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Alterations in fecal short-chain fatty acids in patients with irritable bowel syndrome: A systematic review and meta-analysis.

作者信息

Sun Qinghua, Jia Qiong, Song Lijin, Duan Liping

机构信息

Department of Gastroenterology, Peking University Third Hospital, No. 49 North Garden Rd., Haidian District, Beijing, 100191, China.

出版信息

Medicine (Baltimore). 2019 Feb;98(7):e14513. doi: 10.1097/MD.0000000000014513.


DOI:10.1097/MD.0000000000014513
PMID:30762787
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6408019/
Abstract

BACKGROUND: Recent studies indicate that gut microbiota disorders potentially contribute to the pathogenesis of irritable bowel syndrome (IBS), which can be partly reflected by fecal short-chain fatty acids (SCFAs) generated from gut microbiota. Previous studies on SCFA alterations in patients with IBS have yielded conflicting results. No prior systematic review has been conducted on the alterations in fecal SCFAs in IBS patients. AIMS: We performed a meta-analysis to explore and clarify alterations in fecal SCFAs in IBS patients. METHODS: Case-control studies, randomized controlled trials (RCTs), and self-controlled studies were identified through electronic database searches. The standardized mean difference (SMD) with 95% confidence interval (CI) in fecal SCFA levels between different groups was calculated. RESULTS: The proportion of fecal propionate in patients with IBS was significantly higher than in healthy controls (HCs) (SMD = 0.44, 95% CI = 0.12, 0.76). A subgroup analysis showed that the concentration of fecal propionate (SMD = -0.91, 95% CI = -1.41, -0.41) and butyrate (SMD = -0.53, 95% CI = -1.01, -0.04) in patients with constipation-predominant IBS (IBS-C) was significantly lower than that in HCs, and the concentration of fecal butyrate in patients with diarrhea-predominant IBS (IBS-D) was higher than that in HCs (SMD = 0.34, 95% CI = 0.00, 0.67). Finally, we found that restricted diets correlated with fecal butyrate reduction in IBS (SMD = -0.26, 95% CI = -0.51, -0.01). CONCLUSIONS: In terms of fecal SCFAs, there were differences between patients with IBS and HCs. In IBS-C patients, propionate and butyrate were reduced, whereas butyrate was increased in IBS-D patients in comparison to HCs. Propionate and butyrate could be used as biomarkers for IBS diagnosis.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/866d/6408019/475fad2fbe69/medi-98-e14513-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/866d/6408019/4c581d3367ed/medi-98-e14513-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/866d/6408019/3b8f58aa6ade/medi-98-e14513-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/866d/6408019/fd7c050e616c/medi-98-e14513-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/866d/6408019/54cbd66cfe99/medi-98-e14513-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/866d/6408019/475fad2fbe69/medi-98-e14513-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/866d/6408019/4c581d3367ed/medi-98-e14513-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/866d/6408019/3b8f58aa6ade/medi-98-e14513-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/866d/6408019/fd7c050e616c/medi-98-e14513-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/866d/6408019/54cbd66cfe99/medi-98-e14513-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/866d/6408019/475fad2fbe69/medi-98-e14513-g007.jpg

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Alterations in fecal short-chain fatty acids in patients with irritable bowel syndrome: A systematic review and meta-analysis.

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引用本文的文献

[1]
Gut microbiota-derived short-chain fatty acids and their role in human health and disease.

Nat Rev Microbiol. 2025-5-13

[2]
The role of the esophageal and intestinal microbiome in gastroesophageal reflux disease: past, present, and future.

Front Immunol. 2025-2-21

[3]
Exploring Gut Microbiota Imbalance in Irritable Bowel Syndrome: Potential Therapeutic Effects of Probiotics and Their Metabolites.

Nutrients. 2024-12-31

[4]
The Role of Gut Microbiome in Irritable Bowel Syndrome: Implications for Clinical Therapeutics.

Biomolecules. 2024-12-21

[5]
Effects of a Protease Inhibitor Camostat Mesilate on Gut Microbial Function in Patients with Irritable Bowel Syndrome: A Pilot Randomized Placebo-Controlled Study.

Digestion. 2024-11-25

[6]
Novel hypothesis and therapeutic interventions for irritable bowel syndrome: interplay between metal dyshomeostasis, gastrointestinal dysfunction, and neuropsychiatric symptoms.

Mol Cell Biochem. 2025-5

[7]
Modulating the gut microenvironment as a treatment strategy for irritable bowel syndrome: a narrative review.

Gut Microbiome (Camb). 2022-8-25

[8]
Gas Chromatography-Mass Spectrometry-Based Analyses of Fecal Short-Chain Fatty Acids (SCFAs): A Summary Review and Own Experience.

Biomedicines. 2024-8-20

[9]
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[10]
The role and therapeutic effectiveness of seed husk (psyllium husk) in the prevention and non-pharmacological treatment of gastrointestinal diseases. Part 1. Clinical use of psyllium husk in the treatment of irritable bowel syndrome, ulcerative colitis, and colorectal cancer.

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本文引用的文献

[1]
Impact of dietary fiber supplementation on modulating microbiota-host-metabolic axes in obesity.

J Nutr Biochem. 2018-11-26

[2]
Fecal Short Chain Fatty Acids and Dietary Intake in Italian Women With Restrictive Anorexia Nervosa: A Pilot Study.

Front Nutr. 2018-11-29

[3]
Butyrate Producers as Potential Next-Generation Probiotics: Safety Assessment of the Administration of to Healthy Volunteers.

mSystems. 2018-11-6

[4]
Effect of CNCM I-1572 on symptoms, gut microbiota, short chain fatty acids, and immune activation in patients with irritable bowel syndrome: A pilot randomized clinical trial.

United European Gastroenterol J. 2018-5

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Fecal Clostridiales distribution and short-chain fatty acids reflect bowel habits in irritable bowel syndrome.

Environ Microbiol. 2018-9-24

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Irritable Bowel Syndrome.

N Engl J Med. 2017-6-29

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Am J Nurs. 2017-6

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The human intestinal microbiota of constipated-predominant irritable bowel syndrome patients exhibits anti-inflammatory properties.

Sci Rep. 2016-12-16

[9]
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. 2017-4

[10]
Identification of an Intestinal Microbiota Signature Associated With Severity of Irritable Bowel Syndrome.

Gastroenterology. 2016-10-7

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