Switching from Gluten-Free to Low FODMAP Diet to Reduce Digestive Problems in Athletes

Various nutrition strategies have been implemented with the aim to reduce exercise-associated GIS in training and competition [11–14]. Pre-exercise diet recommendations to attenuate symptoms during exercise include reduced fiber/low residue, low fat, moderate protein, and avoidance of lactose-containing dairy products. The transient nature and difficulty in reproducing GIS present a challenge in determining the efficacy of these strategies. Consequently, athletes pursue a variety of dietary approaches aimed at reducing GIS. Anecdotal-based approaches or implementation of strategies ad hoc abound, but several evidence-based strategies for reducing GIS have been established [11–14]. One example is ingesting multiple transporter carbohydrates (e.g. glucose and fructose blends) during exercise [15]. More recently, an investigation in runners (six males, five females) demonstrated that carbohydrate and protein intake during exercise under conditions of heat stress (2 h run at 60% maximal oxygen uptake in a 35 °C environment) ameliorated intestinal injury and permeability and decreased GIS with the carbohydrate feeding intervention [16]. Gut training to increase carbohydrate tolerance and prepare race-day nutrition has also been shown to be beneficial [11, 17, 18]. Mechanisms potentiating nutrient malabsorption, such as intestinal injury or decreased intestinal transporter activity, require further consideration when implementing strategies to address exercise-induced gastrointestinal syndrome [19]. Symptoms often persist despite implementation of a variety of strategies.

Being the body’s largest immune organ, the gut is central to immune function, which is further influenced by dietary intake and exercise [20, 21]. It is plausible that stress placed on the gut occurring more frequently than the 3–5 days required for epithelial cell protein turnover [22] generates a state with various levels of perpetual intestinal injury. This circumstance may increase susceptibility to dietary triggers (e.g. gluten) or food intolerances (e.g. lactose), associated GIS, and the long-term development of chronic disease [1]. Although this concept has not been directly demonstrated in athletes, better understanding of dietary factors affecting GIS [e.g. fermentable oligo-, di-, monosaccharides and polyols (FODMAPs)] has improved the practitioner’s toolbox for symptom management [23]. Bridging clinical and sports nutrition will become increasingly fundamental for the efficacious management of exercise-induced gastrointestinal syndrome and gastrointestinal conditions in athletes.

There are two main aims for this review. The first aim is to provide the sports nutrition practitioner with an overview of the current state of knowledge and considerations pertaining to the appropriateness of a gluten-free diet (GFD) for athletes without a clinical requirement for this diet. The second aim is to review the use of FODMAP restriction in clinically healthy athletes to decrease GIS.

A high number of athletes link exercise-associated GIS with dietary triggers, particularly gluten-containing foods [14]. As a result, foods or food groups are eliminated from the diet, potentially unnecessarily. Gluten-containing foods are commonly blamed for GIS. Gluten, a plant storage protein, is a composite of gliadins and glutenins, complex proteins unusually rich in prolines and glutamines that are incompletely digested by intestinal enzymes [24]. It is also important to acknowledge that gluten and fructans co-exist in cereals and yet gluten has been incorrectly blamed for related GIS [25–27]. In celiac disease, partial peptide digestion triggers increased intestinal permeability and innate and/or adaptive immune responses resembling exposure to gastrointestinal pathogens [28]. Non-celiac gluten/wheat sensitivity (NCGS) is acknowledged as a separate clinical entity, with symptoms similar to celiac disease. NCGS is characterized by variable pathogenesis, clinical history, and clinical course [29]. In other words, it is a heterogeneous condition but has symptom overlap with other conditions, such as irritable bowel syndrome (IBS). Advancing work is narrowing the clinical picture for NCGS and suggests a central role of the intestinal innate immune system and elevated levels of intestinal fatty acid binding protein [30, 31]. However, due to the lack of a diagnostic biomarker for NCGS, non-specific symptoms, as well as the resemblance to gastrointestinal and extraintestinal symptoms associated with strenuous exercise (e.g. fatigue, bloating, diarrhea), many athletes believe gluten to be the cause.

A recent questionnaire-based study quantified athletes’ (n = 910) beliefs and reasons for adhering to a GFD [14]. Forty-one percent of the non-celiac athletes surveyed reported following this diet [14, 32] at least 50% of the time [14]. The foremost rationale for athletes to adhere to a GFD was self-diagnosis of gluten-related conditions or non-clinical motivations (e.g. healthier, improved body composition) [14]. Observationally, athletes often implement dietary strategies ahead of supportive research, which may or may not be accurate. It is however prudent to consider a potential interplay between exercise-induced gastrointestinal injury, gastrointestinal dysfunction, and susceptibility to the negative effects of known dietary triggers, in this case gluten.

Average intakes of gluten vary individually and geographically [33]. Athletes’ consumption of gluten-containing foods may be higher than average due to the increased volume of food and possibly higher reliance on wheat-based foodstuff (e.g. energy bars, breads, and pasta) to fuel elevated energy and carbohydrate demands. The combination of increased exercise-induced gastrointestinal permeability and high intakes of gluten peptides could allow for a greater gliadin peptide translocation across the epithelial barrier. This permutation of physiological stress and consumption of a known dietary trigger could amplify GIS associated with exercise-induced gastrointestinal syndrome. In vivo, this concept is speculative, and current research is limited to cell culture studies or populations with celiac disease that have demonstrated that gliadin peptides trigger, or are associated with, tight junction protein dysregulation [34, 35]. In the only randomized controlled trial to investigate athletes’ (n = 13) gastrointestinal injury and symptoms in response to a GFD during strenuous exercise, gluten did not increase exercise-induced alterations in epithelial injury or GIS [36]. While the alleged detrimental effects of gluten on gut barrier function or GIS in healthy athletes have not been validated, a multitude of physiological elements and psychosocial factors influence GIS and the perception of gluten’s effect on gastrointestinal health.

In addition to exercise stress, the potential of gluten to trigger inflammatory responses could have an additive toll on the immune system [1]. Immune-associated symptoms are difficult to isolate, yet the influential role of nutrition on immune parameters is an integral component of athletic health and performance. A ‘J-shaped curve’ model has been used to demonstrate the relationship between high-volume/intensity exercise and increased illness rate [37]. In celiac disease, a GFD restores innate and adaptive immune parameters [38]. However, no evidence supports the idea that gluten avoidance in clinically healthy athletes improves measures of immune function [36, 39]. In a 7-day randomized crossover GFD intervention study of competitive non-celiac cyclists (n = 13), gluten did not elicit an adverse inflammatory profile (interleukin (IL)-1β, IL-6, IL-8, IL-10, IL-15, tumor necrosis factor-α) pre, during, or after a strenuous cycling bout (45-min steady-state cycling at 80% maximum power at VO_2max, followed by a 15-min time trial) compared with an isocaloric gluten-containing diet [36]. Nutrition strategies that improve immune function are desirable, particularly during heavy training periods. However, too little is known about the effect of gluten on immune health to support adherence to a GFD for clinically healthy athletes. Future work should continue to evaluate the unique connection between a GFD and the body’s cornerstone for immune health, the gut [14].

Perceptions of improved perceptual wellbeing [14] are likely influenced by dietary changes concurrent with following a special diet, and not gluten itself. Following a GFD may increase awareness of food choices and encourage more fruit, vegetable, and gluten-free whole-grain intake [14]. These are healthy eating guidelines that align with foundational sports nutrition recommendations [40]. Positive dietary changes associated with this diet are likely to influence perceptions of improved health, psychology, or exercise performance. The ‘belief effect’ is also expected to influence performance outcomes [41] as many athletes trust that a GFD provides an ergogenic edge [14, 32] and has a net positive impact on performance outcomes [41]. However, when 13 trained cyclists were blinded, no difference in a 15-min time-trial performance was found between a gluten-containing diet (245.4 ± 53.4 kJ) and a GFD (245.0 ± 54.6 kJ) [36]. Widespread convictions of the overall health and performance benefits of a GFD are not well-supported in athletes not requiring gluten avoidance. In a few cases, the ‘belief effect’ as it relates to a GFD may be a strategic ergogenic tool; however, these circumstances should be carefully assessed.

In many endurance and aesthetic sports, body composition is an important factor in performance outcomes. Weight changes before and after adherence to a GFD have been examined in celiac disease. However, poor dietary control, methodological differences, and a complexity of confounding factors (e.g. type 1 diabetes) limit the applicability of findings to healthy athletes without celiac disease [42, 43]. A possible increased risk of obesity with adherence to a GFD in celiac disease populations is suggested to be linked to improved nutrient absorption upon villus recovery. Intakes of gluten-free specialty products, historically higher in fat and sugar than their gluten-continuing counterparts, may also contribute to increased obesity [43]. Research in male mice suggests some metabolic differences pertaining to adiposity and metabolism with a GFD versus an isocaloric gluten-containing diet over 8 weeks [44, 45]. Impaired glucose homeostasis, decreased fasted and non-fasted oxygen uptake, lowered energy expenditure, and increased adipocyte content and proinflammatory cytokines were associated with increased body weight and adipose tissue in gluten-fed mice [45]. Upregulated expression of some genes (e.g. peroxisome proliferator-activated receptor-α and -γ, lipoprotein lipase) and hormone concentrations (e.g. leptin, resistin) provide some mechanistic insight [45]. Although these in vitro findings provide an interesting rationale, it would be far-reaching to accept that gluten would elicit the same alterations in clinically healthy athletes. Dietary changes and confounding factors associated with a GFD may be more potent influencers of energy balance and body composition.

Only approximately 1% of Americans have diagnosed celiac disease [46]. According to the National Health and Nutrition Examination Survey (2009–2014; n = 7417), 25% of American consumers reported consuming gluten-free foods in 2015, representing a 67% increase from 2013 [46, 47]. GFD adherence in athletes is estimated to be fourfold higher than the proportion of the general population that is considered to require gluten-avoidance for clinical reasons (e.g. celiac disease, wheat allergy, NCGS) [14]. As mentioned, positive dietary behaviors may accompany a GFD. However, unnecessary food restriction is concerning for athletes given increased fuel requirements and the importance of adequate nutrient intake on health, training adaptation, and performance [14, 40, 48]. Elimination-type diets pose a risk of suboptimal fueling and uncertainty remains whether a GFD is a healthier or less healthy diet to support athlete nutrition demands [49]. Previous studies have found no difference in energy intake with a GFD compared with control diets. However, suboptimal intake of fiber, vitamin D, vitamin B12, folate, iron, zinc, magnesium, and calcium have been reported [42, 50]. With one-quarter of Americans eating gluten-free foods, it is also speculated that consuming alternative rice-based grains may increase exposure to higher levels of arsenic and mercury [47]. In many parts of the world, a proliferating gluten-free market has improved the availability of more nutrient-rich pseudo-cereal-based products, such as amaranth, buckwheat, and quinoa. These are replacing less nutritious corn and rice flour and reducing suboptimal nutrient concerns [51]. However, athletes with modest nutrition knowledge, limited capacity to finance more expensive gluten-free food products [48], or travelling abroad for training/competition may still face food accessibility challenges. Alongside unique athletic fueling requirements, the socioeconomical, psychological, and logistical implications associated with a GFD should be considered when determining the appropriateness of the worlds most popular diet for athletes [52, 53]. An individualized and evidence-based approach to a GFD is advised to optimize nutrition intake to support optimal wellbeing, training adaptation, and performance.

An emerging trend of athletes self-diagnosing NCGS has been partially underpinned by the lack of a definitive diagnostic biomarker [52, 57, 58]. As mentioned, advancing work proposes that a unique systemic immune response to microbial and wheat antigens, together with intestinal cell damage, occurs in NCGS [59]. Until validation of established biomarkers becomes possible, athletes may continue to attribute gastrointestinal issues to gluten. However, other proteins or nutrients existing in wheat-based foods could be the actual culprits. A previous review has extensively summarized the potential for other proteins existing in gluten-containing grains, mainly cereal protein amylase-trypsin inhibitors, to trigger GIS [60]. Amassing evidence indicating that FODMAPs play a role in augmenting exercise-induced GIS suggests that this frontline dietary management for IBS may cross over to address GIS in athletes [1, 13, 61, 62]. Certain FODMAPS are subsequently reduced with the reduction of wheat-based grains. A decrease in FODMAP intake and not gluten itself may be the true factor for improved GIS attributed to a GFD [63]. This has been well-demonstrated in a handful of clinical studies indicating that fructan and not gluten elimination reduced GIS in IBS patients with self-reported NCGS [26, 63, 64]. This promising area of work may open an entirely novel dietary strategy to manage an extremely common illness among athletes.

A recent questionnaire-based study reported that 55% of athletes (n = 910) self-report eliminating at least one food high in FODMAPs with the aim to reduce GIS [13]. Subsequently, up to 85% reported symptom improvement with removal of the offending food. Lactose (86.5%) was most frequently eliminated, followed by GOS (23.9%), fructose (23.0%), fructans (6.2%), and polyols (5.4%). A case study report of a clinically healthy competitive multisport athlete with persistent exercise-induced GIS similarly confirmed FODMAP restriction compared with a high FODMAP diet (7.2 ± 5.7 g vs. 81.0 ± 5.0 g·FODMAP·day⁻¹) measurably reduced daily and during exercise GIS. Lactose intake was presumably the most ubiquitous symptom contributor [61]. Correspondingly, athletes with IBS, estimated to account for 22% of endurance athletes [72], would likely benefit from FODMAP restriction, both for daily and sport-specific fueling.

The efficacy of FODMAP modification for the treatment of exercise-induced GIS in clinically healthy endurance athletes is emerging as a novel approach to attenuate symptoms [1, 73]. The physiological alterations occurring with exercise-induced gastrointestinal syndrome may impair nutrient absorption, alter gastric/intestinal motility, and impair overall gastrointestinal function. Impaired digestion and absorption of FODMAPs may contribute to symptoms related to this multifactorial condition. Adverse lower GIS appear to be dominant in exercise and may be associated with the osmotic effect of these malabsorbed carbohydrates, which can increase luminal water content first in the small intestine [74]. Undigested FODMAPs then travel to the ileum and onwards, where rapid bacterial fermentation may increase intestinal luminal pressure by increasing colonic content through gas production (e.g. H₂, CH₄, CO₂, and H₂S) and osmotic water translocation. Subsequently, lower GIS are triggered or amplified [75, 76]. As a result, bloating, abdominal pain, flatulence and alterations in bowel movement may occur with greater severity in hypersensitive individuals [70, 75]. FODMAPs also influence upper GIS, such as the sensation of fullness, as demonstrated in a clinical feeding study that administered doses of fructose and glucose via gastric infusion [77]. FODMAPs are not likely to be an exclusive GIS trigger but may amplify symptoms initiated by other factors [1, 62].

IBS-like symptoms experienced by many athletes are likely induced by the mechanical, psychological, environmental, and nutritional components related to strenuous exercise. Several dietary strategies may decrease the magnitude of these symptoms. Recently, a short-term low FODMAP diet has been shown to significantly reduce daily GIS in clinically healthy runners with exercise-associated GIS [62]. This randomized, blinded, crossover study assessed the efficacy of a short-term low FODMAP diet (6 days in total), including 2 days of prescribed high-intensity running, on daily and during exercise GIS compared with a high FODMAP diet. A significantly smaller area under the curve for daily GIS was demonstrated in 80% of subjects with consumption of a low compared with a high FODMAP diet [62]. During exercise in the two conditions, symptoms were not significantly different and it is probable that an exercise bout of longer duration or greater intensity may be required to detect measurable differences in GIS during exercise between the two diets [e.g. 2 h running at 60% maximal oxygen uptake (VO_2max)]. Results from this study verify previous case study outcomes and establish the foundation for future research [61]. Forthcoming investigations of the efficacy of FODMAP modification in athletic populations should aim to determine the ideal timing and amount of FODMAP intake around strenuous exercise while maintaining a focus on minimizing the risks associated with unnecessary food restriction.

A small number of studies have used breath testing to measure carbohydrate malabsorption during and post exercise, with variable results [11, 79, 80]. During mixed endurance exercise (3 h at 75% VO_2max), breath hydrogen was higher during running than during cycling, with ingestion of glucose-rich carbohydrates in semi-solid and fluid forms (approximately 1.2 g·kg body mass·h⁻¹), resulting in negligibly higher breath hydrogen excretion (2–3 ppm increase) compared with a non-carbohydrate placebo [79]. It is likely that increased ventilation rates accompanying exercise may skew gas (hydrogen) production values, and the ecological significance is unspecified. Measures taken during the recovery time course after exercise may be more accurate. In a gut adaptability study, after 3 h of running (2 h at 60% VO_2max, followed by a 1 h distance test), 68% of runners demonstrated evidence of carbohydrate malabsorption (breath hydrogen ≥ 10 ppm above baseline) during the recovery period [11]. Forthcoming research will better characterize FODMAP malabsorption during and after exercise to better inform food selection. However, hydrogen breath testing has demonstrated poor reproducibility and low predictive value for symptom responses to lactose and fructose [78]. Variable absorption of FODMAPs should be considered a potential factor contributing to GIS, but the use of breath testing to diagnose malabsorption may not be reliable [78].

Depending on the extensiveness of high FODMAP food restriction, several complications associated with a strict long-term low FODMAP diet have been identified. A low FODMAP diet may be associated with alterations in gut microbiota, reduced short-chain fatty acid production, and impacts on aspects of physical and psychological wellbeing, similar to those mentioned in Sect. 2.5 with regard to a GFD [75, 76, 81]. Diminished concentrations of bifidobacteria after 3–4 weeks of reduced FODMAP intake have been observed [76, 81]. Exercise may neutralize the adverse effects of diminished prebiotic consumption on the microbiota. If adherence to FODMAP restriction is periodic/short-term, or limited to a few foods, altered microbiota is less concerning [82]. Coadministration of a multistrain probiotic has also been shown to mitigate the detrimental effects of lowered prebiotic intake [83, 84]. In addition, short-chain fatty acid production, which is highly reliant on fermentation of undigested carbohydrates in the large intestine [85, 86], may theoretically be compromised with reduced substrate. However, after 21 days of a low FODMAP diet, short-chain fatty acid fecal concentrations were similar between the low FODMAP and control diets [81]. A multitude of dietary and environmental factors modulate the composition and metabolic activity of the gut microbiota. Research on the microbiota in clinically healthy athletes implementing a low FODMAP diet has not been published; however, it is prudent to consider this aspect of gut health with frequent or long-term FODMAP restriction.

FODMAP diet application in the athletic arena is in its infancy; however, the development of low FODMAP sports food products/energy bars, as well as oral nutrition supplements [89], will support adherence to sports nutrition guidelines alongside FODMAP restriction. Introduction of a low FODMAP diet must be carefully navigated to minimize the risks associated with unnecessary dietary restriction (Fig. 2) [75, 90, 91]. It is imperative that practitioners consider underlying clinical conditions, such as functional gastrointestinal disorders (e.g. IBS, Crohn’s disease, functional idiopathic nausea), and the potential for unnecessary food restriction to foster eating disorders.