Gut‐brain axis dysfunction underlies FODMAP‐induced symptom generation in irritable bowel syndrome

Summary Background FODMAPs produce similar small bowel water and colonic gas in patients with irritable bowel syndrome (IBS) and healthy controls (HCs), despite IBS patients reporting increased gastrointestinal (GI) symptoms. Aim To unravel the mechanisms underlying FODMAP‐induced symptom reporting,...

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Veröffentlicht in:Alimentary pharmacology & therapeutics 2022-03, Vol.55 (6), p.670-682
Hauptverfasser: Wu, Jie, Masuy, Imke, Biesiekierski, Jessica R, Fitzke, Heather E, Parikh, Chinar, Schofield, Laurel, Shaikh, Hafsa, Bhagwanani, Anisha, Aziz, Qasim, Taylor, Stuart A, Tack, Jan, Van Oudenhove, Lukas
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Sprache:eng
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Zusammenfassung:Summary Background FODMAPs produce similar small bowel water and colonic gas in patients with irritable bowel syndrome (IBS) and healthy controls (HCs), despite IBS patients reporting increased gastrointestinal (GI) symptoms. Aim To unravel the mechanisms underlying FODMAP‐induced symptom reporting, we investigated gut and brain responses to fructan administration in IBS patients and HC. Methods This randomised, double‐blind, cross‐over study consisted of three visits where fructans (40 g/500 mL saline), glucose (40 g/500 mL saline) or saline (500 mL) were infused intragastrically during 1 h MR brain scanning; abdominal MRI was performed before, 1 h, and 2 h post‐infusion. Symptoms were rated using validated scales. Results In IBS (n = 13), fructans induced more cramps, pain, flatulence and nausea compared to glucose (P = 0.03, 0.001, 0.009 and  0.14), with between‐group differences for cramps and nausea (P = 0.004 and 0.023). Fructans increased small bowel motility and ascending colonic gas and volume equally in IBS and HC (between‐group P > 0.25). The difference in colonic gas between fructans and saline covaried with differences in bloating and cramps in IBS (P = 0.008 and 0.035 respectively). Pain‐related brain regions responded differentially to fructans in IBS compared to HC, including the cerebellum, supramarginal gyrus, anterior and midcingulate cortex, insula and thalamus (pFWE‐corrected 
ISSN:0269-2813
1365-2036
DOI:10.1111/apt.16812