Over the past 20 years, research has clearly documented the beneficial effects of nutrition on exercise performance. There is no doubt that what an athlete eats and drinks can affect health, body weight and composition, substrate availability during exercise, recovery time after exercise, and, ultimately, exercise performance. As the research and interest in sport nutrition has increased, so has the sale of ergogenic aids, supplements, herbal preparations, and diet aids, all aimed at improving sports performance. The manufacturers of these products frequently make unsubstantiated claims to entice the athlete to use their products. The athlete who wants to optimize exercise performance needs to follow good nutrition and hydration practices, use supplements and ergogenic aids carefully, minimize severe weight loss practices, and eat a variety of foods in adequate amounts.
This position is focused on adult athletes, rather than children or adolescents, and does not focus on any particular type of athlete or athletic event. Moreover, the position is intended to provide guidance to dietetics and health professionals working with athletes, and is not directed to individual athletes themselves.
It is the position of the American Dietetic Association, Dietitians of Canada, and the American College of Sports Medicine that physical activity, athletic performance, and recovery from exercise are enhanced by optimal nutrition. These organizations recommend appropriate selection of food and fluids, timing of intake, and supplement choices for optimal health and exercise performance.
The following key points summarize the current energy, nutrient, and fluid recommendations for active adults and competitive athletes noted in this position paper. Sport nutrition experts can further adjust these general recommendations to accommodate the unique concerns of individual athletes regarding health, sports, nutrient needs, food preferences, and body weight and body composition goals.
• During times of high-intensity training, adequate energy needs to be consumed to maintain body weight, maximize the training effects, and maintain health. Low-energy intakes can result in loss of muscle mass, menstrual dysfunction, loss or failure to gain bone density, and increased risk of fatigue, injury, and illness.
• Body weight and composition can affect exercise performance but should not be used as the sole criterion for participation in sports; daily weigh-ins are discouraged. Optimal body-fat levels vary depending upon the sex, age, and heredity of the athlete, as well as the sport itself. Body-fat assessment techniques have inherent variability, thus limiting the precision with which they can be interpreted. If weight loss (fat loss) is desired, it should start early—before the competitive season—and involve a trained health and nutrition professional.
• Carbohydrates are important to maintain blood-glucose levels during exercise and to replace muscle glycogen. Recommendations for athletes range from 6 to 10 g/kg body weight per day. The amount required depends upon the athlete’s total daily energy expenditure, type of sport performed, sex of the athlete, and environmental conditions.
• Protein requirements are slightly increased in highly active people. Protein recommendations for endurance athletes are 1.2 to 1.4 g/kg body weight per day, whereas those for resistance and strength-trained athletes may be as high as 1.6 to 1.7 g/kg body weight per day. These recommended protein intakes can generally be met through diet alone, without the use of protein or amino acid supplements, if energy intake is adequate to maintain body weight.
• Fat intake should not be restricted, because there is no performance benefit in consuming a diet with less than 15% of energy from fat, compared with 20% to 25% of energy from fat. Fat is important in the diets of athletes as it provides energy, fat-soluble vitamins, and essential fatty acids. Additionally, there is no scientific basis on which to recommend high-fat diets to athletes.
• The athletes at greatest risk of micronutrient deficiencies are those who restrict energy intake or use severe weight-loss practices, eliminate one or more food groups from their diet, or consume high-carbohydrate diets with low micronutrient density. Athletes should strive to consume diets that provide at least the RDAs/DRIs for all micronutrients from food.
• Dehydration decreases exercise performance; thus, adequate fluid before, during, and after exercise is necessary for health and optimal performance. Athletes should drink enough fluid to balance their fluid losses. Two hours before exercise 400 to 600 mL (14 to 22 oz) of fluid should be consumed, and during exercise 150 to 350 mL (6 to 12 oz) of fluid should be consumed every 15 to 20 min depending on tolerance. After exercise the athlete should drink adequate fluids to replace sweat losses during exercise. The athlete needs to drink at least 450 to 675 mL (16 to 24 oz) of fluid for every pound (0.5 kg) of body weight lost during exercise.
• Before exercise, a meal or snack should provide sufficient fluid to maintain hydration, be relatively low in fat and fiber to facilitate gastric emptying and minimize gastrointestinal distress, be relatively high in carbohydrate to maximize maintenance of blood glucose, be moderate in protein, and be composed of foods familiar and well tolerated by the athlete.
• During exercise, the primary goals for nutrient consumption are to replace fluid losses and provide carbohydrate (approximately 30 to 60 g per h) for the maintenance of blood glucose levels. These nutrition guidelines are especially important for endurance events lasting longer than an h, when the athlete has not consumed adequate food or fluid before exercise, or if the athlete is exercising in an extreme environment (heat, cold, or altitude).
• After exercise, the dietary goal is to provide adequate energy and carbohydrates to replace muscle glycogen and to ensure rapid recovery. If an athlete is glycogen-depleted after exercise, a carbohydrate intake of 1.5 g/kg body weight during the first 30 min and again every 2 h for 4 to 6 h will be adequate to replace glycogen stores. Protein consumed after exercise will provide amino acids for the building and repair of muscle tissue. Therefore, athletes should consume a mixed meal providing carbohydrates, protein, and fat soon after a strenuous competition or training session.
• In general, no vitamin and mineral supplements should be required if an athlete is consuming adequate energy from a variety of foods to maintain body weight. Supplementation recommendations unrelated to exercise—such as folic acid in women of childbearing potential—should be followed. If an athlete is dieting, eliminating foods or food groups, is sick or recovering from injury, or has a specific micronutrient deficiency, a multivitamin/mineral supplement may be appropriate. No single nutrient supplements should be used without a specific medical or nutritional reason (e.g., iron supplements to reverse iron deficiency anemia).
• Athletes should be counseled regarding the use of ergogenic aids, which should be used with caution and only after careful evaluation of the product for safety, efficacy, potency, and legality.
• Vegetarian athletes may be at risk for low energy, protein, and micronutrient intakes because of high intakes of low- energy–dense foods and the elimination of meat and dairy from the diet. Consultation with a registered dietitian will help to avoid these nutrition problems.
Meeting energy needs is the first nutrition priority for athletes. Achieving energy balance is essential for the maintenance of lean tissue mass, immune and reproductive function, and optimum athletic performance. Energy balance is defined as a state when energy intake (the sum of energy from food, fluids, and supplement products) equals energy expenditure (the sum of energy expended as basal metabolism, the thermic effect of food, and any voluntary physical activity) (139). Inadequate energy intake relative to energy expenditure compromises performance and the benefits associated with training. With limited energy intake, fat and lean tissue mass will be used by the body for fuel. Loss of muscle results in the loss of strength and endurance. In addition, chronically low energy intake often results in poor nutrient intake, particularly of the micronutrients.
In the 1989 Recommended Dietary Allowances (RDAs) (112), mean energy requirements for women and men who are slightly to moderately active and between 19 to 50 yr of age were established as 2,200 and 2,900 kcal per day, respectively. Expressed alternatively, normally active people are counseled to consume an energy intake of 1.5 to 1.7 times resting energy expenditure or at a rate of 37 to 41 kcal/kg body weight per day (112). Energy expenditure is influenced by heredity, age, sex, body size, fat-free mass, and the intensity, frequency, and duration of exercise. For athletes, the recommendation is made to evaluate the kind of exercise performed for its intensity, frequency, and duration, and then to add this increment to the energy needed for normal daily activity (109,97,59). For example, a 70 kg male runner who runs 10 miles per day at a 6-min pace would require approximately 1,063 kcal per day to cover the energy expenditure of running (0.253 kcal·min-1/kg) (78), plus the energy cost of normal daily activities (70 kg × 37 to 41 kcal/kg body weight) for normal activity. Thus, this athlete would need approximately 3,653 to 3,933 kcal per day to cover the total cost of energy expenditure. Ultimately, however, numeric guidelines for energy intake, such as those cited above, can only provide a crude approximation of the average energy needs of an individual athlete. Any athlete needs to consume enough energy to maintain appropriate weight and body composition while training for a sport. Usual energy intakes for male endurance athletes range from 3,000 to 5,000 kcal per day (56). Although usual energy intakes for many intensely training female athletes may match those of male athletes per kg of body weight, some consume less energy than they expend. This low-energy intake can lead to weight loss and disruption of reproductive function, and is often seen with energy intakes of less than 1,800 to 2,000 kcal per day (78, 56, 48, 75, 90, 93).
Although resistance exercise usually requires less energy than endurance exercise, the total energy needs of athletes participating in strength training and bodybuilding may be as high as those of endurance athletes because of their increased body size and high levels of fat-free mass. In circumstances in which an increase in lean body mass is the goal, energy intake must be sufficient to meet the needs for muscle growth. Thus, many strength athletes may need 44 to 50 kcal/kg body weight/d, and those in serious training may have even higher energy requirements (more than 50 kcal/kg body weight/d) (79, 98).
It is often the case that an athlete will want to increase or decrease body weight to meet the demands of a sport. In either case, weight change should be accomplished slowly during the off-season, or at the beginning of the season, before competition begins. Weight gain can be accomplished by the incorporation of additional energy into the diet (500 to 1,000 kcal per day) in conjunction with increased strength training to promote the accretion of the tissue desired. How quickly weight gain occurs will depend on the athlete’s genetic makeup, degree of positive energy balance, number of rest and recovery days per week, and type of exercise training program. Weight loss is somewhat more problematic, as diminished energy intake can compromise nutrient intake and exercise performance while decreasing both body fat and muscle mass (141,95).
Consultation with a registered dietitian trained in sport nutrition can help athletes maintain a healthful diet while reducing total energy intake to allow gradual weight loss (approximately 1 to 2 lbs/wk or 0.5 to 1.0 kg/wk). The process begins with the identification of what constitutes a realistic, healthful body weight based on genetic, physiologic, social, sport, and psychological factors. A healthful weight is one that can be realistically maintained, allows for positive advances in exercise performance, minimizes the risk of injury or illness, and reduces the risk factors for chronic disease. Table 1 shows strategies to help health professionals work with athletes to identify and maintain healthful body weights.
Failure to meet weight-loss goals may result in severe consequences, such as being cut from the team, restricted participation, or elimination from competition. This may result in chronic dieting by many athletes to maintain lower-than-healthful body weights, which in turn can lead to disordered eating and, in severe cases, clinical eating disorders. Nutrition strategies for identification, intervention, and treatment of eating disorders in athletes have been presented elsewhere (152, 22, 138, 142).
When pressure to achieve a weight goal is high, athletes are likely to attempt any weight-loss method to achieve success, regardless of the health consequences. Weight loss can be especially problematic for female athletes who generally are smaller, and thus may have lower energy needs than male athletes. In women, low-energy intake, in conjunction with high-energy output, has been associated with alterations in the secretion of the pituitary gonadotropins (luteinizing hormone [LH] and follicle-stimulating hormone [FSH]) (90,58). This, in turn, results in changes in ovarian hormone secretions leading to amenorrhea and loss of (or failure to gain) bone mass in young female athletes (5). It has been proposed that energy availability (amount of energy intake unused after energy for activity has been provided) determines the health of the body, and that curtailing energy intake to attain some body weight or fat standard may result in insufficient energy being available to maintain all vital functions (48, 90, 47). Thus, a negative energy balance, due to chronic dieting or undereating in conjunction with heavy exercise may alter the energy flux and create a negative “energy drain,” which compromises reproductive function and bone health. Incorporation of additional energy into the diets of these women has resulted in the return of menstrual function and the improvement in overall nutritional status (48, 80). Although failure of reproductive function in male athletes has not been extensively investigated, Loucks (89) has identified changes in LH and FSH secretion in men that mimic those of women in response to changes in energy availability.
Body composition and weight are 2 of the many factors that contribute to optimal exercise performance. Taken together, these 2 factors may affect an athlete’s potential for success within a given sport. Body weight can influence an athlete’s speed, endurance, and power, whereas body composition can affect an athlete’s strength, agility, and appearance. Most athletes require a high strength-to-weight ratio to achieve optimal athletic performance, and because body fat adds to weight without adding to strength, low body fat percentages are often emphasized within many sports (123). However, too little body fat results in deterioration of health and performance (47, 65). Athletic performance cannot be accurately predicted based solely on body weight and composition (64).
The primary reason for determining an athlete’s body composition is to obtain information that may be beneficial in improving athletic performance (10). Therefore, the determination of an athlete’s optimal body weight and composition for health and competition should be done individually, because these factors are strongly influenced by age, sex, genetics, and the requirements of the sport. Yet, some sports dictate that athletes make changes in body weight and composition that may not be optimal for the athlete. For example, weight-class sports—such as wrestling or lightweight rowing—may require athletes to lose or gain weight to qualify for a specific weight category. Sports with an esthetic component—such as dance, gymnastics, and figure skating—may pressure athletes to lose weight and body fat to have a lean physique, although their current weight for health and performance may be optimal. With extreme energy restrictions, both muscle and fat mass are lost, which may adversely influence an athlete’s performance. Thus, an athlete’s optimal competitive body weight and relative body fatness should be determined when an athlete is healthy and performing at his or her best (147).
Body Composition and Sport Performance
Percentage of body fat values for athletes varies depending on the sex of the athlete and the sport itself. Male athletes with the lowest estimates of body fat (less than 6%) include middle-distance and long-distance runners and bodybuilders, whereas male basketball players, cyclists, gymnasts, sprinters, jumpers, triathletes, and wrestlers average between 6% to 15% body fat (65, 135). Male athletes involved in power sports such as football, rugby, and ice and field hockey have slightly more variable body fat levels (6% to 19%). Female athletes with the lowest estimates of body fat (6% to 15%) participate in bodybuilding, cycling, triathlons, and running events; higher fat levels are found in female athletes participating in racquetball, skiing, soccer, swimming, tennis, and volleyball (10% to 20%) (65, 135). The estimated minimal level of body fat compatible with health is 5% for males and 12% for females (84); however, optimal body fat percentages for an individual athlete may be much higher than these minimums and should be determined on an individual basis. Athletes who strive to maintain body weight or body fat levels that are inappropriate, or have body-fat percentages below these minimal levels, may be at risk for an eating disorder or other health problems related to poor energy and nutrient intakes (48, 93, 138, 47, 80, 11, 12, 92).
Assessment of Body Composition
Methods for assessment of body composition are based on either a 2-component or a multicomponent model and use several different measurement techniques. Two-component models divide the body into either fat mass (all lipids within the body) or fat-free mass (the remainder of lipids after fat is subtracted). The multicomponent model divides the body into 3 or more components. For example, the 3-component model divides the body into fat mass and 2 components of fat-free mass (bone mineral and lean tissue). The criterion methods most commonly used to assess components of body composition in athletes are based on a 2-component or a multicomponent model. Though a multicomponent criterion model is preferred for assessing body composition because it provides more accurate estimates, measurement techniques required for this model are not readily available to most athletes. A 2-component criterion model typically uses hydrodensitometry (hydrostatic weighing) or plethysmography (BODPOD) measurement techniques, and a 3-component model uses dual-energy x-ray absorptiometry (DEXA) measurements. The most common methods used to measure body composition in field or clinical settings include anthropometry (skinfolds), bioelectrical impedance analysis (BIA), and near-infrared interactance. These field methods are validated using either 2-component or multicomponent criterion models (86). When using these field methods, care should be taken in choosing the appropriate validated prediction equation for estimating body composition based on an athlete’s demographics (age, sex, level of adiposity, ethnicity, and physical activity) in order to obtain accurate estimates (62).
The relative validity of any body composition field method depends on its accuracy compared with the criterion method and its reliability (reproducibility) (84). DEXA and hydrostatic weighing (hydrodensitometry) are 2 widely used criterion methods from which field methods of body composition assessment for athletes are developed (55, 85, 107, 130, 50, 66). Regardless of the method used, athletes and coaches should know the errors associated with the body composition assessment method being used. With carefully applied skin-fold or BIA methods, it is possible to estimate relative body fat percentage with an error of 3% to 4%, and to estimate fat-free mass within 2.5 to 3.5 kg (64, 84, 86). Thus, if the actual body fat percentage is 15%, then predicted values could range from 12% to 18% (assuming a 3% error). If the actual fat-free mass is 50 kg, then predicted values could range from 47.5 to 52.5 kg, assuming an error of 2.5 kg. If inappropriate prediction equations for a method are used, poor measurement techniques applied or if the measurement equipment is poorly maintained and calibrated, the errors associated with the body composition estimate will be much larger. Because of the errors associated with body composition assessment methods, it is inappropriate to set a specific body-fat percentage goal for an individual athlete. Instead, a range of target percentage of body-fat values should be recommended.
MACRONUTRIENT REQUIREMENTS FOR EXERCISE
The fuel burned during exercise depends on the intensity and duration of the exercise performed, the sex of the athlete, and prior nutritional status. All other conditions being equal, an increase in the intensity of an exercise will increase the contribution of carbohydrate to the energy pool (20, 21). As the length of the exercise continues, the source of this carbohydrate may shift from the muscle glycogen pool to circulating blood glucose, but in all circumstances, if blood glucose cannot be maintained, the intensity of the exercise performed will decrease (39). Fat contributes to the energy pool over a wide range of exercise intensities, being metabolized at somewhat the same absolute rate throughout the range; however, the proportion of energy contributed by fat decreases as exercise intensity increases because the contribution of carbohydrate increases (17). Protein contributes to the energy pool at rest and during exercise, but in fed individuals it probably provides less than 5% of the energy expended (49,121). As the duration of exercise increases, protein may contribute to the maintenance of blood glucose through gluconeogenesis in the liver. In experiments in which subjects are tested in a fasting state, the contribution of fat to the energy pool will be greater than in people who are tested postprandially when exercise performed is moderate (approximately 50% of maximal oxygen uptake [&OV0312;O2max]) (16). With exercise of higher intensity (greater than 65% of &OV0312;O2max), neither prior feeding nor training markedly affects the fuel used (16).
Data are not presently available, however, to suggest that athletes need a diet substantially different from that recommended in the Dietary Guidelines for Americans (116) or the Nutrition Recommendations for Canadians (16) (55% to 58% of energy from carbohydrate, 12% to 15% of energy from protein and 25% to 30% of energy from fat). Although high-carbohydrate diets (more than 60% of energy intake) have been advocated in the past, the use of proportions in making dietary recommendations may actually be misleading in terms of providing optimum nutrition. When energy intake is 4,000 to 5,000 kcal per day, even a diet containing 50% of the energy from carbohydrate will provide 500 to 600 g of carbohydrate (or approximately 7 to 8 g/kg for a 70 kg athlete), which is sufficient to maintain muscle glycogen stores from day to day (36,38). Similarly, if protein intake in such a diet was even as low as 10% of energy intake, absolute protein intake (100 to 125 g per day) would exceed the recommendations for protein intake for athletes (1.2 to 1.7 g per day or 84 to 119 g in a 70 kg athlete, see the following discussion on nitrogen balance in men). Conversely, when energy intake is less than 2,000 kcal per day, even a diet providing 60% of the energy from carbohydrate may not provide sufficient carbohydrate to maintain optimal carbohydrate stores (4 to 5 g/kg in a 60 kg athlete). Typically, diets containing 20–25% energy from fat have been recommended to facilitate adequate carbohydrate intake and to assist in weight management where necessary. Thus, specific recommendations for individual energy components may be more useful when they are based on body size, weight and body composition goals, the sport being performed, and sex of the athlete.
Protein needs of athletes have received considerable investigation, not only in regard to whether athletes’ protein requirements are increased, but also in relation to whether individual amino acids are a benefit to performance. Mechanisms suggested to increase athletes’ protein requirements include the need to repair exercise-induced microdamage to muscle fibers, use of small amounts of protein as an energy source for exercise, and the need for additional protein to support gains in lean tissue mass (28,82). If protein needs are increased, the magnitude of the increase may depend on the type of exercise performed (endurance vs resistance), the intensity and duration of the activity, and possibly the sex of the participants.
For endurance athletes, nitrogen balance studies in men suggest a protein recommendation of 1.2 g/kg per day (105). Little information is available regarding requirements of endurance athletes who are women. Resistance exercise is thought to increase protein requirements even more than endurance exercise, and it has been recommended that experienced male bodybuilders and strength athletes consume 1.6 to 1.7 g/kg body weight per day to allow for the accumulation and maintenance of lean tissue (82, 140). Again, data on female strength athletes are not available. Athletes should be aware that increasing protein intake beyond the recommended level is unlikely to result in additional increases in lean tissue because there is a limit to the rate at which protein tissue can be accrued (28), whereas other sources have suggested an intake of 1.2 to 1.4 g/kg per day (82). It must be ensured that energy intake is adequate—otherwise, protein will be used as an energy source, falsely elevating estimates of the requirements under conditions of energy balance. It is worth noting that the customary diets of most athletes provide sufficient protein to cover even the increased amounts that may be needed (56).
The use of individual amino acids to enhance performance has also been studied. One proposal is that administration of branched chain amino acids (BCAA) may enhance endurance performance by delaying the onset of central nervous system fatigue (41). It has also been proposed that BCAA may extend performance by serving as substrates for energy expenditure (30). The results of human studies, however, have been inconsistent (19, 106, 143, 91). Because the safety and efficacy of these mixtures has not been established, their use cannot be advocated.
Some studies (111, 81) have proposed a positive effect of relatively high-fat diets (more than 70% of energy intake) on athletic performance. Careful evaluation of these studies show little evidence supporting this concept (73). Fat is a necessary component of a normal diet, providing energy and essential elements of cell membranes and associated nutrients such as vitamins E, A, and D. However, the long-term negative effects of high-fat diets on health are well known. The Dietary Guidelines for Americans and Nutrition Recommendations for Canadians make recommendations for the proportion of energy from fatty acids (10% saturated, 10% polyunsaturated, 10% monounsaturated) (116, 61). Athletes should follow these general recommendations, and should also ensure that their fat intakes are not excessively low. The 1999 study by Dreon and colleagues (46) suggests that there are negative effects on blood lipid profiles in some people when total dietary fat intake is less than 15% of energy.
VITAMINS AND MINERALS
Micronutrients play an important role in energy production, hemoglobin (Hb) synthesis, maintenance of bone health, adequate immune function, and the protection of body tissues from oxidative damage. They are also required to help build and repair muscle tissue following exercise. Theoretically, exercise may increase or alter the need for vitamins and minerals in a number of ways. Exercise stresses many of the metabolic pathways in which these micronutrients are required, thus exercise training may result in muscle biochemical adaptations that increase micronutrient needs. Exercise may also increase the turnover of these micronutrients, thus increasing loss of micronutrients from the body. Finally, higher intakes of micronutrients may be required to cover increased needs for the repair and maintenance of the lean tissue mass in athletes. It is assumed that the current RDAs and Dietary Reference Intakes (DRIs) are appropriate for athletes unless otherwise stated (112,67,68). Athletes at the greatest risk of poor micronutrient status are those who restrict energy intake or use severe weight-loss practices, eliminate one or more of the food groups from their diet, or consume high-carbohydrate, low-micronutrient–dense diets. Athletes participating in these types of behaviors may need to use a multivitamin and mineral supplement to improve overall micronutrient status. Supplementation with single micronutrients is discouraged unless clear medical, nutritional, or public health reasons are present, such as the supplementation of iron to treat iron deficiency anemia or folic acid to prevent birth defects.
The B-complex vitamins have 2 major functions directly related to exercise. Thiamin, riboflavin, vitamin B-6, niacin, pantothenic acid, and biotin are involved in energy production during exercise (97,35,83,94,120,129,104), whereas folate and vitamin B-12 are required for the production of red cells, protein synthesis, and in tissue repair and maintenance (104). Limited research has examined whether exercise increases the need for some of the B-complex vitamins, especially vitamin B-6, riboflavin, and thiamin (35,83,120,104,96). Available data were not sufficiently precise to set separate recommendations for athletes or to quantitatively link recommendations to energy expenditure (68). Nevertheless, the data available suggest that exercise may slightly increase the need for these vitamins perhaps up to twice the current recommended amount (94). These increased needs can generally be met by the higher energy intakes required of athletes to maintain body weight.
The antioxidant nutrients—such as vitamins A, E, and C, beta carotene, and selenium—play an important role in protecting the cell membranes from oxidative damage. Because exercise can increase oxygen consumption by 10- to 15-fold, it has been hypothesized that chronic exercise produces a constant “oxidative stress” on the muscles and other cells (34,74). In addition, muscle-tissue damage caused by intense exercise can lead to lipid peroxidation of membranes. Although there is some evidence that acute exercise may increase levels of lipid peroxide by-products (76), habitual exercise has been shown to result in an augmented antioxidant system and a reduction of lipid peroxidation (34). Thus, a well-trained athlete may have a more developed endogenous antioxidant system than a sedentary person (77). Research examining whether exercise increases the need for the antioxidant nutrients is equivocal and controversial; thus, there is no clear consensus on whether supplementation of antioxidant nutrients is necessary (34, 76,77). The lack of consensus is especially true for the athlete with adequate or above-adequate blood levels of the antioxidant vitamins (34). Those athletes at greatest risk for poor antioxidant intakes are athletes following a low-fat diet, those who restrict energy intakes, or those with limited dietary intakes of fruits and vegetables.
The primary minerals low in the diets of athletes—especially female athletes—are calcium, iron, and zinc (93,60). Low intakes of these minerals can usually be attributed to energy restriction or avoidance of animal products such as meat, fish, poultry, and dairy products. Calcium is especially important for the building and repair of bone tissue and the maintenance of blood calcium levels. Inadequate dietary calcium increases the risk of low bone mineral density (BMD) and stress fractures. Female athletes are at greatest risk for low BMD if energy intakes are low, dairy products are eliminated from the diet, and menstrual dysfunction is present (48,47). Vitamin D is also required for adequate calcium absorption, regulation of serum calcium levels, and promotion of bone health. The 2 primary sources of vitamin D are fortified foods, such as milk, and the production of vitamin D by ultraviolet conversion in the skin. Athletes who live at northern latitudes or who train primarily indoors throughout the year—such as gymnasts and figure skaters—may be at risk for poor vitamin D status, especially if foods fortified with vitamin D are not consumed (14). These athletes would benefit from vitamin D supplementation at the level of the DRI (5 μg/d or 200 international units [IU] vitamin D) (67).
Iron plays an important role in exercise as it is required for the formation of Hb and myoglobin, which bind oxygen in the body, and for enzymes involved in energy production. Iron depletion (low iron stores) is one of the most prevalent nutrient deficiencies observed in athletes, especially female athletes. The impact of iron depletion on exercise performance is limited, but if this condition progresses to iron deficiency anemia (low Hb levels), exercise performance can be negatively affected (97,60).
The high incidence of iron depletion in athletes is usually attributed to poor energy intakes; avoidance of meat, fish, and poultry that contain iron in the readily available heme form; vegetarian diets that have poor iron bioavailability; or increased iron losses in sweat, feces, urine, or menstrual blood. Athletes—especially females, long-distance runners, and vegetarians—should be screened periodically to assess iron status. Changes in iron storage (low-serum ferritin concentrations) will occur first, followed by low-iron transport (low-serum iron concentrations), and eventually iron deficiency anemia (low Hb and hematocrit (Hct) concentrations). Because reversal of iron deficiency anemia can require 3 to 6 months, it is advantageous to begin nutrition interventions before iron deficiency anemia can develop. Although depleted iron stores are more prevalent in female athletes, the incidence of iron deficiency anemia in female athletes is similar to the 9% to 11% found in the general female population (60,87).
A transient decrease in ferritin and Hb may be experienced by some athletes at the initiation of training. These decreases are the result of an increase in plasma volume, which causes hemodilution and appears to have no negative effect on performance (60). If an athlete appears to have iron deficiency anemia but does not respond to nutrition intervention, then low Hb values may be the result of changes in plasma volume, and not poor nutritional status (97). Chronic iron deficiency anemia resulting from poor iron intake can seriously affect health and exercise performance and needs medical and nutrition intervention.
In the United States, it is estimated that the zinc content of the food supply is approximately 12.3 mg of zinc per person, with 70% of the zinc coming from animal products (37). Based on survey data, approximately 90% of men and 81% of women have zinc intakes that are below the 1989 RDAs (15 mg and 12 mg, respectively) (110). This nutritional shortfall is also seen in athletes, particularly females (93). The impact of these low zinc intakes on zinc status is difficult to measure, because clear assessment criteria have not been established and plasma zinc concentrations may not reflect changes in whole-body zinc status (88). Because of the role zinc plays in growth, building and repair of muscle tissue, and energy production, it is prudent to assess the diets of active females for adequate zinc intake.
Exercise performance is optimal when athletes maintain fluid balance during exercise; conversely, exercise performance is impaired with progressive dehydration (8,13,102,108,146). Moreover, dehydration increases the risk of potentially life-threatening heat injury such as heat stroke (115). Accordingly, athletes should attempt to remain well-hydrated before and during exercise.
The American College of Sports Medicine Position Stand on Exercise and Fluid Replacement (4) and the National Athletic Trainers’ Association (NATA) Position Statement on Fluid Replacement for Athletes (32) provide comprehensive overviews of the research and recommendations on maintaining hydration during exercise. The following information summarizes the key points from these position stands and provides recommendations for special environmental conditions.
Water and Electrolyte Balance
• Losses during exercise
Athletes dissipate the metabolic heat produced during physical activity by radiation, conduction, convection, and by vaporization of water. In hot, dry environments, evaporation accounts for more than 80% of metabolic heat loss. Sweat rates will vary depending on variables such as body size, exercise intensity, ambient temperature, humidity, and acclimation, but can exceed 1.8 kg (approximately 1,800 mL) per h (4). In addition to water, sweat also contains substantial amounts of sodium (an average of approximately 50 mmol·L-1, or about 1 g·L-1, although concentrations vary widely), modest amounts of potassium, and small amounts of minerals such as iron and calcium.
• Gastric emptying and intestinal absorption of fluids during exercise
Euhydration (and the associated maintenance of physiological function and performance) can be accomplished during exercise only if the rate of fluid ingestion and absorption equals the rate of fluid loss through sweating (and, in events of longer duration, urination). Fluid balance during exercise is not always possible because maximal sweat rates exceed maximal gastric emptying rates, which in turn limit fluid absorption. In most cases, however, rates of fluid ingestion by athletes during exercise fall short of amounts that could be emptied from the stomach and absorbed by the gut. For example, athletes often consume less than 500 mL per h during competition (4), whereas gastric emptying rates of more than 1 L per h are possible (4).
Gastric emptying is maximized when the amount of fluid in the stomach is high. It is reduced with hypertonic fluids or when carbohydrate concentration is greater than or equal to 8%; however, fluids containing 4% to 8% carbohydrate can generally be emptied at over 1 L per h in most people when gastric volume is maintained at or above 600 mL (4,32).
• Dehydration, hypohydration, and hyponatremia
Disturbances of fluid and electrolyte balance that can occur in athletes include dehydration, hypohydration, and hyponatremia (7). In their most severe forms, all can be life-threatening. Exercise-induced dehydration develops as a consequence of fluid losses that exceed fluid intake. In contrast, hypohydration occurs when athletes dehydrate themselves before beginning a competitive event, and can be induced by prior fluid restriction, exercise practices, diuretic use, or sauna exposure. In most cases, hypohydration is practiced by athletes competing in sports with weight categories (e.g., wrestling, boxing, lightweight crew, weight lifting, and judo). Hyponatremia (low blood-sodium concentrations of less than 130 mmol·L-1) can develop either as a result of prolonged, heavy sweating with failure to replace sodium, or when excess water is retained in the body (9). Although endurance athletes are more likely to suffer from dehydration than from overhydration, the latter is not uncommon. For example, 11 of 605 athletes entered in the New Zealand Ironman triathlon developed severe hyponatremia, and 8 of these athletes were likely overhydrated, as they had either maintained or gained up to 5% of body weight during the race (136).
Fluid and Electrolyte Recommendations
• Before exercise
Athletes should be well-hydrated when beginning to exercise. In addition to drinking generous amounts of fluid in the 24 h before an exercise session, the ACSM and the NATA recommend drinking 400 to 600 mL of fluid 2–3 h before exercise (4,32). Such a practice should optimize hydration status while allowing enough time for any excess fluid to be excreted as urine before beginning to exercise.
• During exercise
Athletes should attempt to drink enough fluid to maintain fluid balance, as even partial dehydration can compromise performance. If fluid balance cannot be maintained, the maximal amounts that can be tolerated should be ingested. Optimal hydration can be facilitated by drinking 150 to 350 mL (6 to 12 oz) of fluid at 15- to 20-min intervals, beginning at the start of exercise (4).
Beverages containing carbohydrate in concentrations of 4% to 8% are recommended for intense exercise events lasting longer than 1 h (4). These beverages are also suitable for hydration during exercise events lasting less than 1 h, although plain water is appropriate under these conditions.
There appears to be little physiologic need to replace electrolytes during a single exercise session of moderate duration (e.g., less than 3 to 4 h), particularly if sodium was present in the previous meal. However, including sodium in amounts between 0.5 and 0.7 g·L-1 is recommended during exercise lasting longer than 1 h because it may enhance palatability and the drive to drink, therefore increasing the amount of fluid consumed (4). It should be noted that this amount of sodium exceeds that typically available in commercial beverages. Including sodium in fluid replacement beverages may also help prevent hyponatremia in susceptible people (4,145). Although most athletes who drink more fluid than they lose as sweat simply excrete the excess fluid as urine, in some people it is retained (136). If the fluid contains sodium, it could help prevent the dilution of serum sodium levels, thereby decreasing the risk of hyponatremia. Limiting fluid intake so that it does not exceed sweat rate can also decrease risk of hyponatremia.
• After exercise
In most cases, athletes do not consume enough fluids during exercise to balance fluid losses, and thus complete their exercise sessions dehydrated to some extent. Consuming up to 150% of the weight lost during an exercise session may be necessary to cover losses in sweat plus obligatory urine production (134). Including sodium either in or with fluids consumed postexercise reduces the diuresis that occurs when only plain water is ingested (32,99). Sodium also helps the rehydration process by maintaining plasma osmolality and thereby the desire to drink. Because most commercial sport drinks do not contain enough sodium to optimize postexercise fluid replacement, athletes can rehydrate in conjunction with a sodium-containing meal (100). High-sodium items include soups, pickles, cheeses, processed meats, pizza, pretzels, and popcorn. Use of condiments such as soy sauce and ketchup, as well as salting food at the table, also increase sodium intake.
Special Environmental Conditions
• Hot and humid environments
The risks of dehydration and heat injury increase dramatically in hot, humid environments (3). If the ambient temperature exceeds body temperature, heat cannot be dissipated by radiation. Moreover, if the relative humidity is high, the potential to dissipate heat by evaporation of sweat is substantially reduced—at a relative humidity of 100%, vaporization of sweat does not occur. Instead, in humid environments, sweat drips from the body, leading to nonfunctional fluid loss. When temperature and humidity are both high, there is a very high risk of heat illness, and competitive events should be postponed, rescheduled, or canceled (34,3). If competitive events do occur under these conditions, every precaution should be taken to assure that athletes are well hydrated, have ample access to fluids, and are monitored for heat-related illness (32).
• Cold environments
Although the risk of dehydration is greater in hot environments, dehydration is not uncommon in cool or cold weather (1). Factors that could contribute to dehydration under these conditions include respiratory fluid losses in cold dry environments, as well as sweat losses that may be high if insulated clothing is worn during intense exercise. Dehydration could also occur as a result of low rates of fluid ingestion: if an athlete is chilled and available fluids are cold, the incentive to drink would clearly be reduced. Finally, the difficulty of removing multiple layers of clothing to urinate may cause some athletes, especially women, to voluntarily limit their fluid intake (54).
Exposure to altitudes higher than 2,500 m (8,200 ft) may result in fluid losses beyond those associated with any exercise that might be performed. These losses are the result of mandatory diuresis and high respiratory water losses, accompanied by decreased appetite, which lead to an increased need for fluid intake. The diuresis is considered by some to be an indication of successful acclimatization (57), although others (27) have suggested that at least part of the diuresis can be minimized by adequate energy intake and maintenance of body weight. Under circumstances of weight maintenance, this diuresis is of a magnitude of about 500 mL per day and lasts for about 7 d (27). Respiratory water losses may be as high as 1,900 mL per day in men (29) and 850 mL in women (101). Thus, fluid intake at high altitude should be increased to as much as 3 to 4 L per day to assure optimal kidney function.
THE TRAINING DIET
Recommendations for athletes’ intakes of energy, macronutrients, vitamins, and minerals are described elsewhere in this document. These recommendations are often presented in terms of milligram or gram amounts of nutrients (e.g., 6 to 10 g carbohydrate/kg body weight) and must be translated into food choices consistent with food preferences and training schedules of athletes (125). The foundations (proportion of energy from protein, fat, and carbohydrate) for the training diets of athletes, however, do not differ substantively from current recommendations for the general population. Thus, the training diet should incorporate the principles outlined in the Dietary Guidelines for Americans (116) and Canada’s Guidelines for Healthy Eating (117), and be based on the 1992 U.S. food guide (U.S. Food Guide Pyramid) (52) or the 1992 Canadian food guide (Canada’s Food Guide to Healthy Eating (31)).
The fundamental differences between an athlete’s diet and that of the general population are that athletes require additional fluid to cover sweat losses and additional energy to fuel physical activity. As discussed earlier, it is appropriate for much of the additional energy to be supplied as carbohydrate. Though in some cases needs for other nutrients also increase (e.g., protein, B-complex vitamins), the proportional increase in energy requirements appear to exceed the proportional increase in needs for other nutrients. Accordingly, as energy requirements increase, athletes should first aim to consume the maximum number of servings specified in both food guides from carbohydrate-based food groups (breads, cereals and grains, vegetables, and fruits). For many athletes, however, energy needs will exceed the amount of energy (kcal per day) in the upper range of servings for these food groups as provided by both food guides. To maintain dietary variety, these athletes may also increase the number and/or size of servings of dairy products and protein foods, but should aim to keep the proportions of energy provided by different food groups consistent with those identified in both food guides. Conversely, athletes who are small and/or have lower energy needs will need to pay greater attention to making nutrient-dense food choices to obtain adequate carbohydrate, protein, and micronutrients.
The other issue that arises in a discussion of the diet of athletes relates to the timing of meals and snacks. Common sense dictates that food and fluid intake around workouts needs to be determined on an individual basis and will depend, in part, on an athlete’s gastrointestinal characteristics as well as the intensity of the workout. For example, an athlete might tolerate a snack consisting of milk and a sandwich 1 h before a low-intensity workout, but would be uncomfortable if the same meal was consumed before a very hard effort. In any case, athletes in heavy training or doing multiple daily workouts may need to eat more than 3 meals and 3 snacks per day and should consider every possible eating occasion (15). For example, they should consider eating in close proximity to the end of a workout, having more than one afternoon snack, or eating a substantial snack before bed.
Eating before exercise, as opposed to exercising in the fasting state, has been shown to improve performance (113,133,152). The meal or snack consumed before competition or an intense workout should prepare athletes for the upcoming activity, and leave him or her neither hungry nor with undigested food in the stomach. Accordingly, the following general guidelines for meals and snacks should be used: sufficient in fluid to maintain hydration, low in fat and fiber to facilitate gastric emptying and minimize gastrointestinal distress, high in carbohydrate to maintain blood glucose and maximize glycogen stores, moderate in protein, and composed of foods familiar to the athlete.
The size and timing of the preexercise meal are interrelated. Because most athletes do not like to compete on a full stomach, smaller meals should be consumed in closer proximity to the event to allow for gastric emptying, whereas larger meals can be consumed if more time is available before exercise or competition. Amounts of carbohydrate used in studies in which performance was enhanced have ranged from approximately 200 to 300 g carbohydrate for meals consumed 3 to 4 h before exercise (113,133,152,132). The recommendations on carbohydrate consumption within 1 h before activity have been controversial. Early research suggested that this practice leads to hypoglycemia and premature fatigue (53); however, more recent studies report either no effect or beneficial effects of preevent feeding on performance (38,113,2,44,63). Current data are mixed concerning whether the glycemic index of carbohydrate in the preexercise meal affects performance (143,148).
Although the above guidelines are sound and work well on average, the individual needs of the athlete must be emphasized. For example, some athletes consume and enjoy a substantial meal (e.g., pancakes, juice, and scrambled eggs) 2 to 4 h before exercise or competition; however, others may suffer severe gastrointestinal distress following such a meal and need to rely on liquid meals. Athletes should always ensure that they know what works best for themselves by experimenting with new foods and beverages during practice sessions and planning ahead to ensure they will have access to these foods at the appropriate time.
Whether or not carbohydrate consumption in amounts typically provided in sport drinks (4% to 8%) improves performance in events lasting 1 h or less has been controversial. Current research now supports the benefit of this practice (13,137,6,72,71,42,114), especially in athletes who exercise in the morning after an overnight fast when liver glycogen levels are low. Thus, providing exogenous carbohydrate under these conditions would help maintain blood glucose levels and improve performance. Accordingly, performance advantages in short-duration activities may not be apparent when exercise is done in the nonfasting state.
For longer events, consuming 0.7 g carbohydrate/kg body weight per h (approximately 30 to 60 g per h) has been shown unequivocally to extend endurance performance (36). Consuming carbohydrates during exercise is even more important in situations when athletes have not carbohydrate-loaded, consumed preexercise meals, or restricted energy intake for weight loss. Carbohydrate intake should begin shortly after the onset of activity; consuming a given amount of carbohydrate as a bolus after 2 h of exercise is not as effective as consuming the same amount at 15- to 20-min intervals during the first 2 h of activity (103). The carbohydrate consumed should yield primarily glucose; fructose alone is not as effective and may lead to diarrhea, although mixtures of glucose and fructose seem to be effective (36). If the same total amount of carbohydrate and fluid is ingested, the form of carbohydrate does not seem to matter—some athletes may prefer to use a sport drink whereas others may prefer to eat a solid or gel and consume water. As described elsewhere in this document, adequate fluid intake is also essential for maintaining endurance performance.
The timing and composition of the postcompetition or postexercise meal or snack depend on the length and intensity of the exercise session (i.e., whether glycogen depletion occurred), and when the next intense workout will occur. For example, most athletes will finish a marathon with depleted glycogen stores, whereas glycogen depletion would be much less marked following a 90-min training run. However, most athletes competing in a marathon in the morning will not be doing another race or hard workout in the afternoon. Timing and composition of the postexercise meal are thus less critical for these athletes. Conversely, a triathlete participating in a 90-min run in the morning and a 3-h cycling workout in the afternoon needs to maximize recovery between training sessions, and the postworkout meal assumes considerable importance in meeting this goal.
Timing of postexercise carbohydrate intake affects glycogen synthesis over the short term. Consumption of carbohydrates beginning immediately after exercise (1.5 g carbohydrate/kg at 2-h intervals is often recommended) results in higher glycogen levels at 6 h postexercise than when ingestion is delayed for 2 h (69,70). The highest reported rates of postexercise glycogen synthesis occurred in individuals fed 0.4 g carbohydrate/kg every 15 min for 4 h after glycogen-depleting exercise (45). It should be noted that this represents a very high-energy load (almost 2,000 kcal for a 75-kg athlete) that may exceed the energy expended during the exercise session itself.
The above practices regarding timing of ingestion do not need to be adhered to by athletes who take one or more days between intense training sessions, because when sufficient carbohydrate is provided over a 24-h period, the timing of intake does not appear to affect the amount of glycogen stored (23). Nevertheless, consuming a meal or snack in close proximity to the end of exercise may be important for athletes to meet daily carbohydrate and energy goals.
The type of carbohydrate consumed can also affect postexercise glycogen synthesis. When comparing simple sugars, glucose and sucrose appear equally effective when consumed at a rate of 1.5 g/kg body weight for 2 h; fructose alone is less effective (18). With regard to whole foods, consumption of carbohydrates with a high glycemic index results in higher muscle glycogen levels 24 h after exercise as compared with the same amount of carbohydrates provided as foods with a low glycemic index (25). The usefulness of these findings, however, must be considered in conjunction with the athlete’s overall diet, and should likely be reserved for occasions when maximizing postexercise glycogen synthesis is critical.
When isocaloric amounts of carbohydrates or carbohydrates plus protein and fat are provided following endurance (24) or resistance (127) exercise, glycogen synthesis rates are similar. Accordingly, in contrast to what was suggested in earlier research (154), adding protein does not appreciably enhance glycogen repletion. Nevertheless, including protein in a postexercise meal may provide needed amino acids for muscle protein repair and promote a more anabolic hormonal profile (128).
SUPPLEMENTS AND ERGOGENIC AIDS
The marketing of ergogenic aids (items claiming to increase work output or performance) is an international, multimillion dollar business that preys on the desires of athletes to be the best, and when one item does not work or is discredited by research, another comes along to take its place. Nutrition-related ergogenic aids are particularly problematic. In the United States, the Dietary Supplement Health and Education Act of 1994 (119) allows supplement manufacturers to make claims regarding the effect of products on the structure/function of the body, as long as they do not claim to “diagnose, mitigate, treat, cure, or prevent” a specific disease. As long as a special supplement label indicates the active ingredients and the entire ingredient list is provided, claims for enhanced performance—be they valid or not—can be made. The advent of the Internet means that a greater variety of products are more readily available, increasing the pressure on the experts to keep up-to-date on both the science and the claims of ergogenic aids (144).
THE VEGETARIAN ATHLETE
Some athletes choose to follow vegetarian diets. Nutrition recommendations for these athletes should be formulated with consideration of the effects of both vegetarianism and exercise. The position of the American Dietetic Association on vegetarian diets (124) provides appropriate dietary guidance that should be considered in conjunction with the information provided herein.
Vegetarianism does not necessarily affect energy needs, though energy availability could be reduced slightly if a vegetarian has an extremely high fiber intake. As with all athletes, monitoring body weight and composition is the preferred means of determining if energy needs are satisfied. Some people—especially women—may switch to vegetarianism as a means of restricting energy intake to attain the lean body habitus favored in some sports. Occasionally, this may be a step toward development of an eating disorder (118). Because of this association, coaches and trainers should be alert when an athlete becomes vegetarian, and ensure that appropriate weight is maintained.
Studies consistently report that vegetarians have lower protein intakes than omnivores. Although the protein quality of a vegetarian diet is adequate for adults (112,61,153), plant proteins are not as well-digested as animal proteins (112). Thus, to adjust for incomplete digestion, an increase of about 10% in the amount consumed may be made (112). Accordingly, recommended protein intakes for vegetarian athletes would be about 1.3 to 1.8 g/kg body weight, using recommendations for athletes as a baseline (38,28,140). Vegetarian athletes with relatively low energy intakes may need to choose foods carefully to ensure that their protein intakes are consistent with these recommendations.
Vegetarian athletes may be at risk for low intakes of vitamins B-12 and D, riboflavin, iron, calcium, and zinc, because many of these nutrients are high in animal products. Iron is a nutrient that may be of particular concern to vegetarian athletes. Because of the lower bioavailability of iron in plant-based diets, the iron stores in vegetarians are generally lower than those of omnivores, despite total iron intakes that are similar or even higher (40). When combined with data indicating that exercise may increase iron requirements, it is possible that vegetarian athletes, especially women, may be at greater risk of developing poor iron status. Accordingly, it would be prudent for iron status to be monitored routinely in female vegetarian athletes.
ROLES AND RESPONSIBILITIES OF HEALTH CARE PROFESSIONALS
Every competitive and recreational athlete needs adequate fuel, fluids, and nutrients to perform at their best. It is the role of the sports nutrition expert to advise athletes regarding appropriate nutrition needs before, during, and after exercise, and for the maintenance of good health and optimal body weight and composition. Qualified health and nutrition professionals can help athletes and active people in the following ways:
• Educate athletes about energy requirements for their sport and the role of food in fueling the body. Discourage unrealistic weight and body composition goals and emphasize the importance of adequate energy intake for good health, prevention of injury, and exercise performance.
• Assess the body size and composition of an athlete for the determination of an appropriate weight and composition for the sports in which he or she participates. Provide the athlete with nutritionally sound techniques for maintaining an appropriate body weight and composition without the use of fad or severe diets. Undue pressure on athletes for weight loss or the maintenance of a lean body build can increase the risk of restrictive eating behaviors, and in extreme cases lead to a clinical eating disorder.
• Assess the athlete’s typical dietary and supplement intake during training, competition, and the off-season. Use this assessment to provide appropriate recommendations for energy and nutrient intakes for the maintenance of good health, appropriate body weight and composition, and optimal sport performance throughout the year. Give specific guidelines for making good food and fluid selections while traveling and eating away from home.
• Assess the fluid intake and weight loss of athletes during exercise and make appropriate recommendations regarding total fluid intake and fluid intake before, during, and after exercise. Help athletes to determine appropriate types and amounts of beverages to use during exercise, especially if the athlete is exercising in extreme environments.
• For athletes such as the vegetarian athlete with special nutrition concerns, provide appropriate nutrition guidelines to assure adequate intakes of energy, protein, and micronutrients.
• Carefully evaluate any vitamin/mineral or herbal supplements, ergogenic aids, or performance-enhancing drugs an athlete wants to use. These products should be used with caution and only after a careful review of their legality and the current literature pertaining to the ingredients listed on the product label; these products should not be recommended until after evaluating the athlete’s health, diet, nutrition needs, current supplement and drug use, and energy requirements.
All nutrition recommendations for athletes should be based on current scientific data and the needs of athletes as individuals. Health care professionals should work with athletes, coaches, and family members to build rapport and to provide athletes with the best-possible environment for meeting sports-related nutrition goals.
• ADA/DC/ACSM position adopted by the ADA House Executive Committee on July 12, 2000; approved by Dietitians of Canada on July 12, 2000; and approved by the American College of Sports Medicine Board of Trustees on October 17, 2000. This position is in effect until December 31, 2005. The American Dietetic Association, Dietitians of Canada, and the American College of Sports Medicine, authorize the publication of the position, in its entirety, provided full and proper credit is given. Requests for used portions of the position, must be directed to ADA Headquarters at 800/877–1600, ext 4896, or [email protected]
• Recognition is given to the following for their contributions:
–American Dietetic Association: Melinda M. Manore, PhD, RD, FACSM (Arizona State University, Tempe, AZ)
–Dietitians of Canada: Susan I. Barr, PhD, RDN, FACSM (University of British Columbia, Vancouver, BC)
–American College of Sports Medicine: Gail E. Butterfield, PhD, RD, FACSM (Dr. Butterfield passed away on December 27, 1999. This position is dedicated to her contributions in the field of nutrition and sports medicine).
–American Dietetic Association: Nancy Clark, MS, RD, FACSM (SportsMedicine Brookline, Brookline, MA); Susan M. Kleiner, PhD, RD (High Performance Nutrition, Mercer Island, WA); Suzanne Nelson, DSc (University of Washington, Seattle, WA); Stella Volpe, PhD, RD, FACSM (University of Massachusetts, Amherst, MA).
–Dietitians of Canada: Maryilyn Booth, MSc, RD (private practice, Ontario, Canada); Susie Langley, MS, RD (private practice, Ontario, Canada); Heidi Smith, BSc, RD (University of Guelph, Ontario, Canada); Heather Schmurr, RD (private practice, Alberta, Canada).
–American College of Sports Medicine: Elizabeth Applegate, PhD, FACSM (University of California-Davis, Davis, CA); Nancy Clark, MS, RD, FACSM (SportsMedicine Brookline, Brookline, MA); Linda Houtkooper, PhD, RD (University of Arizona, Tucson, AZ); William J. Kraemer, PhD, FACSM (Ball State University, Muncie, IN); Scott Powers, PhD, FACSM (University of Florida, Gainesville); Janice Thompson, PhD, FACSM (University of New Mexico, Albuquerque).
1. Adner, M. M., J. J. Scarlet, J. Casey, W. Robison, B. H. Jones. The Boston marathon medical care team: ten years of experience. Physician Sportsmed. 16: 98–106, 1988.
2. Alberici, J. C., P. A. Farrell, P. M. Kris-Etherton, C. A. Shively. Effects of pre-exercise candy bar ingestion on glycemic response, substrate utilization, and performance. Int. J. Sport Nutr. 3: 323–333, 1993.
3. American College of Sports Medicine. Position Stand: Heat and cold illnesses during distance running. Med. Sci. Sports Exerc.
4. American College of Sports Medicine. Position Stand: Exercise and fluid replacement. Med. Sci. Sports Exerc.
5. American College of Sports Medicine. Position Stand: The Female Athlete Triad. Med. Sci. Sports Exerc.
6. Ball T. C., S. A. Headley, P. M. Vanderburgh, J. C. Smith. Periodic carbohydrate replacement during 50-min of high-intensity cycling improves subsequent sprint performance. Int. J. Sport Nutr. 5: 151–158, 1995.
7. Barr SI. Effects of dehydration on exercise performance. Can. J. Appl. Physiol. 24: 164–172, 1999.
8. Barr S. I., D. L. Costill, W. J. Fink. Fluid replacement during prolonged exercise: Effects of water, saline, or no fluid. Med. Sci. Sports Exerc. 23: 811–817, 1991.
9. Barr S. I., D. L. Costill. Water. Can the endurance athlete get too much of a good thing? J. Am. Diet Assoc.
10. Barr S. I., L. J. McCargar, S. M. Crawford. Practical use of body composition analysis in sport. Sports Med. 17: 277–282, 1994.
11. Beals, K. A., M. M. Manore. Nutritional status of female athletes with subclinical eating disorders. J. Am. Diet Assoc. 98: 419–425, 1998.
12. Beals, K. A., M. M. Manore. Subclinical eating disorders in physically active women. Topics Clin. Nutr. 14: 14–29, 1999.
13. Below, P. R., R. Mora-Rodriguez, J. Gonzalez-Alonso, E. F. Coyle. Fluid and carbohydrate ingestion independently improve performance during 1 h of intense exercise. Med. Sci. Sports Exerc. 27: 200–210, 1995.
14. Benardot D. Working with young athletes: views of a nutritionist on a sports medicine team. Int. J. Sport Nutr. 6: 110–120, 1996.
15. Benardot, D., W. R. Thompson. Energy from food for physical activity. Enough and on time. ACSM Health & Fitness J. 3: 14–18, 1999.
16. Bergman, B. C., G. A. Brooks. Respiratory gas-exchange ratios during graded exercise in fed and fasted trained and untrained men. J. Appl. Physiol. 86: 479–487, 1999.
17. Bergman, B. C., G. E. Butterfield, E. E. Wolfel, G. A. Casazza, G. D. Lopaschuk, G. A. Brooks. Evaluation of exercise and training on muscle lipid metabolism. Am. J. Physiol.
18. Blom, P. C. S., A. T. Hostmark, O. Vaage, K. R. Kardel, S. Maehlum. Effect of different post-exercise sugar diets on the rate of muscle glycogen synthesis. Med. Sci. Sports Exerc.
19. Blomstrand, E., P. Hassmen, B. Ekblom, E. A. Newsholme. Administration of branched-chain amino acids during sustained exercise: effects on performance and on plasma concentration of some amino acids. Eur. J. Appl. Physiol. 63: 83–88, 1991.
20. Brooks, G. A., J. Mercier. Balance of carbohydrate and lipid utilization during exercise. The cross over concept. J. Appl. Physiol. 76: 2253–2261, 1994.
21. Brooks, G. A., J. Trimmer. Literature supports the cross over concept [letter]. J. Appl. Physiol. 80: 1073–1075, 1995.
22. Brownell, K. D., J. Rodin, J. H. Wilmore. Eating, Body Weight, and Performance in Athletes: Disorders of Modern Society. Philadelphia, Pa: Lea & Febiger; 1992.
23. Burke, L. M., G. R. Collier, P. G. Davis, P. A. Fricker, A. J. Sanigorski, M. Hargreaves. Muscle glycogen storage after prolonged exercise: effect of the frequency of carbohydrate feedings. Am. J. Clin. Nutr. 64: 115–119, 1996.
24. Burke, L. M., G. R. Collier, S. K. Beasley, P. G. Davis, P. A. Fricker, P. Heeley, K. Walder, M. Hargreaves. Effect of coingestion of fat and protein with carbohydrate feedings on muscle glycogen storage. J. Appl. Physiol. 78: 2187–2192, 1995.
25. Burke, L. M., G. R. Collier, M. Hargreaves. Muscle glycogen storage after prolonged exercise: Effect of the glycemic index of carbohydrate feeding. J. Appl. Physiol. 75: 1019–1023, 1993.
26. Butterfield GE. Ergogenic Aids: Evaluating sport nutrition products. Int. J. Sport Nutr. 6: 191–197, 1996.
27. Butterfield GE. Maintenance of Body Weight at Altitude: In Search of 500 kcal/day. In: Marriott BM, Carlson SJ, eds. Nutritional Needs in Cold and High-Altitude Environments.
Washington, DC: Committee on Military Nutrition Research; 1996, pp. 357–378.
28. Butterfield GE. Whole-body protein utilization in humans. Med. Sci. Sports Exerc. 19 (suppl): S157–S165, 1987.
29. Butterfield, G. E., J. Gates, S. Fleming, G.A. Brooks, J. R. Sutton, J. T. Reeves. Increased energy intake minimizes weight loss in men at high altitude. J. Appl. Physiol. 72: 1741–1748, 1992.
30. Calders, P., D. Matthys, W. Derave, J-L. Pannier. Effect of branched-chain amino acids (BCAA), glucose, and glucose plus BCAA on endurance performance in rats. Med. Sci. Sports Exerc. 31: 583–587, 1999.
31. Canada’s Food Guide to Healthy Eating. Ottawa, Canada. Minister of Supply and Services Canada; 1992.
32. Casa, D. J., L. E. Armstrong, S. K. Hillman, S. J. Montain, R. V. Reiff, B. S. E. Rich, W. O. Roberts, J. A. Stone. National Athletic Trainers’ Association Position Statement. Fluid replacement for athletes. J. Athletic Training. 35 (2): 212–224, 2000.
33. Clark N. Nutrition quackery: when claims are too good to be true. Physician Sportsmed. 23: 7–8, 1995.
34. Clarkson PM. Antioxidants and physical performance. Critical Rev. Food Sci. Nutr. 35(1&2): 131–141, 1995.
35. Clarkson PM. Exercise and the B vitamins. In: Wolinsky I, ed. Nutrition in Exercise and Sports.
3rd ed. Boca Raton, Fla: CRC Press; 179–195, 1998.
36. Coggan, A. R., E. F. Coyle. Carbohydrate ingestion during prolonged exercise: effects on metabolism and performance. In: Holloszy JO, ed. Exerc Sports Sci Rev
. Philadelphia, Pa: Williams & Wilkins; 19;1–40, 1991.
37. Cousins RJ. Zinc. In: Ziegler EE, Filer LJ. Eds. Present Knowledge in Nutrition. 7th ed. Washington, DC: ILSI Press; 1996:293–306.
38. Coyle EF. Substrate utilization during exercise in active people. Am. J. Clin. Nutr. 61 (suppl): 968S-79S, 1995.
39. Coyle, E. F., A. R. Coggan, M. K. Hemmert, J. L. Ivy. Muscle glycogen utilization during prolonged strenuous exercise when fed carbohydrate. J. Appl. Physiol. 61: 165–172, 1986.
40. Craig WJ. Iron status of vegetarians. Am. J. Clin. Nutr 59 (suppl): 1233S-1237S, 1994.
41. Davis, J. M., S. P. Bailey. Possible mechanisms of central nervous system fatigue during exercise. Med. Sci. Sports Exerc. 29: 45–57, 1997.
42. Davis, J. M., D. A. Jackson, M. S. Broadwell, J. L. Queary, C. L. Lambert. Carbohydrate drinks delay fatigue during intermittent, high-intensity cycling in active men and women. Int. J. Sports Med. 7: 261–273, 1997.
43. DeMarco, H. M., K. P. Sucher, C. J. Cisar, G. E. Butterfield. Pre-exercise carbohydrate meals: application of glycemic index. Med. Sci. Sports Exerc. 31: 164–170, 1999.
44. Devlin, J. T., J. Calles-Escandon, E. S. Horton. Effects of preexercise snack feedings on endurance cycle exercise. J. Appl. Physiol. 60: 980–985, 1986.
45. Doyle, A. J., W. H. Sherman, R. L. Strauss. Effects of eccentric and concentric exercise on muscle glycogen replenishment. J. Appl. Physiol. 74: 1848–1855, 1993.
46. Dreon, D. M., H. A. Fernstrom, P. T. Williams, R. M. Krauss. A very low-fat diet is not associated with improved lipoprotein profiles in men with a predominance of large low-density lipoproteins. Am. J. Clin. Nutr. 69: 411–418, 1999.
47. Dueck, C. A., M. M. Manore, K. S. Matt. Role of energy balance in athletic menstrual dysfunction. Int. J. Sport Nutr. 6: 165–190, 1996.
48. Dueck, C. A., K. S. Matt, M. M. Manore, J. S. Skinner. Treatment of athletic amenorrhea with a diet and training intervention program. Int. J. Sport Nutr. 6: 24–40, 1996.
49. El-Khoury, A. E., A. Forslund, R. Olsson, S. Branth, A. Sjodin, A. Andersson, A. Atkinson, A. Selvaraj, L. Hambraeus, and V. R. Young. Moderate exercise at energy balance does not affect 24-h leucine oxidation or nitrogen retention in healthy men. Am. J. Physiol. 273: E394–E407, 1997.
50. Ellis, K. J., S. A. Abrams, W. W. Wong. Body composition of a young, multiethnic female population. Am. J. Clin. Nutr. 65: 724–31, 1997.
51. Engels HJ. Publication of adverse events in exercise studies involving nutritional agents. Int. J. Sport Nutr. 9: 89–91, 1999.
52. Food Guide Pyramid: A Guide to Daily Food Choices. Washington, DC: US Dept of Agriculture, Human Nutrition Information Service; 1992:Home and Garden Bulletin No.252.
53. Foster, C., D. L. Costill, W. J. Fink. Effects of preexercise feedings on endurance performance. Med. Sci. Sports. 11: 1–5, 1979.
54. Freund, B. J., M. N. Sawka. Influence of cold stress on human fluid balance. In: Marriott BM, Carlson SJ, eds. Nutritional Needs in Cold and in High-Altitude Environments.
Washington, DC: Committee on Military Nutrition Research; 161–179, 1996.
55. Going SB. Densitometry. In: Human Body Composition. In: Roche AF, Heymsfield SB, Lohman TG, eds. Champaign, Ill: Human Kinetics; 1996, pp. 3–23.
56. Grandjean AC. Diets of elite athletes: Has the discipline of sports nutrition made an impact? J. Nutr. 127 (suppl): 874S-877S, 1997.
57. Hackett, P. H., D. Rennie, R. F. Grover, J. T. Reeves. Acute mountain sickness and the edemas of high altitude: a common pathogenesis? Respir Physiol. 46: 383–390, 1981.
58. Harber VJ. Menstrual dysfunction in athletes: an energetic challenge. Exerc. Sport Sci. Rev. 28: 19–23, 2000.
59. Hawley, J., L. Burke. Peak Performance: Training and Nutritional Strategies for Sports. St Leonards, NWS: Allen & Unwin Publishers; 1998.
60. Haymes, E. M., P. M. Clarkson. Minerals and trace minerals. In: Berning JR, Steen SN, eds. Nutrition for Sport and Exercise
. Gaithersburg, Md: Aspen Publishers, 1998, pp. 77–107.
61. Health, and Welfare Canada. Nutrition Recommendations: The Report of the Scientific Review Committee
. Ottawa, Canada: Can. Government Publishing Centre; 1990.
62. Heyward VH. Evaluation of body composition. Curr Issues Sports Med. 22: 146–156, 1996.
63. Horowitz, J. F., E. F. Coyle. Metabolic responses to pre-exercise meals containing various carbohydrates and fat. Am. J. Clin. Nutr. 58: 235–241, 1993.
64. Houtkooper LB. Body composition. IN: Manore MM, Thompson JL. Sport Nutrition for Health and Performance. Champaign, Ill: Human Kinetics Publisher 2000:pp.199–219.
65. Houtkooper, L. B., S. B. Going. Body composition: how should it be measured? Does it affect sport performance? Sports Sci. Exchange. 7: 1–8, 1994.
66. Houtkooper, L. B., S. B. Going, J. Sproul, R. M. Blew, T. G. Lohman. Comparison of methods for assessing body composition changes over 1 year in postmenopausal women. Am. J. Clin. Nutr. 72: 4001–4006, 2000.
67. Institute of Medicine. Dietary reference intakes. Calcium, phosphorus, magnesium, vitamin D, and fluoride. Washington, DC: National Academy Press; 1997.
68. Institute of Medicine. Dietary reference intakes. Thiamin, riboflavin, niacin, vitamin B-6, folate, vitamin B-12, pantothenic acid, biotin, and choline. Washington, DC: National Academy Press; 1998.
69. Ivy, J. L., A. L. Katz, C. L. Cutler, W. M. Sherman, E. F. Coyle. Muscle glycogen synthesis after exercise: effect of time of carbohydrate ingestion. J. Appl. Physiol. 64: 1480–1485, 1988.
70. Ivy, J. L., M. C. Lee, J. T. Brozinick Jr., M. J. Reed. Muscle glycogen storage after different amounts of carbohydrate ingestion. J. Appl. Physiol. 65: 2018–2023, 1988.
71. Jeukendrump, A. E., F. Brouns, A. J. M. Wagenmakers, W. H. M. Sarris. Carbohydrate-electrolyte feedings improve 1 h time trial cycling performance. Int. J. Sports Med. 18 (2): 125–129, 1997.
72. Jeukendrup, A. E., R. Jentjens. Oxidation of carbohydrate feedings during prolonged exercise. Current thoughts, guidelines and directions for future research. Sports Med. 29 (6): 407–424, 2000.
73. Jeukendrup, A. E., W. H. M. Saris. Fat as a fuel during exercise. In: Berning JR, Steen SN, eds. Nutrition for Sport and Exercise
. Gaithersburg, Md: Aspen Publishers; 59–76, 1998.
74. Ji LL. Oxidative stress during exercise: implication of antioxidant nutrients. Free Radical Biology & Med. 18: 1079–1086, 1995.
75. Jonnalagadda, S. S., D. Benardot, M. Nelson. Energy and nutrient intakes of the United States national women’s artistic gymnastics team. Int. J. Sport Nutr. 8: 331–344, 1998.
76. Kanter MM. Free radicals, exercise, and antioxidant supplementation. Int. J. Sport Nutr. 4: 205–220, 1994.
77. Kanter MM. Nutritional antioxidants and physical activity. In: Wolinsky I, ed. Nutrition in Exercise and Sport
. Boca Raton, Fla: CRC Press; 245–255, 1998.
78. Katch, F. I., W. D. McArdle. Introduction to Nutrition, Exercise, and Health
. 4th ed. Philadelphia, Pa: Lea & Febiger; 1993.
79. Kleiner, S. M., L. H. Calabrese, K. M. Fielder, H. K. Naito, C. I. Skibinski. Dietary influences on cardiovascular disease risk in anabolic steroid-using and nonusing bodybuilders. J. Am. Coll Nutr. 8: 109–119, 1989.
80. Kopp-Woodroffe, S. A., M. M. Manore, C. A. Dueck, J. S. Skinner, K. S. Matt. Energy and nutrient status of amenorrheic athletes participating in a diet and exercise training intervention program. Int. J. Sport Nutr. 9: 70–88, 1999.
81. Lambert, E. V., D. P. Speechly, S. C. Dennis, T. D. Noakes. Enhanced endurance in trained cyclists during moderate intensity exercise following 2 weeks adaptation to a high fat diet. Eur. J. Appl. Physiol. 69: 287–293, 1994.
82. Lemon PWR. Effects of exercise on dietary protein requirements. Int. J. Sport Nutr. 8: 426–447, 1998.
83. Lewis RD. Riboflavin and niacin. In: Wolinsky I, Driskell JA, eds. Sports Nutrition: Vitamins and Trace Elements. Boca Raton, Fla: CRC Press; 1997, pp. 57–73.
84. Lohman TG. Basic Concepts in body composition assessment. Advances in Body Composition Assessment
. Champaign, Ill: Human Kinetics Publisher; 109–118:1992.
85. Lohman TG. Dual energy x-ray absorptiometry. In: Roche AF, S.B. Heymsfield SB, Lohman TG, eds. Human Body Composition
. Champaign, Ill: Human Kinetics; 1996, pp. 63–78.
86. Lohman, T. G., L. B. Houtkooper, S. B. Going. Body fat measurement goes high-tech. Not all are created equal. ACSM Health Fitness J. 1: 30–35, 1997.
87. Looker, A. C., P. R. Dallman, M. D. Carroll, E. W. Gunter, C. L. Johnson. Prevalence of iron deficiency in the United States. JAMA. 277: 973–976, 1997.
88. Loosli AR. Reversing sports-related iron and zinc deficiencies. Phys. Sports Med. 21: 70–76, 1993.
89. Loucks AB. Dietary energy requirements of physically active men and women: Threshold effects on reproductive function. In: Reducing Stress Fractures in Physically Active Military Women. Committee on Military Nutrition Research, Subcommittee on Body Composition, Nutrition and Health of Military Women
. Washington, DC: National Academy Press; 1998, p. 89.
90. Loucks, A. B., G. A. Laughlin, J. F. Mortola, L. Girton, J. C. Nelson, S. S. C. Yen. Hypothalamic-pituitary-thyroidal function in eumenorrheic and amenorrheic athletes. J. Clin. Endocrinol Metab. 75: 514–518, 1992.
91. Madsen, K., D. A. MacLean, B. Kiens, D. Christensen. Effects of glucose, glucose plus branched-chain amino acids, or placebo on bike performance over 100 km. J. Appl. Physiol. 81: 2644–2650, 1996.
92. Manore MM. Chronic dieting in active women: What are the health consequences? Women’s Health Issues. 6: 332–341, 1996.
93. Manore MM. Nutritional needs of the female athlete. In: Wheeler KB, Lombardo JA, eds. Clinics in Sports Medicine: Nutritional Aspects of Exercise
. Philadelphia, Pa: WB Saunders Company; 549–563, 1999.
94. Manore MM. The effect of physical activity on thiamin, riboflavin, and vitamin B-6 r, riboflavin, and vitamin B-6 requirements. Am. J. Clin. Nutr. 72 (suppl): 5985–6065, 2000.
95. Manore MM. The overweight athlete. In: Maughan R, ed. IOC Encyclopedia of Sports Medicine: Nutrition in Sport
. Oxford, United Kingdom: Blackwell Science Publishers; 1999, pp. 469–483.
96. Manore MM. Vitamin B6 and exercise. Int. J. Sport Nutr. 4: 89–103, 1994
97. Manore, M. M., J. L. Thompson. Sport Nutrition for Health and Performance
. Champaign, Ill: Human Kinetics; 2000.
98. Manore, M. M., J. Thompson, M. Russo. Diet and exercise strategies of a world-class bodybuilder. Int. J. Sport Nutr. 3: 76–86, 1993.
99. Maughan, R. J., J. B. Leiper. Sodium intake and post-exercise rehydration in man. Eur. J. Appl. Physiol. 71: 311–319, 1995.
100. Maughan, R. J., J. B. Leiper, S. M. Shirreffs. Restoration of fluid balance after exercise-induced dehydration: Effects of food and fluid intake. Eur. J. Appl. Physiol. 73: 317–325, 1996.
101. Mawson, J. T., B. Braun, P. B. Rock, L. G. Moore, R. Mazzeo, G. E. Butterfield. Women at altitude: Energy requirements at 4300 m. J. Appl. Physiol. 88: 272–281, 2000.
102. McConnell, G. K., C. M. Burge, S. L. Skinner, M. Hargreaves. Influence of ingested fluid volume on physiological responses during prolonged exercise. Acta Physiol. Scan. 160: 149–156, 1997.
103. McConnell, G. K., K. Kloot, M. Hargreaves. Effect of timing of carbohydrate ingestion on endurance exercise performance. Med. Sci. Sports Exerc. 28: 1300–1304k 1996.
104. McMartin K. Folate and vitamin B12. In: Wolinsky I, Driskell JA, eds. Sports Nutrition: Vitamins and Trace Elements
. Boca Raton, Fla: CRC Press; 85–96, 1997.
105. Meredith, C. N., M. J. Zackin, W. R. Frontera, W. J. Evans. Dietary protein requirements and body protein metabolism in endurance-trained men. J. Appl. Physiol. 66: 2850–2856 1989.
106. Mittleman, K. D., M. R. Ricci, S. P. Bailey. Branched-chain amino acids prolong exercise during heat stress in men and women. Med. Sci. Sports Exerc. 30: 83–91, 1998.
107. Modlesky, C. M., E. M. Evans, M. L. Millard-Stafford, M. A. Collins, R. D. Lewis, and K. J. Cureton. Impact of bone mineral estimates on percent fat estimates from a four-component model. Med. Sci. Sports Exerc. 31: 1861–1868, 1999.
108. Montain, S. J., E. F. Coyle. Influence of graded dehydration on hyperthermia and cardiovascular drift during exercise. J. Appl. Physiol. 73: 1340–1350, 1992.
109. Montoye, H. J., H. C. G. Kemper, W. H. M. Saris, R. A. Washburn. Measuring Physical Activity and Energy Expenditure.
Champaign, IL: Human Kinetics Publication; 1996.
110. Moser-Veillon PB. Zinc. consumption patterns and dietary recommendations. J. Am. Diet Assoc. 90: 1089–1093, 1990.
111. Muoio, D. M., J. J. Leddy, P. J. Horvath, A. B. Awad, D. R. Pendergast. Effect of dietary fat on metabolic adjustments to maximal VO2 and endurance in runners. Med. Sci. Sports Exerc. 26: 81–88, 1994.
112. National Research Council. Recommended Dietary Allowances.
10th ed. Washington, DC: National Academy Press; 1989.
113. Neufer, P. D., D. L. Costill, M. G. Flynn, J. P. Kirwan, J. B. Mitchell, J. Houmard. Improvements in exercise performance: Effects of carbohydrate feedings and diet. J. Appl. Physiol. 62: 983–988 1987.
114. Nicholas, C.W., C. Williams, H. K. A. Lakomy, G. Phillips, A. Nowitz. Influence of ingesting a carbohydrate-electrolyte solution on endurance capacity during intermittent, high-intensity shuttle running. J. Sports Sci. 13: 283–290, 1995.
115. Noakes TD. Fluid replacement during exercise. Exerc. Sport Sci. Rev. 21: 297–330, 1993.
116. Nutrition, and Your Health. Dietary Guidelines for Americans
. 4th ed. US Depts of Agriculture and Health and Human Services; 1995. Home and Garden Bulletin No. 232.
117. Nutrition Recommendations.... A Call for Action: Summary Report of the Scientific Review Committee and the Communications/Implementation Committee.
Ottawa, Canada: Health and Welfare Canada; 1989.
118. O’Connor, M. A., S. W. Touyz, S. M. Dunn, P. J. V. Beumont. Vegetarianism in anorexia nervosa? A review of 116 consecutive cases. Med. J. Aust. 147: 540–542, 1987.
119. 103rd Congress. Public law 103–417. Dietary Supplements Health and Education Act of 1994. (21USC 3419(r)(6)), 1994.
120. Peifer JJ. Thiamin. In: Wolinsky I, Driskell JA, eds. Sports Nutrition: Vitamins and Trace Elements
. Boca Raton, Fla: CRC Press; 47–55:1997.
121. Phillips, S. M., S. A. Atkinson, M. A. Tarnopolsky, and J. D. Macdougall. Gender differences in leucine kinetics and nitrogen balance in endurance athletes. J. Appl. Physiol. 75: 2134–2141, 1993.
122. Position of the American Dietetic Association. Nutrition Intervention in the treatment of anorexia nervosa, bulimia nervosa, and binge eating. J. Am. Diet Assoc. 94: 902–907, 1994.
123. Position of the American Dietetic Association and the Canadian Dietetic Association: Nutrition for physical fitness and athletic performance for adults. J. Am. Diet Assoc.
124. Position of the American Dietetic Association: vegetarian diets. J. Am. Diet Assoc.
125. Rosenbloom CA (ed). Sports Nutrition: A Guide for the Professional Working with Active People
. Chicago, IL: Am. Diatetic Association; 2000.
126. Rosenbloom, C., J. Storlie. A nutritionist’s guide to evaluating ergogenic aids. Am. Dietetic Assoc. SCAN’S Pulse. 17: 1–5, 1998.
127. Roy, B. D., M. A. Tarnopolsky. Influence of differing macronutrient intakes on muscle glycogen resynthesis after resistance exercise. J. Appl. Physiol. 84: 890–896, 1998.
128. Roy, B. D., M. A. Tarnopolsky, J. D. MacDougall, J. Fowles, K. E. Yarasheski. Effect of glucose supplement timing on protein metabolism after resistance training. J. Appl. Physiol. 82: 1882–1888. 1997.
129. Sampson DA. Vitamin B6. In. Wolinsky I, Driskell JA, eds. Sports Nutrition: Vitamins and Trace Elements
. Boca Raton, Fla: CRC Press 75–84:1997.
130. Sardinha, L. B., T. G. Lohman, P. J. Teixeira, D. P. Guedes, S. B. Going. Comparison of air displacement plethysmography with dual-energy X-ray absorptiometry and 3 field methods for estimating body composition in middle-aged men. Am. J. Clin. Nutr. 68: 786–793, 1998.
131. Sarubin A. The Health Professional’s Guide to Popular Dietary Supplements
. Chicago, IL: Am. Dietetic Association; 2000.
132. Schabort, E. J., A. N. Bosch, S. M. Weltan, T. D. Noakes. The effect of a preexercise meal on time to fatigue during prolonged cycling exercise. Med. Sci. Sports Exerc. 31: 464–471, 1999.
133. Sherman, W. M., G. Brodowicz, D. A. Wright, W. K. Allen, J. Simonsen, A. DernbackA. Effect of 4 h pre-exercise carbohydrate feedings on cycling performance. Med. Sci. Sports Exerc. 21: 598–604, 1989.
134. Shirreffs, S. M., A. J. Taylor, J. B. Leiper, R. J. Maughan. Post-exercise rehydration in man: Effects of volume consumed and drink sodium content. Med. Sci. Sports Exerc. 28: 1260–1271, 1996.
135. Sinning WE. Body composition in athletes. In: Roche AF, Heymsfield SB, Lohman TG, eds. Human Body Composition. Champaign, Ill: Human Kinetics Publishers; 257–273, 1996.
136. Speedy, D. B., T. D. Noakes, I. R. Rogers, J. M. D. Thompson, R. G. D. Campbell, J. A. Kuttner, D. B. Boswell, S. Wright, M. Hamlin. Hyponatremia in ultradistance triathletes. Med. Sci. Sports Exerc. 31: 809–815, 1999.
137. Sugiura, K., K. Kobayashi. Effect of carbohydrate ingestion on sprint performance following continuous and intermittent exercise. Med. Sci. Sports Exerc. 30: 1624–1630, 1998.
138. Sundgot-Borgen J. Eating Disorders. In: Berning JR, Steen SN, eds. Nutrition for Sport and Exercise
. Gaithersburg, Md: Aspen Publishers; 1998:pp.187–203.
139. Swinburn, B., E. Ravussin. Energy balance or fat balance? Am. J. Clin. Nutr. 57 (suppl): 766S-771S, 1993.
140. Tarnopolsky, M. A., S. A. Atkinson, J. D. MacDougall, A. Chesley, S. M. Phillips, H. Schwarcz. Evaluation of protein requirements for trained strength athletes. J. Appl. Physiol. 73: 1986–1995, 1992.
141. Thompson, J. L., M. M. Manore. Body weight regulation and energy needs: weight loss. In: Driskell JA, Wolinsky I, eds. Energy-Yielding Macronutrients and Energy Metabolism in Sports Nutrition
. Boca Raton, La: CRC Press; 2000, pp. 291–308.
142. Thompson, R. A., R. T. Sherman. Helping Athletes with Eating Disorders. Champaign, Ill: Human Kinetics Publishers; 1993.
143. Van Hall, G., J. S. H. Raaymakers, W. H. M. Saris, A. J. M. Wagenmakers. Ingestion of branched-chain amino acids and tryptophan during sustained exercise in man: failure to affect performance. J. Physiol. 486: 789–794, 1995.
144. Vozenilek G. The wheat from the chaff: Sorting out nutrition information on the internet. J. Am. Diet Assoc. 98: 1270–1272, 1998.
145. Vrigens, D. M. G., N. J. Rehrer. Sodium-free fluid ingestion decreases plasma sodium during exercise in the heat. J Appl Physiol. 86: 1847–1851, 1999.
146. Walsh, R. M., T. D. Noakes, J. A. Hawley, S. C. Dennis. Impaired high-intensity cycling performance time at low levels of dehydration. Int. J. Sports Med. 15: 392–398, 1994.
147. Webster, B. L., S. I. Barr. Body composition analysis of female adolescent athletes: comparing six regression equations. Med. Sci. Sports Exerc. 25: 648–653, 1993.
148. Wee, S-L., C. Willliams, S. Gray, J. Horabin. Influence of high and low glycemic index meals on endurance running capacity. Med. Sci. Sports Exerc. 31: 393–399, 1999.
149. Williams MH. The Ergogenic Edge. Pushing the Limits of Sports Performance. Champaign, Ill: Human Kinetics; 1998.
150. Williams MH. The use of nutritional ergogenic aids in sports: Is it an ethical issue? Int. J. Sport Nutr. 4: 120–131, 1994.
151. Williams, M. H., J. D. Branch. Creatine supplementation and exercise performance: An update. J. Am. Coll Nutr. 17: 216–234, 1998.
152. Wright, D. A., W. M. Sherman, A. R. Dernback. Carbohydrate feedings before, during or in combination improve cycling endurance performance. J. Appl. Physiol. 71: 1082–1088, 1991.
153. Young, V. R., P. L. Pellett. Plant protein in relation to human proteins and amino acid nutrition. Am. J. Clin. Nutr. 59 (suppl): 1203S-212S, 1994.
154. Zawadski, K. M., B. B. Yaspelkis, J. L. Ivy. Carbohydrate-protein complex increases the rate of muscle glycogen storage after exercise. J. Appl. Physiol. 72: 1854–1859, 1992.