 12:49. doi: 10.1186/s12970-015-0110-y

PubMed Abstract | CrossRef Full Text | Google Scholar

16. Reaburn P, Dascombe B. Endurance performance in masters athletes. Eur Rev Aging Phys Act. (2008) 5(1):31–42. doi: 10.1007/s11556-008-0029-2

CrossRef Full Text | Google Scholar

17. Ransdell LB, Vener J, Huberty J. Masters athletes: an analysis of running, swimming and cycling performance by age and gender. J Exerc Sci Fit. (2009) 7(2):S61–S73. doi: 10.1016/S1728-869X(09)60024-1

CrossRef Full Text | Google Scholar

18. Brisswalter J, Louis J. Vitamin supplementation benefits in master athletes. Sports Med. (2014) 44(3):311–8. doi: 10.1007/s40279-013-0126-x

PubMed Abstract | CrossRef Full Text | Google Scholar

19. Beshgetoor D, Nichols JF. Dietary intake and supplement use in female master cyclists and runners. Int J Sport Nutr Exerc Metab. (2003) 13(2):166–72. doi: 10.1123/ijsnem.13.2.166

PubMed Abstract | CrossRef Full Text | Google Scholar

20. Striegel H, Simon P, Wurster C, Niess A, Ulrich R. The use of nutritional supplements among master athletes. Int J Sports Med. (2005) 27(03):236–41. doi: 10.1055/s-2005-865648

CrossRef Full Text | Google Scholar

21. Bailey RL, Gahche JJ, Miller PE, Thomas PR, Dwyer JT. Why US adults use dietary supplements. JAMA Intern Med. (2013) 173(5):355. doi: 10.1001/jamainternmed.2013.2299

PubMed Abstract | CrossRef Full Text | Google Scholar

22. Barrack MT, Muster M, Nguyen J, Rafferty A, Lisagor T. An investigation of habitual dietary supplement use among 557 NCAA division I athletes. J Am Coll Nutr. (2020) 39(7):619–27. doi: 10.1080/07315724.2020.1713247

PubMed Abstract | CrossRef Full Text | Google Scholar

23. Senekal M, Meltzer S, Horne A, Abrey NC, Papenfus L, van der Merwe S, et al. Dietary supplement use in younger and older men exercising at gyms in Cape Town. South Afr J Clin Nutr. (2021) 34(1):1–8. doi: 10.1080/16070658.2019.1628609

CrossRef Full Text | Google Scholar

24. Mazzilli M, Macaluso F, Zambelli S, Picerno P, Iuliano E. The use of dietary supplements in fitness practitioners: a cross-sectional observation study. Int J Environ Res Public Health. (2021) 18(9):5005. doi: 10.3390/ijerph18095005

PubMed Abstract | CrossRef Full Text | Google Scholar

25. El Khoury D, Hansen J, Tabakos M, Spriet LL, Brauer P. Dietary supplement use among non-athlete students at a Canadian university: a pilot-survey. Nutrients. (2020) 12(8):2284. doi: 10.3390/nu12082284

PubMed Abstract | CrossRef Full Text | Google Scholar

26. McKay AKA, Stellingwerff T, Smith ES, Martin DT, Mujika I, Goosey-Tolfrey VL, et al. Defining training and performance caliber: a participant classification framework. Int J Sports Physiol Perform. (2022) 17(2):317–31. doi: 10.1123/ijspp.2021-0451

PubMed Abstract | CrossRef Full Text | Google Scholar

27. Patlar S, Baltaci AK, Mogulkoc R. Effect of vitamin A administration on free radicals and lactate levels in individuals exercised to exhaustion. Pak J Pharm Sci. (2016) 5:1531–4.

Google Scholar

28. Teixeira VH, Valente HF, Casal SI, Marques AF, Moreira PA. Antioxidants do not prevent postexercise peroxidation and may delay muscle recovery. Med Sci Sports Exerc. (2009) 41(9):1752–60. doi: 10.1249/MSS.0b013e31819fe8e3

PubMed Abstract | CrossRef Full Text | Google Scholar

29. van der Beek EJ. Vitamin supplementation and physical exercise performance. J Sports Sci. (1991) 9(sup1):77–89. doi: 10.1080/02640419108729868

PubMed Abstract | CrossRef Full Text | Google Scholar

30. Maughan RJ, Burke LM, Dvorak J, Larson-Meyer DE, Peeling P, Phillips SM, et al. IOC Consensus statement: dietary supplements and the high-performance athlete. Br J Sports Med. (2018) 52(7):439–55. doi: 10.1136/bjsports-2018-099027

PubMed Abstract | CrossRef Full Text | Google Scholar

31. Kerksick CM, Wilborn CD, Roberts MD, Smith-Ryan A, Kleiner SM, Jäger R, et al. ISSN exercise & sports nutrition review update: research & recommendations. J Int Soc Sports Nutr. (2018) 15(1):38. doi: 10.1186/s12970-018-0242-y

PubMed Abstract | CrossRef Full Text | Google Scholar

32. Mason SA, Trewin AJ, Parker L, Wadley GD. Antioxidant supplements and endurance exercise: current evidence and mechanistic insights. Redox Biol. (2020) 35:101471. doi: 10.1016/j.redox.2020.101471

PubMed Abstract | CrossRef Full Text | Google Scholar

33. Woolf K, Hahn NL, Christensen MM, Carlson-Phillips A, Hansen CM. Nutrition assessment of B-vitamins in highly active and sedentary women. Nutrients. (2017) 9(4):329. doi: 10.3390/nu9040329

PubMed Abstract | CrossRef Full Text | Google Scholar

34. Bailey RL, Dodd KW, Gahche JJ, Dwyer JT, McDowell MA, Yetley EA, et al. Total folate and folic acid intake from foods and dietary supplements in the United States: 2003–2006. Am J Clin Nutr. (2010) 91(1):231–7. doi: 10.3945/ajcn.2009.28427

PubMed Abstract | CrossRef Full Text | Google Scholar

35. Wohlgemuth KJ, Arieta LR, Brewer GJ, Hoselton AL, Gould LM, Smith-Ryan AE. Sex differences and considerations for female specific nutritional strategies: a narrative review. J Int Soc Sports Nutr. (2021) 18(1):27. doi: 10.1186/s12970-021-00422-8

PubMed Abstract | CrossRef Full Text | Google Scholar

36. Kass LS, Skinner P, Poeira F. A pilot study on the effects of magnesium supplementation with high and low habitual dietary magnesium intake on resting and recovery from aerobic and resistance exercise and systolic blood pressure. J Sports Sci Med. (2013) 12(1):144–50.24149738

PubMed Abstract | Google Scholar

37. Córdova A, Mielgo-Ayuso J, Roche E, Caballero-García A, Fernandez-Lázaro D. Impact of magnesium supplementation in muscle damage of professional cyclists competing in a stage race. Nutrients. (2019) 11(8):1927. doi: 10.3390/nu11081927

CrossRef Full Text | Google Scholar

38. Volpe SL. Magnesium and the athlete. Curr Sports Med Rep. (2015) 14(4):279–83. doi: 10.1249/JSR.0000000000000178

PubMed Abstract | CrossRef Full Text | Google Scholar

39. Hunt G, Sukumar D, Volpe SL. Magnesium and vitamin D supplementation on exercise performance. Transl J Am Coll Sports Med. (2021) 6(4):e000179. doi: 10.1249/JSR.0000000000000178

CrossRef Full Text | Google Scholar

40. de Souza RAS, da Silva AG, de Souza MF, Souza LKF, Roschel H, da Silva SF, et al. A systematic review of CrossFit® workouts and dietary and supplementation interventions to guide nutritional strategies and future research in CrossFit®. Int J Sport Nutr Exerc Metab. (2021) 31(2):187–205. doi: 10.1123/ijsnem.2020-0223

PubMed Abstract | CrossRef Full Text | Google Scholar

41. dos Santos Quaresma MVL, Guazzelli Marques C, Nakamoto FP. Effects of diet interventions, dietary supplements, and performance-enhancing substances on the performance of CrossFit-trained individuals: a systematic review of clinical studies. Nutrition. (2021) 82:110994. doi: 10.1016/j.nut.2020.110994

PubMed Abstract | CrossRef Full Text | Google Scholar

42. Morrison D, Hughes J, Della Gatta PA, Mason S, Lamon S, Russell AP, et al. Vitamin C and E supplementation prevents some of the cellular adaptations to endurance-training in humans. Free Radic Biol Med. (2015) 89:852–62. doi: 10.1016/j.freeradbiomed.2015.10.412

PubMed Abstract | CrossRef Full Text | Google Scholar

43. Paulsen G, Cumming KT, Holden G, Hallén J, Rønnestad BR, Sveen O, et al. Vitamin C and E supplementation hampers cellular adaptation to endurance training in humans: a double-blind, randomised, controlled trial. J Physiol. (2014) 592(Pt 8):1887–901. doi: 10.1113/jphysiol.2013.267419

PubMed Abstract | CrossRef Full Text | Google Scholar

44. Paulsen G, Hamarsland H, Cumming KT, Johansen RE, Hulmi JJ, Børsheim E, et al. Vitamin C and E supplementation alters protein signalling after a strength training session, but not muscle growth during 10 weeks of training. J Physiol. (2014) 592(Pt 24):5391–408. doi: 10.1113/jphysiol.2014.279950

PubMed Abstract | CrossRef Full Text | Google Scholar

45. Ranchordas MK, Rogerson D, Soltani H, Costello JT. Antioxidants for preventing and reducing muscle soreness after exercise. Cochrane Database Syst Rev. (2017) 2017(12):CD009789. doi: 10.1002/14651858.CD009789.pub2

CrossRef Full Text | Google Scholar

46. Dutra MT, Martins WR, Ribeiro ALA, Bottaro M. The effects of strength training combined with vitamin C and E supplementation on skeletal muscle mass and strength: a systematic review and meta-analysis. J Sports Med. (2020) 2020:3505209. doi: 10.1155/2020/3505209

CrossRef Full Text | Google Scholar

47. Merry TL, Ristow M. Do antioxidant supplements interfere with skeletal muscle adaptation to exercise training? J Physiol. (2016) 594(18):5135–47. doi: 10.1113/JP270654

PubMed Abstract | CrossRef Full Text | Google Scholar

48. Zourdos MC, Sanchez-Gonzalez MA, Mahoney SE. A brief review: the implications of iron supplementation for marathon runners on health and performance. J Strength Cond Res. (2015) 29(2):559–65. doi: 10.1519/JSC.0000000000000636

PubMed Abstract | CrossRef Full Text | Google Scholar

49. Pasricha SR, Low M, Thompson J, Farrell A, De-Regil LM. Iron supplementation benefits physical performance in women of reproductive age: a systematic review and meta-analysis. J Nutr. (2014) 144(6):906–14. doi: 10.3945/jn.113.189589

PubMed Abstract | CrossRef Full Text | Google Scholar

50. Burden RJ, Morton K, Richards T, Whyte GP, Pedlar CR. Is iron treatment beneficial in iron-deficient but non-anaemic (IDNA) endurance athletes? A systematic review and meta-analysis. Br J Sports Med. (2015) 49(21):1389–97. doi: 10.1136/bjsports-2014-093624

PubMed Abstract | CrossRef Full Text | Google Scholar

51. Rubeor A, Goojha C, Manning J, White J. Does iron supplementation improve performance in iron-deficient nonanemic athletes? Sports Health. (2018) 10(5):400–5. doi: 10.1177/1941738118777488

PubMed Abstract | CrossRef Full Text | Google Scholar

52. Hinton PS. Iron and the endurance athlete. Appl Physiol Nutr Metab. (2014) 39(9):1012–8. doi: 10.1139/apnm-2014-0147

PubMed Abstract | CrossRef Full Text | Google Scholar

53. Heffernan SM, Horner K, De Vito G, Conway GE. The role of mineral and trace element supplementation in exercise and athletic performance: a systematic review. Nutrients. (2019) 11(3):696. doi: 10.3390/nu11030696

PubMed Abstract | CrossRef Full Text | Google Scholar

54. Barry DW, Hansen KC, Van Pelt RE, Witten M, Wolfe P, Kohrt WM. Acute calcium ingestion attenuates exercise-induced disruption of calcium homeostasis. Med Sci Sports Exerc. (2011) 43(4):617–23. doi: 10.1249/MSS.0b013e3181f79fa8

PubMed Abstract | CrossRef Full Text | Google Scholar

55. Sherk VD, Wherry SJ, Barry DW, Shea KL, Wolfe P, Kohrt WM. Calcium supplementation attenuates disruptions in calcium homeostasis during exercise. Med Sci Sports Exerc. (2017) 49(7):1437–42. doi: 10.1249/MSS.0000000000001239

PubMed Abstract | CrossRef Full Text | Google Scholar

56. Shea KL, Barry DW, Sherk VD, Hansen KC, Wolfe P, Kohrt WM. Calcium supplementation and parathyroid hormone response to vigorous walking in postmenopausal women. Med Sci Sports Exerc. (2014) 46(10):2007–13. doi: 10.1249/MSS.0000000000000320

PubMed Abstract | CrossRef Full Text | Google Scholar

57. Cinar V, Mogulkoc R, Baltaci AK, Bostanci O. Effects of calcium supplementation on glucose and insulin levels of athletes at rest and after exercise. Biol Trace Elem Res. (2010) 133(1):29–33. doi: 10.1007/s12011-009-8409-7

PubMed Abstract | CrossRef Full Text | Google Scholar

58. Guillemant J, Accarie C, Peres G, Guillemant S. Acute effects of an oral calcium load on markers of bone metabolism during endurance cycling exercise in male athletes. Calcif Tissue Int. (2004) 74(5):407–14. doi: 10.1007/s00223-003-0070-0

PubMed Abstract | CrossRef Full Text | Google Scholar

59. Burt MG, Mangelsdorf BL, Srivastava D, Petersons CJ. Acute effect of calcium citrate on serum calcium and cardiovascular function. J Bone Miner Res. (2013) 28(2):412–8. doi: 10.1002/jbmr.1761

PubMed Abstract | CrossRef Full Text | Google Scholar

60. McCormick R, Dreyer A, Dawson B, Sim M, Lester L, Goodman C, et al. The effectiveness of daily and alternate day oral iron supplementation in athletes with suboptimal iron status (Part 2). Int J Sport Nutr Exerc Metab. (2020) 30(3):191–6. doi: 10.1123/ijsnem.2019-0310

PubMed Abstract | CrossRef Full Text | Google Scholar

61. Low MSY, Speedy J, Styles CE, De-Regil LM, Pasricha SR. Daily iron supplementation for improving anaemia, iron status and health in menstruating women. Cochrane Database Syst Rev. (2016) 17(4):58–63. doi: 10.14529/hsm170407. Available at: https://www.readcube.com/articles/10.1002%2F14651858.cd009747.pub2 (Cited Jun 17, 2022).

Google Scholar

62. Shafiei Neek L, Gaeini AA, Choobineh S. Effect of zinc and selenium supplementation on serum testosterone and plasma lactate in cyclists after an exhaustive exercise bout. Biol Trace Elem Res. (2011) 144(1–3):454–62. doi: 10.1007/s12011-011-9138-2

PubMed Abstract | CrossRef Full Text | Google Scholar

63. Cinar V, Talaghir L, Akbulut T, Turgut M, Sarkaya M. The effects of zinc supplementation and weight training on testosterone levels. Hum Sport Med. (2017) 17(4):58–63. doi: 10.14529/hsm170407

CrossRef Full Text | Google Scholar

64. Haymes EM. Vitamin and mineral supplementation to athletes. Int J Sport Nutr. (1991) 1(2):146–69. doi: 10.1123/ijsn.1.2.146

PubMed Abstract | CrossRef Full Text | Google Scholar

65. Sobal J, Marquart LF. Vitamin/mineral supplement use among athletes: a review of the literature. Int J Sport Nutr. (1994) 4(4):320–34. doi: 10.1123/ijsn.4.4.320

PubMed Abstract | CrossRef Full Text | Google Scholar

66. El Khoury D, Dwyer JJM, Fein L, Brauer P, Brennan S, Alfaro I. Understanding the use of dietary supplements among athlete and non-athlete university students: development and validation of a questionnaire. Sports. (2019) 7(7):166. doi: 10.3390/sports7070166

PubMed Abstract | CrossRef Full Text | Google Scholar

67. Wirnitzer K, Motevalli M, Tanous DR, Gregori M, Wirnitzer G, Leitzmann C, et al. Sex differences in supplement intake in recreational endurance runners—results from the NURMI study (step 2). Nutrients. (2021) 13(8):2776. doi: 10.3390/nu13082776

PubMed Abstract | CrossRef Full Text | Google Scholar

68. Kantor ED, Rehm CD, Du M, White E, Giovannucci EL. Trends in dietary supplement use among US adults from 1999 to 2012. JAMA. (2016) 316(14):1464–74. doi: 10.1001/jama.2016.14403

PubMed Abstract | CrossRef Full Text | Google Scholar

Keywords: collegiate athletes, dietary intake, masters athletes, micronutrients, supplementation

Citation: Nichols QZ, Ramadoss R, Stanzione JR and Volpe SL (2023) Micronutrient supplement intakes among collegiate and masters athletes: A cross-sectional study. Front. Sports Act. Living 5:854442. doi: 10.3389/fspor.2023.854442

Received: 14 January 2022; Accepted: 16 February 2023;
Published: 6 April 2023.

Edited by:

Lawrence L. Spriet, University of Guelph, Canada

Reviewed by:

Tom Clifford, Loughborough University, United Kingdom
Diane DellaValle, King’s College, United States

© 2023 Nichols, Ramadoss, Stanzione and Volpe. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

*Correspondence: Stella L. Volpe c3RlbGxhbHZAdnQuZWR1

Specialty Section: This article was submitted to Sport and Exercise Nutrition, a section of the journal Frontiers in Sports and Active Living

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