Irritable bowel syndrome (IBS) is one of the most common functional gastrointestinal disorders. About 5–11% of the population in most countries is assumed to have IBS.1 The symptoms of this disorder include recurrent abdominal pain or discomfort related to bowel habit changes that continue for > 6 months, causing heavy burden on the quality of life of some affected persons.1,2 The mechanism behind IBS is considered to be multifactorial, including altered motility, visceral hypersensitivity, altered gut microbiota, and dysfunction of the brain-gut axis and the immune system.1,2 Likewise, there are multiple treatment options for this disorder, and selecting the appropriate treatment may be challenging for patients and clinicians in the presence of limited evidence.1
Recent studies have shed new insights about the role of food on the etiologies of IBS. There are many evidences indicating that certain foods cause IBS symptoms. The elimination diets, such as low fermentable, oligosaccharides, disaccharides, monosaccharides, and polyols (FODMAPs), have been shown to alleviate symptoms.3,4 Fructose is a monosaccharide that is increasingly consumed as dietary habits become Westernized worldwide. The more extensive use of fructose-containing artificial sweeteners and high-fructose corn syrup are definitely contributing to this increased intake.5,6 A French cohort study showed that this Westernized dietary pattern moderately increased the risk of IBS,7 and one of the reported food-related etiologies of IBS is fructose malabsorption (FM).8,9
The ability of the human intestines to absorb fructose is limited. Specific intestinal fructose transporters (glucose transporter-5) in the intestines of humans may be easily overwhelmed by fructose > 50 g.10 FM leads to a variety of gastrointestinal intolerance symptoms that resemble the symptoms presented by patients with IBS. When patients with unexplained symptoms were administered 50 g fructose and underwent breath tests, 73% tested positive for elevated hydrogen or methane, providing evidence of FM. Moreover, approximately 80% of these positive-tested patients experienced symptoms such as flatus, pain, bloating, belching, and altered bowel habit.11 The osmotic load that the unabsorbed fructose creates passes into the colon, which houses a variety of fermenting microbiomes that produce these unpleasant symptoms.8
The physiological connection between FM and IBS is becoming more concrete. Patients with IBS without small intestine bacterial overgrowth (SIBO), confirmed with the glucose hydrogen breath test (HBT), who were loaded with 25 g fructose showed symptomatic FM and fructose intolerance without malabsorption in 22% and 28%, respectively.12 Forty-four percent of patients experiencing functional bowel disorders showed FM after being administered 25 g fructose, whereas 60% showed improvement after lowering the fructose level in their diet.13 Another study observed that 52% of patients with IBS had FM, in contrast to 16% of the control group and the IBS patients with FM tended to be IBS-D (IBS with predominant diarrhea) type.14
Many evidences about the relationship between FM and IBS highlight the importance of HBT that is a safe, inexpensive, and noninvasive modality for diagnosing carbohydrate malabsorption. The HBT is clinically applied to assess carbohydrate malabsorption in patients with dietary restrictions, such as those under a low fermentable carbohydrate diet (eg, FODMAP).15,16 Other clinical uses of this test include diagnosing SIBO and measuring the orocecal transit time.17,18 However, there are several problems. The HBT is not yet a standardized test, and SIBO may increase the positive rates of FM when measured using the glucose HBT, because this test cannot measure fermented gas produced by bacteria in distal small intestine.18
In the current issue of the Journal of Neurogastroenterology and Motility, Jung et al19 published a prospective, controlled study that investigated the prevalence of FM in patients with IBS and in asymptomatic controls after excluding SIBO with the glucose HBT. By excluding patients with a diagnosis of SIBO, attempts were made to better objectively assess the possible relationship between FM and IBS. The 25-g fructose HBT identified FM at a significantly higher percentage in SIBO-negative patients with IBS than in asymptomatic controls, suggesting that FM may be associated with IBS.
The study by Jung et al19 shows the link between IBS and FM; however, it has a few limitations. First, this study included 10 (29%) patients with IBS-C (IBS with predominant constipation). As FM usually presents symptoms related to IBS-D or IBS-M (IBS with mixed bowel habit), the results might have been somewhat altered by including patients with IBS-C. It might have led to better results if only patients with IBS-D and IBS-M were included. Second, as aforementioned, the glucose HBT can not detect bacterial overgrowth in the distal small bowel; thus, some patients classified as having FM might have included those with SIBO.
The prevalence of SIBO is generally higher in patients with IBS than in healthy persons.17,20,21 If SIBO is present, the symptoms associated with FM may become worse owing to bacterial fermentation in the small intestine and in the colon. Therefore, investigating how FM and SIBO interact with each other and lead to the development of IBS symptoms could be an interesting study. In such a study, the symptoms after taking fructose can be compared between patients with IBS with SIBO and patients with IBS without SIBO. In addition, as bloating and flatulence are likely to be caused by increased bacterial fermentation in the bowel, it may be meaningful to explore the association between intestinal bacterial composition and symptom generation, as well as the effect of antibiotics such as rifaximin in patients with FM.
The treatments for patients with IBS are still targeted toward symptoms rather than the pathophysiology behind them. The close association between FM and IBS may suggest more specific and detailed diet plans and treatment considerations for patients with IBS. However, IBS is a disease entity that results from numerous and variable mechanisms, and many confounding factors can make the relationship between FM and IBS less clear. Thus, further well-designed studies are needed to investigate the association between FM and IBS, the underlying mechanisms, and the effectiveness of fructose-eliminating diets.
Footnotes
Financial support: This work was supported by the National Research Foundation of Korea (NRF) grant funded by the Korea government (MEST) (No. 2017R1D1A1B03031924).
Conflicts of interest: None.
References
- 1.Spiller R, Aziz Q, Creed F, et al. Guidelines on the irritable bowel syndrome: mechanisms and practical management. Gut. 2007;56:1770–1798. doi: 10.1136/gut.2007.119446. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 2.Mearin F, Lacy BE, Chang L, et al. Bowel disorders. Gastroenterology. 2016;150:1393–1407. doi: 10.1053/j.gastro.2016.02.031. [DOI] [PubMed] [Google Scholar]
- 3.Schumann D, Klose P, Lauche R, Dobos G, Langhorst J, Cramer H. Low fermentable, oligo-, di-, mono-saccharides and polyol diet in the treatment of irritable bowel syndrome: a systematic review and meta-analysis. Nutrition. 2018;45:24–31. doi: 10.1016/j.nut.2017.07.004. [DOI] [PubMed] [Google Scholar]
- 4.Singh R, Salem A, Nanavati J, Mullin GE. The role of diet in the treatment of irritable bowel syndrome: a systematic review. Gastroenterol Clin North Am. 2018;47:107–137. doi: 10.1016/j.gtc.2017.10.003. [DOI] [PubMed] [Google Scholar]
- 5.Park YK, Yetley EA. Intakes and food sources of fructose in the United States. Am J Clin Nutr. 1993;58:737S–747S. doi: 10.1093/ajcn/58.5.737S. [DOI] [PubMed] [Google Scholar]
- 6.Tappy L. Fructose-containing caloric sweeteners as a cause of obesity and metabolic disorders. J Exp Biol. 2018;221:jeb 164202. doi: 10.1242/jeb.164202. [DOI] [PubMed] [Google Scholar]
- 7.Buscail C, Sabate JM, Bouchoucha M, et al. Western dietary pattern is associated with irritable bowel syndrome in the French NutriNet cohort. Nutrients. doi: 10.3390/nu9090986. Published Online First: 7 Sep 2017. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 8.DiNicolantonio JJ, Lucan SC. Is fructose malabsorption a cause of irritable bowel syndrome? Med Hypotheses. 2015;85:295–297. doi: 10.1016/j.mehy.2015.05.019. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 9.Goebel-Stengel M, Stengel A, Schmidtmann M, Voort I, Kobelt P, Mönnikes H. Unclear abdominal discomfort: pivotal role of carbohydrate malabsorption. J Neurogastroenterol Motil. 2014;20:228–235. doi: 10.5056/jnm.2014.20.2.228. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 10.Rao SS, Attaluri A, Anderson L, Stumbo P. Ability of the normal human small intestine to absorb fructose: evaluation by breath testing. Clin Gastroenterol Hepatol. 2007;5:959–963. doi: 10.1016/j.cgh.2007.04.008. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 11.Choi YK, Johlin FC, Jr, Summers RW, Jackson M, Rao SS. Fructose intolerance: an under-recognized problem. Am J Gastroenterol. 2003;98:1348–1353. doi: 10.1111/j.1572-0241.2003.07476.x. [DOI] [PubMed] [Google Scholar]
- 12.Melchior C, Gourcerol G, Déchelotte P, Leroi AM, Ducrotté P. Symptomatic fructose malabsorption in irritable bowel syndrome: a prospective study. United European Gastroenterol J. 2014;2:131–137. doi: 10.1177/2050640614521124. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 13.Goldstein R, Braverman D, Stankiewicz H. Carbohydrate malabsorption and the effect of dietary restriction on symptoms of irritable bowel syndrome and functional bowel complaints. Isr Med Assoc J. 2000;2:583–587. [PubMed] [Google Scholar]
- 14.Reyes-Huerta JU, de la Cruz-Patiño E, Ramírez-Gutiérrez de Velasco A, Zamudio C, Remes-Troche JM. [Fructose intolerance in patients with irritable bowel syndrome: a case-control study]. Rev Gastroenterol Mex. 2010;75:405–411. [Spanish] [PubMed] [Google Scholar]
- 15.Rana SV, Malik A. Breath tests and irritable bowel syndrome. World J Gastroenterol. 2014;20:7587–7601. doi: 10.3748/wjg.v20.i24.7587. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 16.Yao CK, Tuck CJ. The clinical value of breath hydrogen testing. J Gastroenterol Hepatol. 2017;32(suppl 1):20–22. doi: 10.1111/jgh.13689. [DOI] [PubMed] [Google Scholar]
- 17.Ford AC, Spiegel BM, Talley NJ, Moayyedi P. Small intestinal bacterial overgrowth in irritable bowel syndrome: systematic review and meta-analysis. Clin Gastroenterol Hepatol. 2009;7:1279–1286. doi: 10.1016/j.cgh.2009.06.031. [DOI] [PubMed] [Google Scholar]
- 18.Yu D, Cheeseman F, Vanner S. Combined oro-caecal scintigraphy and lactulose hydrogen breath testing demonstrate that breath testing detects oro-caecal transit, not small intestinal bacterial overgrowth in patients with IBS. Gut. 2011;60:334–340. doi: 10.1136/gut.2009.205476. [DOI] [PubMed] [Google Scholar]
- 19.Jung KW, Seo M, Cho YH, et al. Prevalence of fructose malabsorption in patients with irritable bowel syndrome after excluding small intestinal bacterial overgrowth. J Neurogastroenterol Motil. 2018;24:307–316. doi: 10.5056/jnm17044. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 20.Ghoshal UC, Kumar S, Mehrotra M, Lakshmi C, Misra A. Frequency of small intestinal bacterial overgrowth in patients with irritable bowel syndrome and chronic non-specific diarrhea. J Neurogastroenterol Motil. 2010;16:40–46. doi: 10.5056/jnm.2010.16.1.40. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 21.Shimura S, Ishimura N, Mikami H, et al. Small intestinal bacterial overgrowth in patients with refractory functional gastrointestinal disorders. J Neurogastroenterol Motil. 2016;22:60–68. doi: 10.5056/jnm15116. [DOI] [PMC free article] [PubMed] [Google Scholar]