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Review

The Low FODMAP Diet: Many Question Marks for a Catchy Acronym

Department of Pediatrics, Università Politecnica delle Marche, Via F. Corridoni 11, 60123 Ancona, Italy
*
Author to whom correspondence should be addressed.
Nutrients 2017, 9(3), 292; https://doi.org/10.3390/nu9030292
Submission received: 29 December 2016 / Revised: 6 March 2017 / Accepted: 13 March 2017 / Published: 16 March 2017

Abstract

:
FODMAP, “Fermentable Oligo-, Di- and Mono-saccharides And Polyols”, is a heterogeneous group of highly fermentable but poorly absorbed short-chain carbohydrates and polyols. Dietary FODMAPs might exacerbate intestinal symptoms by increasing small intestinal water volume, colonic gas production, and intestinal motility. In recent years the low-FODMAP diet for treatment of irritable bowel syndrome (IBS) has gained increasing popularity. In the present review we aim to summarize the physiological, clinical, and nutritional issues, suggesting caution in the prolonged use of this dietary treatment on the basis of the existing literature. The criteria for inclusion in the FODMAPs list are not fully defined. Although the low-FODMAP diet can have a positive impact on the symptoms of IBS, particularly bloating and diarrhea, the quality of the evidence is lower than optimal, due to frequent methodological flaws, particularly lack of a proper control group and/or lack of blinding. In particular, it remains to be proven whether this regimen is superior to conventional IBS diets. The drastic reduction of FODMAP intake has physiological consequences, e.g., on the intestinal microbiome and colonocyte metabolism, which are still poorly understood. A low-FODMAP diet imposes an important restriction of dietary choices due to the elimination of some staple foods, such as wheat derivatives, lactose-containing dairy products, many vegetables and pulses, and several types of fruits. For this reason, patients may be at risk of reduced intake of fiber, calcium, iron, zinc, folate, B and D vitamins, and natural antioxidants. The nutritional risk of the low-FODMAP diet may be higher in persons with limited access to the expensive, alternative dietary items included in the low-FODMAP diet.

1. Introduction

FODMAP, “Fermentable Oligo-, Di- and Mono-saccharides And Polyols”, is a heterogeneous group of highly fermentable but poorly absorbed short-chain carbohydrates and polyols. The acronym FODMAP was first coined in 2005 by Gibson and Shepherd at Monash University in Melbourne, Australia, in a personal view article suggesting a link between the western lifestyle, the intake of FODMAP-rich foods, and susceptibility to Crohn's disease [1]. Soon after, the Australian group focused on the use of a low-FODMAP diet in the treatment of irritable bowel syndrome (IBS) [2], and in one of their most influential papers they showed that symptom improvement in patients with IBS and suspected non-celiac gluten sensitivity (NCGS) was not related to gluten avoidance, but to the concomitant reduction of FODMAP intake determined by the gluten-free diet (GFD). Interestingly, that study was double-blinded and placebo-controlled for the gluten challenge, but not for the reduction of dietary FODMAPs [3]. In recent years the putative role of FODMAPs in IBS has gained wide popularity in the general public and the subject has been addressed in books promoting the low-FODMAP diet and related recipes [4]. The recently revised British Dietetic Association (BDA) guidelines for the dietary management of IBS recommend the low-FODMAP diet as the second-line intervention in IBS patients [5]. A 2016 meta-analysis supports the efficacy of a low-FODMAP diet in the treatment of functional gastrointestinal symptoms [6]. Treatment with the low-FODMAP diet has also been advocated for diverticulitis [7], exercise-induced gastrointestinal symptoms [8], and inflammatory bowel diseases [9]. Although these studies indicate that a subgroup of patients with IBS may benefit from eating less highly fermentable sugars, i.e., the low-FODMAP diet [6], there are still several open questions regarding the physiology, the efficacy, and the safety of this dietary treatment.
In this paper the physiological, clinical, and nutritional issues suggesting caution in the prolonged use of the low-FODMAP diet will be summarized on the basis of the existing literature. The literature search was conducted in the PubMed MEDLINE and SCOPUS databases using the term “FODMAP” and “irritable bowel syndrome”, and only articles in English were extracted. We identified 98 papers, and selected 17 prospective, intervention trials for analysis.

2. What Is FODMAP?

FODMAP is not a single entity, but a group of compounds, including oligosaccharides (fructans, fructo-oligosaccharides = FOS and galacto-oligosaccharides = GOS), disaccharides (lactose), monosaccharides (fructose), and polyols (sorbitol, mannitol, maltitol, xylitol, polydextrose, and isomalt). The list of dietary sugar alcohols (polyols) includes tens of compounds used widely and unpredictably by the food industry as thickeners and sweeteners. Lactose belongs to FODMAPs only in individuals showing non-persistence of high lactase levels, which is a highly variable percentage of subjects in different populations. On the other hand, lactulose is an orally administered, non-absorbable disaccharide that is used in the treatment of constipation, a problem affecting many patients with IBS, and should definitely be avoided in subjects undergoing the FODMAP exclusion.
The FODMAP definition is based on functional instead of biochemical characteristics: being poorly absorbable and highly fermentable in the intestine is the common denominator of FODMAPs. They might exacerbate IBS symptoms through various mechanisms, such as increasing small intestinal water volume, colonic gas production, and intestinal motility. Conversely, FODMAPs have important physiological effects: they increase stool bulk, enhance calcium absorption and modulate immune function, and decrease the levels of serum cholesterol, triacylglycerols, and phospholipids. They selectively stimulate the growth of some microbial groups such as Bifidobacteria (prebiotic effect) [10]. Due to their capacity to stimulate the growth of nonpathogenic intestinal microflora, FOS and GOS are increasingly included in food products and infant formulas [11]. Fermentation of small, fermentable carbohydrates in the colon results in the production of short-chain fatty acids (SCFAs = acetate, propionate, and butyrate) that have a trophic effect on the colonocyte metabolism by increasing energy production and cell proliferation, and protecting against colon cancer [12,13]. All of the above positive effects are obviously lost with the low-FODMAP diet.
The boundaries of a low-FODMAP diet are not perfectly known. The appreciable work of the Melbourne group produced some analytical tables on the food content of specific FODMAPs [14,15,16], however, (a) many commercial items are missing in this list; and (b) the content of FODMAPs in vegetables is highly variable, e.g., according to the degree of maturation [17]. Furthermore, the possible interactions between FODMAPs and other nutrients are still unclear.
Finally, how much is a “normal” and how much is a low FODMAP intake? This has not yet been defined in quantitative terms.

3. Efficacy of the Low-FODMAP Diet: What Is the Quality of the Evidence?

Table 1 reports the clinical trials that are available in the literature on the effect of a low-FODMAP diet in IBS patients [3,18,19,20,21,22,23,24,25,26,27,28,29,30,31,32,33]. In general, most studies and one meta-analysis [6] have shown that IBS symptoms, particularly bloating and abdominal pain, may benefit from this treatment. However, the quality of the evidence is lower than optimal in our opinion, due to frequent methodological flaws, particularly a lack of a proper control group and/or lack of blinding, as shown in the last column of Table 1. The finding that the low-FODMAP diet improves IBS symptoms in comparison with a normal diet does not prove that this treatment is superior to the conventional IBS dietary intervention, e.g., the restriction of high-fiber food, resistant starch, fresh fruit, coffee, tea, alcohol, fizzy drinks and sorbitol, as recommended by the British National Institute for Health and Care Excellence (NICE) guidelines [34].
Indeed, studies comparing the efficacy of the low-FODMAP diet vs. proper dietary advice for IBS did not show a clear-cut advantage of the low-FODMAP diet: (a) in a US trial, 40%–50% of patients reported adequate relief of their IBS with diarrhea symptoms with the low-FODMAP diet or a diet based on modified NICE guidelines, even though the low-FODMAP diet led to significantly greater improvement in individual IBS symptoms, particularly pain and bloating, compared with the NICE diet [31]; (b) in a Swedish study the severity of IBS symptoms was reduced in both the low-FODMAP and the conventional IBS diet groups, at the end of a four-week period of treatment [26].
Due to the lack of a biomarker of “FODMAP intolerance”, the gold standard for proving the causal role of FODMAP, as well as other food intolerances/allergies, remains the double-blind placebo-controlled (DBPC) challenge. Three FODMAP challenge studies showed that high doses of fructose or fructans significantly worsen IBS symptoms [18,32,33]. Another randomized, DBPC study showed that gastrointestinal symptoms increased significantly after sorbitol and mannitol ingestion in patients with IBS compared to controls [14]. No DBPC challenge study is available for other FODMAPs or a mixed FODMAP-containing diet.
The duration of treatment with the low-FODMAP diet is rather short in the majority of published studies. This is a limitation for the evaluation of the low-FODMAP diet’s long-term efficacy. IBS is a chronic/recurrent condition but this treatment is difficult to maintain over time, due to many food exclusions. In a recent follow-up study of patients with IBS or inflammatory bowel disorder (IBD) treated with the low-FODMAPs diet, only one-third were still adherent to the diet after a median follow-up of 18 months [35]. The inventors of the low-FODMAP diet suggest an “all-FODMAP” free diet for two months followed by a serial challenge with one FODMAP per week (so called FODMAP reintroduction plan) [4]. Not only is the rationale of this challenge unclear, given that the physiological effects of FODMAP are not expected to change in such a short period of time, but also unpractical, since the list of food to reintroduce on a weekly basis is extremely long.

4. Is a Low-FODMAP Diet a Safe Approach?

The drastic reduction of FODMAP intake could have consequences that are still poorly understood on (a) the colonocyte metabolism (see Paragraph 2), (b) the intestinal microbiota, and (c) the nutritional status.
There is good evidence supporting the concept that the intestinal microbiota is perturbed in patients with IBS. Several recent studies have reported an increase in the relative abundance of Firmicutes, mainly Clostridium cluster XIVa, and Ruminococcaceae, together with a reduction in the relative abundance of Bifidobacteria. A lower diversity and a higher instability of the microbiota in IBS patients compared to controls have also been reported [36]. A low-FODMAP diet paradoxically does not correct these microbiota modifications, but induces similar changes, i.e., reducing the Bifidobacteria counts [20], and the total bacterial abundance [22], while increasing the abundance of Ruminococcacae [36]. This dietary treatment induces decreased levels of fecal Faecalibacterium prausnitzii and total SCFAs/n-butyric acid [33]. Extensive analyses of microbiota composition, functionality, and fermentation products in relation to symptom generation are currently lacking. Finally, the long-term effects of the microbiota changes induced by the low-FODMAP diet, if any, remain to be determined.
A low-FODMAP diet imposes an important restriction of dietary choices due to the elimination of some staple foods, such as wheat derivatives, lactose-containing dairy products, many vegetables and pulses, and several types of fruits (Table 2).
Despite the lack of studies on the long-term nutritional consequences of the low-FODMAP diet, possible risks of this treatment may be inferred from data available for other exclusion diets. As for cereal intake, the exclusion of wheat, rye, and barley is the same as the gluten-free diet (GFD) used for celiac disease treatment. Nutritional surveys have shown that subjects on a GFD may be at risk of reduced intake of fiber, calcium, iron, zinc, folate, and other B-group vitamins [37]. A deficient intake of dietary fiber may be expected to occur even more frequently on the low-FODMAP diet, due to a significant restriction of other fiber sources, such as fruit, vegetables, and legumes. The consequences of a fiber-poor diet may be particularly deleterious in subjects complaining of constipation as a manifestation of IBS. The restriction of lactose-containing dairy products may enhance the tendency to poor calcium availability since (a) these items are a primary source of calcium; and (b) the promoting effect of lactose on calcium absorption is lost [38,39]. A low-FODMAP diet may also be poor in natural antioxidants, such as flavonoids, carotenoids, and vitamin C contained in some FODMAP-rich vegetables (e.g., cauliflower, onion, garlic), or phenolic acid and anthocyanins present in fruits and blackberries. Wheat (which is excluded from the low-FODMAP diet) is a major source of phenolic acids, such as ferulic acid, caffeic acid, p-coumaric acid, p-hydroxybenzoic acid, vanillic acid, and protocatechuic acid [40]. Finally, the exclusion of dairy products in a low-FODMAP diet may favor a vitamin D deficiency [41].
We speculate that the nutritional risk of the low-FODMAP diet, in the long term, may follow an inverse socio-economic gradient, since persons with economical restraints may have limited access to many of the expensive, alternative dietary items included in the low-FODMAP diet (e.g., berries, exotic fruit, and pseudo-cereals).

5. Conclusions

The low-FODMAP diet can have a positive impact on the symptoms of IBS, particularly bloating and diarrhea. However, it remains to be proven whether this regimen is superior to conventional IBS diets. The drastic reduction of FODMAP intake could have physiological consequences on the colonocyte metabolism, the intestinal microbiota, and the nutritional status, which need further investigation. Based on our review, it might be helpful to consider the use of nutritional supplements to avoid possible deficiencies induced by a strict low-FODMAP diet over the long term.

Author Contributions

All authors conceived this work, G.C. performed the literature search and the data extraction, C.C. wrote the first draft of the manuscript, all authors critically revised the draft. All authors revised and approved the final version.

Conflicts of Interest

Carlo Catassi has received consultancy funds from Schär Company (Burgstall, BZ, Italy). Other authors declare no conflict of interest.

References

  1. Gibson, P.; Shepherd, S.J. Personal view: Food for thought—Western lifestyle and susceptibility to Crohn’s disease. The FODMAP hypothesis. Aliment. Pharmacol. Ther. 2005, 21, 1399–1409. [Google Scholar] [CrossRef] [PubMed]
  2. Gibson, P.R.; Shepherd, S.J. Evidence-based dietary management of functional gastrointestinal symptoms: The FODMAP approach. J. Gastroenterol. Hepatol. 2010, 25, 252–258. [Google Scholar] [CrossRef] [PubMed]
  3. Biesiekierski, J.R.; Peters, S.L.; Newnham, E.D.; Rosella, O.; Muir, J.G.; Gibson, P.R. No effects of gluten in patients with self-reported non-celiac gluten sensitivity after dietary reduction of fermentable, poorly absorbed, short-chain carbohydrates. Gastroenterology 2013, 145, 320–328. [Google Scholar] [CrossRef] [PubMed]
  4. Shepherd, S.; Gibson, P. The Complete Low FODMAP Diet: A Revolutionary Plan for Managing IBS and Other Digestive Disorders, 1st ed.; The Experiment, LLC: New York, NY, USA, 2013. [Google Scholar]
  5. McKenzie, Y.A.; Bowyer, R.K.; Leach, H.; Gulia, P.; Horobin, J.; O’Sullivan, N.A.; Pettitt, C.; Reeves, L.B.; Seamark, L.; Williams, M.; et al. British Dietetic Association systematic review and evidence-based practice guidelines for the dietary management of irritable bowel syndrome in adults (2016 update). J. Hum. Nutr. Diet. 2016, 29, 549–575. [Google Scholar] [CrossRef] [PubMed]
  6. Marsh, A.; Eslick, E.M.; Eslick, G.D. Does a diet low in FODMAPs reduce symptoms associated with functional gastrointestinal disorders? A comprehensive systematic review and meta-analysis. Eur. J. Nutr. 2016, 55, 897–906. [Google Scholar] [CrossRef] [PubMed]
  7. Uno, Y.; van Velkinburgh, J.C. Logical hypothesis: Low FODMAP diet to prevent diverticulitis. World. J. Gastrointest. Pharmacol. Ther. 2016, 7, 503–512. [Google Scholar] [CrossRef] [PubMed]
  8. Lis, D.; Ahuja, K.D.; Stellingwerff, T.; Kitic, C.M.; Fell, J. Case Study: Utilizing a Low FODMAP Diet to Combat Exercise-Induced Gastrointestinal Symptoms. Int. J. Sport. Nutr. Exerc. Metab. 2016, 26, 481–487. [Google Scholar] [CrossRef] [PubMed]
  9. Durchschein, F.; Petritsch, W.; Hammer, H.F. Diet therapy for inflammatory bowel diseases: The established and the new. World. J. Gastroenterol. 2016, 22, 2179–2194. [Google Scholar] [PubMed]
  10. Staudacher, H.M.; Irving, P.M.; Lomer, M.C.; Whelan, K. Mechanisms and efficacy of dietary FODMAP restriction in IBS. Nat. Rev. Gastroenterol. Hepatol. 2014, 11, 256–266. [Google Scholar] [CrossRef] [PubMed]
  11. Sabater-Molina, M.; Larqué, E.; Torrella, F.; Zamora, S. Dietary fructooligosaccharides and potential benefits on health. J. Physiol. Biochem. 2009, 65, 315–328. [Google Scholar] [CrossRef] [PubMed]
  12. Andoh, A.; Tsujikawa, T.; Fujiyama, Y. Role of dietary fiber and short-chain fatty acids in the colon. Curr. Pharm. Des. 2003, 9, 347–358. [Google Scholar] [CrossRef] [PubMed]
  13. Blachier, F.; Beaumont, M.; Andriamihaja, M.; Davila, A.M.; Lan, A.; Grauso, M.; Armand, L.; Benamouzig, R.; Tomé, D. Changes in the Luminal Environment of the Colonic Epithelial Cells and Physiopathological Consequences. Am. J. Pathol. 2017, 187, 476–486. [Google Scholar] [CrossRef] [PubMed]
  14. Yao, C.K.; Tan, H.-L.; van Langenberg, D.R.; Barrett, J.S.; Rose, R.; Liels, K.; Gibson, P.-R.; Muir, J.G. Dietary sorbitol and mannitol: Food content and distinct absorption patterns between healthy individuals and patients with irritable bowel syndrome. J. Hum. Nutr. Diet. 2014, 27, S263–S275. [Google Scholar] [CrossRef] [PubMed]
  15. Biesiekierski, J.R.; Rosella, O.; Rose, R.; Liels, K.; Barrett, J.S.; Shepherd, S.J.; Gibson, P.R.; Muir, J.G. Quantification of fructans, galacto-oligosacharides and other short-chain carbohydrates in processed grains and cereals. J. Hum. Nutr. Diet. 2011, 24, 154–176. [Google Scholar] [CrossRef] [PubMed]
  16. Muir, J.G.; Rose, R.; Rosella, O.; Liels, K.; Barrett, J.S.; Shepherd, S.J.; Gibson, P.R. Measurement of Short-Chain Carbohydrates in Common Australian Vegetables and Fruits by High-Performance Liquid Chromatography (HPLC). J. Agric. Food Chem. 2009, 57, 554–565. [Google Scholar] [CrossRef] [PubMed]
  17. Liang, Z.; Sang, M.; Fan, P.; Wu, B.; Wang, L.; Duan, W.; Li, S. Changes of polyphenols, sugars, and organic acid in 5 Vitis genotypes during berry ripening. J. Food Sci. 2011, 76, C1231–C1238. [Google Scholar] [CrossRef] [PubMed]
  18. Shepherd, S.J.; Parker, F.C.; Muir, J.G.; Gibson, P.R. Dietary triggers of abdominal symptoms in patients with irritable bowel syndrome: Randomized placebo-controlled evidence. Clin. Gastroenterol. Hepatol. 2008, 6, 765–771. [Google Scholar] [CrossRef] [PubMed]
  19. Staudacher, H.M.; Whelan, K.; Irving, P.M.; Lomer, M.C. Comparison of symptom response following advice for a diet low in fermentable carbohydrates (FODMAPs) versus standard dietary advice in patients with irritable bowel syndrome. J. Hum. Nutr. Diet. 2011, 24, 487–495. [Google Scholar] [CrossRef] [PubMed]
  20. Staudacher, H.M.; Lomer, M.C.; Anderson, J.L.; Barrett, J.S.; Muir, J.G.; Irving, P.M.; Whelan, K. Fermentable carbohydrate restriction reduces luminal bifidobacteria and gastrointestinal symptoms in patients with irritable bowel syndrome. J. Nutr. 2012, 142, 1510–1518. [Google Scholar] [CrossRef] [PubMed]
  21. De Roest, R.H.; Dobbs, B.R.; Chapman, B.A.; Batman, B.; O’Brien, L.A.; Leeper, J.A.; Hebblethwaite, C.R.; Gearry, R.B. The low FODMAP diet improves gastrointestinal symptoms in patients with irritable bowel syndrome: A prospective study. Int. J. Clin. Pract. 2013, 67, 895–903. [Google Scholar] [CrossRef] [PubMed]
  22. Halmos, E.P.; Christophersen, C.T.; Bird, A.R.; Shepherd, S.J.; Gibson, P.R.; Muir, J.G. Diets that differ in their FODMAP content alter the colonic luminal microenvironment. Gut 2015, 64, 93–100. [Google Scholar] [CrossRef] [PubMed]
  23. Pedersen, N.; Andersen, N.N.; Végh, Z.; Jensen, L.; Ankersen, D.V.; Felding, M.; Simonsen, M.H.; Burisch, J.; Munkholm, P. Ehealth: Low FODMAP diet vs. Lactobacillus rhamnosus GG in irritable bowel syndrome. World. J. Gastroenterol. 2014, 20, 16215–16226. [Google Scholar] [CrossRef] [PubMed]
  24. Chumpitazi, B.P.; Cope, J.L.; Hollister, E.B.; Tsai, C.M.; McMeans, A.R.; Luna, R.A.; Versalovic, J.; Shulman, R.J. Randomised clinical trial: Gut microbiome biomarkers are associated with clinical response to a low FODMAP diet in children with the irritable bowel syndrome. Aliment. Pharmacol. Ther. 2015, 42, 418–427. [Google Scholar] [CrossRef] [PubMed]
  25. Böhn, L.; Störsrud, S.; Liljebo, T.; Collin, L.; Lindfors, P.; Törnblom, H.; Simrén, M. Diet low in FODMAPs reduces symptoms of irritable bowel syndrome as well as traditional dietary advice: A randomized controlled trial. Gastroenterology 2015, 149, 1399–1407. [Google Scholar] [CrossRef] [PubMed]
  26. Whigham, L.; Joyce, T.; Harper, G.; Irving, P.M.; Staudacher, H.M.; Whelan, K.; Lomer, M.C. Clinical effectiveness and economic costs of group versus one-to-one education for short-chain fermentable carbohydrate restriction (low FODMAP diet) in the management of irritable bowel syndrome. J. Hum. Nutr. Diet. 2015, 28, 687–696. [Google Scholar] [CrossRef] [PubMed]
  27. McIntosh, K.; Reed, D.E.; Schneider, T.; Dang, F.; Keshteli, A.H.; de Palma, G.; Madsen, K.; Bercik, P.; Vanner, S. FODMAPs alter symptoms and the metabolome of patients with IBS: A randomised controlled trial. Gut 2016. [Google Scholar] [CrossRef] [PubMed]
  28. Peters, S.L.; Yao, C.K.; Philpott, H.; Yelland, G.W.; Muir, J.G.; Gibson, P.R. Randomised clinical trial: The efficacy of gut-directed hypnotherapy is similar to that of the low FODMAP diet for the treatment of irritable bowel syndrome. Aliment. Pharmacol. Ther. 2016, 44, 447–459. [Google Scholar] [CrossRef] [PubMed]
  29. Laatikainen, R.; Koskenpato, J.; Hongisto, S.M.; Loponen, J.; Poussa, T.; Hillilä, M.; Korpela, R. Randomised clinical trial: Low FODMAP rye bread vs. regular rye bread to relieve the symptoms of irritable bowel syndrome. Aliment. Pharmacol. Ther. 2016, 44, 460–470. [Google Scholar] [CrossRef] [PubMed]
  30. Valeur, J.; Røseth, A.G.; Knudsen, T.; Malmstrøm, G.H.; Fiennes, J.T.; Midtvedt, T.; Berstad, A. Fecal Fermentation in Irritable Bowel Syndrome: Influence of Dietary Restriction of Fermentable Oligosaccharides, Disaccharides, Monosaccharides and Polyols. Digestion 2016, 94, 50–56. [Google Scholar] [CrossRef] [PubMed]
  31. Eswaran, S.L.; Chey, W.D.; Han-Markey, T.; Ball, S.; Jackson, K. A Randomized Controlled Trial Comparing the Low FODMAP Diet vs. Modified NICE Guidelines in US Adults with IBS-D. Am. J. Gastroenterol. 2016, 111, 1824–1832. [Google Scholar] [CrossRef] [PubMed]
  32. Major, G.; Pritchard, S.; Murray, K.; Alappadan, J.P.; Hoad, C.L.; Marciani, L.; Gowland, P.; Spiller, R. Colon Hypersensitivity to Distension, Rather Than Excessive Gas Production, Produces Carbohydrate-Related Symptoms in Individuals With Irritable Bowel Syndrome. Gastroenterology 2017, 152, 124–133. [Google Scholar] [CrossRef] [PubMed]
  33. Hustoft, T.N.; Hausken, T.; Ystad, S.O.; Valeur, J.; Brokstad, K.; Hatlebakk, J.G.; Lied, G.A. Effects of varying dietary content of fermentable short-chain carbohydrates on symptoms, fecal microenvironment, and cytokine profiles in patients with irritable bowel syndrome. Neurogastroenterol. Motil. 2016. [Google Scholar] [CrossRef] [PubMed]
  34. The National Institute for Health and Care Excellence. NICE Clinical Guidelines, No 61. Irritable Bowel Syndrome in Adults: Diagnosis and Management of Irritable Bowel Syndrome in Primary Care; Last Updated: February 2015; National Collaborating Centre for Nursing and Supportive Care: London, UK; Royal College of Nursing: London, UK, February 2008. [Google Scholar]
  35. Maagaard, L.; Ankersen, D.V.; Végh, Z.; Burisch, J.; Jensen, L.; Pedersen, N.; Munkholm, P. Follow-up of patients with functional bowel symptoms treated with a low FODMAP diet. World J. Gastroenterol. 2016, 22, 4009–4019. [Google Scholar] [CrossRef] [PubMed]
  36. Rajilić-Stojanović, M.; Jonkers, D.M.; Salonen, A.; Hanevik, K.; Raes, J.; Jalanka, J.; de Vos, W.M.; Manichanh, C.; Golic, N.; Enck, P.; et al. Intestinal microbiota and diet in IBS: Causes, consequences, or epiphenomena? Am. J. Gastroenterol. 2015, 110, 278–287. [Google Scholar] [CrossRef] [PubMed]
  37. Vici, G.; Belli, L.; Biondi, M.; Polzonetti, V. Gluten free diet and nutrient deficiencies: A review. Clin. Nutr. 2016, 35, 1236–1241. [Google Scholar] [CrossRef] [PubMed]
  38. Infante, D.; Tormo, R. Risk of inadequate bone mineralization in diseases involving long-term suppression of dairy products. J. Pediatr. Gastroenterol. Nutr. 2000, 30, 310–313. [Google Scholar] [CrossRef] [PubMed]
  39. Abrams, S.A.; Griffin, I.J.; Davila, P.M. Calcium and zinc absorption from lactose-containing and lactose-free infant formulas. Am. J. Clin. Nutr. 2002, 76, 442–446. [Google Scholar] [PubMed]
  40. Brewer, M.S. Natural antioxidants: Sources, compounds, mechanisms of action, and potential applications. Compr. Rev. Food Sci. Food Saf. 2011, 10, 221–247. [Google Scholar] [CrossRef]
  41. Gröber, U.; Reichrath, J.; Holick, M.F. Live Longer with Vitamin D? Nutrients 2015, 7, 1871–1880. [Google Scholar] [CrossRef] [PubMed]
Table 1. Clinical trials on the effect of low-FODMAP diet in IBS patients.
Table 1. Clinical trials on the effect of low-FODMAP diet in IBS patients.
First Author, YearPatientsnStudy DesignDiet DurationResultsComment on the Study Design
Shepherd et al. [18]Patients with IBSn = 25Low-FODMAP diet followed by DBPC crossover challenge with fructose and fructane2 weeks70% of patients receiving fructose, 77% receiving fructans, and 79% receiving a mixture reported symptoms were not adequately controlled, compared with 14% receiving glucoseOnly some FODMAPs were tested in this study
Staudacher et al. [19]Consecutive patients with IBSI = 43
C = 39
Low FODMAP vs. standard IBS diet 9 monthsImproved satisfaction and IBS score in I groupLack of randomization
Staudacher et al. [20]Patients with IBSI = 19
C = 22
RCT, Low FODMAPs vs. habitual diet1 weeksMore patients in the intervention group reported adequate control of symptoms (68%) compared with controls (23%)Lack of blinding
Biesiekierski et al. [3]Patients with NCGS and IBSn = 37Low-FODMAP diet followed by DBPC crossover challenge with gluten3 weeksImprovement with low FODMAP diet, no change between gluten and placebo challengeLack of control and no blinding during the low FODMAP diet
De Roest et al. [21]consecutive patients with IBSn = 90Open, low FODMAP diet 16 monthsImprovement of pre-study symptomLack of control group
Halmos et al. [22]Patients with IBS and controlsI = 30
C = 8
Randomized, crossover, low-FODMAP diet vs. typical Australian diet3 weeksLower overall gastrointestinal symptom scores while on a diet low in FODMAPsLack of blinding
Pedersen et al. [23]Patients with IBSI1 = 42
I2 = 41
C = 40
Randomized, controlled trial comparing the low FODMAP diet, treatment with Lactobacillus GG or a control diet6 weeksBoth the low FODMAP diet and treatment with Lactobacillus GG were similarly effectiveLack of blinding
Chumpitazi et al. [24]Children with IBSn = 33Randomized, double-blind, crossover trial, children with Rome III IBS completed a one-week baseline period. They then were randomised to a low FODMAP diet or typical American childhood diet2 daysLess abdominal pain occurred during the low FODMAP diet vs. typical dietComplete blinding unlikely. Short duration of challenge (two days)
Whigham et al. [25]Patients with IBSn = 365Evaluation of low FODMAP diet administered in a dietitian-led group education or traditional one-to-one education6 weeksSignificant decrease in symptom severity from baseline to follow-up for both groups but no difference in symptom response between group and one-to-one educationLack of a control group; no randomization
Böhn et al. [26]Patients with IBSI = 33
C = 34
Multi-center, parallel, single-blind study. Subjects were randomly assigned to for four weeks to a low-FODMAP or standard IBS diet4 weeksThe severity of IBS symptoms was reduced in both groups during the intervention in both groups before vs. at the end of the four-week diet, without a significant difference between the groupsSingle blinding
McIntosh K et al. [27]Patients with IBSI = 19
C = 18
Controlled, single blind study with randomization to a low or high-FODMAP diet for three weeks3 weeksThe IBS severity symptom score (SSS) was reduced in the low-FODMAP diet group but not the high-FODMAP groupSingle blinding
Peters et al. [28]Patients with IBSI1 = 25
I2 = 24
I3 = 25
Consecutive patients were randomised to receive hypnotherapy, low-FODMAP diet or a combination6 weeksImprovements in overall symptoms were observed from baseline to week six for hypnotherapy, diet and combination with no difference across groupsNo control group, no blinding
Laatikainen et al. [29]Patients with IBSn = 87randomised double blind controlled cross-over study. Participants were supplied with both regular rye bread and low-FODMAP rye bread for four weeks4 weeksMany signs of IBS were milder on the low-FODMAP rye bread but no differences were detected in IBS-SSS or quality of lifeWell-designed study; only rye FODMAPs were tested
Valeur et al. [30]Patients with IBSn = 63Consecutive patients participating in a four-week FODMAP-restricted diet4 weeksFollowing the dietary intervention, IBS-SSS scores improved significantlyLack of control group, and lack of blinding
Eswaran et al. [31]Patients with IBS-DI1 = 45
I2 = 39
Single-center, randomized-controlled trial comparing a low-FODMAP with the mNICE diet for four weeks.4 weeks40%–50% of patients reported adequate relief of their IBS-D symptoms with the low-FODMAP diet or a diet based on modified NICE guidelines. The low-FODMAP diet led to significantly greater improvement in individual IBS symptoms, particularly pain and bloatingLack of blinding
Major et al. [32]Patients with IBSn = 58Three-period, cross-over study with a single dose of high- or low-FODMAP drink1 dayMore patients reached the predefined symptom threshold after intake of inulin or fructose than glucose. Controls had lower symptom scores during the period after drink consumption, despite similar MRI parameters and breath hydrogen responsesLack of blinding
Hustoft et al. [33]Patients with IBSn = 20After three weeks of low-FODMAP patients were randomized and double-blindly assigned to receive a supplement of either FOS (FODMAP) or maltodextrin (placebo) for the next 10 days, followed by a three-week washout period before crossover10 daysIrritable bowel syndrome symptoms consistently improved after three weeks of low FOMAP, and significantly more participants reported symptom relief in response to placebo than FOS Only one type of FODMAP was investigated in this study
FODMAP: Fermentable Oligo-, Di- and Mono-saccharides And Polyols; IBS: Irritable bowel syndrome; IBS-D: Irritable bowel syndrome with diarrhea; RCT: randomized controlled trial; NCGS: non celiac gluten sensitivity; DBPC: double-blind placebo-controlled; I: intervention; C: control; SSS: severity symptom score; NICE: National Institute for Health and Care Excellence; FOS: fructo-oligosaccharides; GOS: galacto-oligosaccharides.
Table 2. Common food that need to be excluded from the low-FODMAP diet.
Table 2. Common food that need to be excluded from the low-FODMAP diet.
Food TypeTo be Excluded (High-FODMAP Content)
Cereals and their derivativesWheat, barley, rye
LegumesAll (lentils, beans, chickpeas, soy, peas)
VegetablesArtichokes, asparagus, cauliflower, garlic, leeks, mushrooms, onions, scallions, shallots, snow peas
FruitApples, apricots, Asian pears, blackberries, cherries, figs, jackfruit, mangoes, nectarines, peaches, pears, persimmon, plums, prunes, tamarillo, watermelon, white peaches, grape
Dairy productsRegular milk, ice cream, soft cheeses, yogurt

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Catassi, G.; Lionetti, E.; Gatti, S.; Catassi, C. The Low FODMAP Diet: Many Question Marks for a Catchy Acronym. Nutrients 2017, 9, 292. https://doi.org/10.3390/nu9030292

AMA Style

Catassi G, Lionetti E, Gatti S, Catassi C. The Low FODMAP Diet: Many Question Marks for a Catchy Acronym. Nutrients. 2017; 9(3):292. https://doi.org/10.3390/nu9030292

Chicago/Turabian Style

Catassi, Giulia, Elena Lionetti, Simona Gatti, and Carlo Catassi. 2017. "The Low FODMAP Diet: Many Question Marks for a Catchy Acronym" Nutrients 9, no. 3: 292. https://doi.org/10.3390/nu9030292

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