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腹泻型肠易激综合征患者粪便初级胆汁酸增加和肠道菌群失调。

Increase in fecal primary bile acids and dysbiosis in patients with diarrhea-predominant irritable bowel syndrome.

机构信息

Hepato Gastro Enterology Department, Louis Mourier Hospital, University Paris VII, AP-HP, Colombes, France.

出版信息

Neurogastroenterol Motil. 2012 Jun;24(6):513-20, e246-7. doi: 10.1111/j.1365-2982.2012.01893.x. Epub 2012 Feb 22.

Abstract

BACKGROUND

Irritable bowel syndrome (IBS) is a multifactorial disease for which a dysbiosis of the gut microbiota has been described. Bile acids (BA) could play a role as they are endogenous laxatives and are metabolized by gut microbiota. We compared fecal BA profiles and microbiota in healthy subjects (HS) and patients with diarrhea-predominant IBS (IBS-D), and we searched for an association with symptoms.

METHODS

Clinical features and stool samples were collected in IBS-D patients and HS. Fecal BA profiles were generated using HPLC coupled to tandem mass spectrometry. The fecal microbiota composition was assessed by q-PCR targeting dominant bacterial groups and species implicated in BA transformation.

KEY RESULTS

Fourteen IBS-D patients and 18 HS were included. The two groups were comparable in terms of age and sex. The percentage of fecal primary BA was significantly higher in IBS-D patients than in HS, and it was significantly correlated with stool consistency and frequency. Fecal counts of all bacteria, lactobacillus, coccoides, leptum and Faecalibacterium prausnitzii were similar. There was a significant increase of Escherichia coli and a significant decrease of leptum and bifidobacterium in IBS-D patients.

CONCLUSIONS & INFERENCES: We report an increase of primary BA in the feces of IBS-D patients compared to HS, correlated with stool consistency and frequency. A dysbiosis of different bacterial groups was detected, some of them involved in BA transformation. As the gut microbiota is the exclusive pathway to transform primary into secondary BA, this suggests a functional consequence of dysbiosis, leading to lower BA transformation.

摘要

背景

肠易激综合征(IBS)是一种多因素疾病,其肠道微生物群失调已被描述。胆汁酸(BA)可能起作用,因为它们是内源性泻药,并被肠道微生物群代谢。我们比较了健康受试者(HS)和腹泻为主的肠易激综合征(IBS-D)患者的粪便 BA 谱和微生物群,并寻找与症状的关联。

方法

在 IBS-D 患者和 HS 中收集临床特征和粪便样本。使用 HPLC 与串联质谱联用生成粪便 BA 谱。通过靶向参与 BA 转化的主要细菌群和物种的 q-PCR 评估粪便微生物群组成。

主要结果

纳入了 14 名 IBS-D 患者和 18 名 HS。两组在年龄和性别方面具有可比性。IBS-D 患者粪便初级 BA 的百分比明显高于 HS,与粪便稠度和频率显著相关。所有细菌、乳杆菌、球菌、雷普氏菌和普拉梭菌的粪便计数相似。IBS-D 患者的大肠杆菌数量显著增加,雷普氏菌和双歧杆菌数量显著减少。

结论和推论

我们报告了 IBS-D 患者粪便中初级 BA 的增加与粪便稠度和频率相关。检测到不同细菌群的失调,其中一些涉及 BA 转化。由于肠道微生物群是将初级 BA 转化为次级 BA 的唯一途径,这表明失调的功能后果,导致 BA 转化降低。

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