14 research outputs found

    Sport Nutrigenomics: Personalized Nutrition for Athletic Performance

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    An individual's dietary and supplement strategies can influence markedly their physical performance. Personalized nutrition in athletic populations aims to optimize health, body composition, and exercise performance by targeting dietary recommendations to an individual's genetic profile. Sport dietitians and nutritionists have long been adept at placing additional scrutiny on the one-size-fits-all general population dietary guidelines to accommodate various sporting populations. However, generic “one-size-fits-all” recommendations still remain. Genetic differences are known to impact absorption, metabolism, uptake, utilization and excretion of nutrients and food bioactives, which ultimately affects a number of metabolic pathways. Nutrigenomics and nutrigenetics are experimental approaches that use genomic information and genetic testing technologies to examine the role of individual genetic differences in modifying an athlete's response to nutrients and other food components. Although there have been few randomized, controlled trials examining the effects of genetic variation on performance in response to an ergogenic aid, there is a growing foundation of research linking gene-diet interactions on biomarkers of nutritional status, which impact exercise and sport performance. This foundation forms the basis from which the field of sport nutrigenomics continues to develop. We review the science of genetic modifiers of various dietary factors that impact an athlete's nutritional status, body composition and, ultimately athletic performance

    International society of sports nutrition position stand: caffeine and exercise performance

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    Following critical evaluation of the available literature to date, The International Society of Sports Nutrition (ISSN) position regarding caffeine intake is as follows: 1. Supplementation with caffeine has been shown to acutely enhance various aspects of exercise performance in many but not all studies. Small to moderate benefits of caffeine use include, but are not limited to: muscular endurance, movement velocity and muscular strength, sprinting, jumping, and throwing performance, as well as a wide range of aerobic and anaerobic sport-specific actions. 2. Aerobic endurance appears to be the form of exercise with the most consistent moderate-to-large benefits from caffeine use, although the magnitude of its effects differs between individuals. 3. Caffeine has consistently been shown to improve exercise performance when consumed in doses of 3–6 mg/ kg body mass. Minimal effective doses of caffeine currently remain unclear but they may be as low as 2 mg/kg body mass. Very high doses of caffeine (e.g. 9 mg/kg) are associated with a high incidence of side-effects and do not seem to be required to elicit an ergogenic effect. 4. The most commonly used timing of caffeine supplementation is 60 min pre-exercise. Optimal timing of caffeine ingestion likely depends on the source of caffeine. For example, as compared to caffeine capsules, caffeine chewing gums may require a shorter waiting time from consumption to the start of the exercise session. 5. Caffeine appears to improve physical performance in both trained and untrained individuals. 6. Inter-individual differences in sport and exercise performance as well as adverse effects on sleep or feelings of anxiety following caffeine ingestion may be attributed to genetic variation associated with caffeine metabolism, and physical and psychological response. Other factors such as habitual caffeine intake also may play a role in between-individual response variation. 7. Caffeine has been shown to be ergogenic for cognitive function, including attention and vigilance, in most individuals. 8. Caffeine may improve cognitive and physical performance in some individuals under conditions of sleep deprivation. 9. The use of caffeine in conjunction with endurance exercise in the heat and at altitude is well supported when dosages range from 3 to 6 mg/kg and 4–6 mg/kg, respectively. 10. Alternative sources of caffeine such as caffeinated chewing gum, mouth rinses, energy gels and chews have been shown to improve performance, primarily in aerobic exercise. 11. Energy drinks and pre-workout supplements containing caffeine have been demonstrated to enhance both anaerobic and aerobic performance

    High levels of cognitive dietary restraint are associated with stress fractures in women runners

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    Societal emphasis on body image and the 'ideal' body weight drives many women to make conscious efforts to limit their food intake in order to achieve or maintain a desired body weight. This attitude and eating behaviour is characterized by a preoccupation with food-related issues, and is referred to as dietary restraint or cognitive dietary restraint (CDR). The most commonly used instrument to measure and assess this dietary restraint is the restraint scale of the Three-Factor Eating Questionnaire (TFEQ). Female athletes are faced with body image challenges, as well as trying to achieve a body weight that is optimal for their performance. Many female athletes could therefore be experiencing these restrained eating patterns, to meet the combined pressures of an 'ideal body1 and enhanced performance. Most previous studies have generally found similar physical characteristics and energy intakes among women with differing restraint scores. However, CDR has been associated with subclinical menstrual cycle irregularities (MCI) and increased Cortisol levels, both of which can affect bone mineral density (BMD). Preliminary evidence has also reported an association between CDR and BMD or bone mineral content (BMC). Low BMD has been implicated in stress fracture risk, and runners are particularly at risk for lower extremity stress fractures. The purpose of this investigation was to assess CDR in female runners with a recent stress fracture (SF) and without a history of stress fracture (NSF). We recruited nulliparous normal-weight runners (running >20 km/wk) who were non-smokers, had regular menstrual cycles, were not currently dieting and had no history of an eating disorder. A sample of 79 runners (n = 38 SF, 29±5 yr; n = 41 NSF, 29±6 yr) completed a 3-day food record and questionnaire assessing physical activity, menstrual cycle history and perceived stress. The TFEQ was used to assess eating attitudes and behaviours, including CDR. SF and NSF runners had similar body mass index (21.2±1.8 vs 22.0±2.5 kg/m²), physical activity (35.7±13.5 vs 33.4±1.34 km/wk), perceived stress, and energy and macronutrient intakes. However, CDR was significantly higher in SF runners (11±5.4 vs 8.4±4.3, p<0.05). We conclude that women runners with a history of recent SF have higher levels of CDR. Subclinical MCI and increased Cortisol levels associated with high CDR may contribute to lowered BMD and increased risk for stress fracture. Prospective studies that include measurements of menstrual cycle characteristics, Cortisol levels and BMD are needed to determine if CDR is an independent risk factor for stress fractures, mediated by subclinical MCI and elevated Cortisol with subsequent bone loss.Land and Food Systems, Faculty ofGraduat

    Genetic Modifiers of Caffeine and Endurance Performance in Athletes

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    Background: Caffeine is used as an ergogenic aid by athletes to improve performance. However, the effects of caffeine differ between athletes. This may be due to genetic differences affecting caffeine metabolism and caffeine response during exercise. Objective: The aim was to determine whether variation in the CYP1A2 gene, which affects caffeine metabolism, and the HTR2A gene, which encodes serotonin receptors and may affect caffeine response, modify the ergogenic effects of caffeine during a 10-km cycling time trial. Methods: Competitive male athletes (n=101; age: 25 ± 4 years) completed the time trial under three conditions: 0, 2 or 4 mg of caffeine per kg body mass, using a split-plot randomized, double-blinded, placebo-controlled design. DNA was isolated from saliva and genotyped for polymorphisms in CYP1A2 (rs762551) and HTR2A (rs6313). Results: Overall, 4 mg/kg caffeine decreased cycling time by 3% versus placebo. A significant (pPh.D

    Genetic Modifiers of Caffeine and Endurance Performance in Athletes

    No full text
    Background: Caffeine is used as an ergogenic aid by athletes to improve performance. However, the effects of caffeine differ between athletes. This may be due to genetic differences affecting caffeine metabolism and caffeine response during exercise. Objective: The aim was to determine whether variation in the CYP1A2 gene, which affects caffeine metabolism, and the HTR2A gene, which encodes serotonin receptors and may affect caffeine response, modify the ergogenic effects of caffeine during a 10-km cycling time trial. Methods: Competitive male athletes (n=101; age: 25 ± 4 years) completed the time trial under three conditions: 0, 2 or 4 mg of caffeine per kg body mass, using a split-plot randomized, double-blinded, placebo-controlled design. DNA was isolated from saliva and genotyped for polymorphisms in CYP1A2 (rs762551) and HTR2A (rs6313). Results: Overall, 4 mg/kg caffeine decreased cycling time by 3% versus placebo. A significant (pPh.D

    Cognitive dietary restraint is associated with stress fractures in women runners.

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    High levels of cognitive dietary restraint (CDR) have been associated with subclinical menstrual cycle irregularities and increased cortisol levels, both of which can affect bone mineral density (BMD). Low BMD has been implicated in stress fracture risk. We assessed CDR in female runners (≥ 20 km/wk) with a recent stress fracture (SF) and with no stress fracture history (NSF). A sample of 79 runners (n = 38 SF, 29 ± 5 y; n = 41 NSF, 29 ± 6 y) completed a 3-d food record and questionnaire assessing physical activity, menstrual cycle history, and perceived stress. SF and NSF runners had similar body mass index (21.2 ± 1.8 vs. 22.0 ± 2.5 kg/m2), physical activity (35.7 ± 13.5 vs. 33.4 ± 1.34 km/wk), perceived stress, and dietary intakes. CDR, however, was higher in SF runners (11.0 ± 5.4 vs. 8.4 ± 4.3, P &lt; 0.05). Subclinical menstrual cycle disturbances and increased cortisol levels that are associated with high CDR, might in turn contribute to lowered BMD and increased stress fracture risk.</jats:p

    Caffeine, CYP1A2 Genotype, and Endurance Performance in Athletes

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