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肠易激综合征中的肠道微生物群特征与调节

Gut microbiota signatures and modulation in irritable bowel syndrome.

作者信息

Marasco Giovanni, Cremon Cesare, Barbaro Maria Raffaella, Stanghellini Vincenzo, Barbara Giovanni

机构信息

Division of Internal Medicine, IRCCS Azienda Ospedaliero-Universitaria di Bologna, Bologna 40138, Italy.

Department of Medical and Surgical Sciences, Alma Mater Studiorum Università di Bologna, Bologna 40138, Italy.

出版信息

Microbiome Res Rep. 2022 Mar 5;1(2):11. doi: 10.20517/mrr.2021.12. eCollection 2022.

Abstract

Irritable bowel syndrome (IBS) affects approximately one tenth of the general population and is characterized by abdominal pain associated with abnormalities in bowel habits. Visceral hypersensitivity, abnormal intestinal motor function, mucosal immune activation, and increased intestinal permeability concur to its pathophysiology. Psychological factors can influence symptom perception at the central nervous system level. In addition, recent evidence suggests that dysbiosis may be a key pathophysiological factor in patients with IBS. Increasing understanding of the pathophysiological mechanisms translates into new and more effective therapeutic approaches. Indeed, in line with this evidence, IBS therapies nowadays include agents able to modulate gut microbiota function and composition, such as diet, prebiotics, probiotics, and antibiotics. In addition, in the last decade, an increasing interest in fecal microbiota transplantation has been paid. An in-depth understanding of the intestinal microenvironment through accurate faucal microbiota and metabolite analysis may provide valuable insights into the pathophysiology of IBS, finally shaping new tailored IBS therapies.

摘要

肠易激综合征(IBS)影响着约十分之一的普通人群,其特征为腹痛伴排便习惯异常。内脏高敏感性、肠道运动功能异常、黏膜免疫激活以及肠道通透性增加共同参与其病理生理过程。心理因素可在中枢神经系统层面影响症状感知。此外,最近有证据表明,肠道菌群失调可能是肠易激综合征患者的关键病理生理因素。对病理生理机制的深入理解带来了新的、更有效的治疗方法。事实上,基于这一证据,如今肠易激综合征的治疗方法包括能够调节肠道微生物群功能和组成的药物,如饮食、益生元、益生菌和抗生素。此外,在过去十年中,人们对粪便微生物群移植的兴趣与日俱增。通过精确的粪便微生物群和代谢物分析深入了解肠道微环境,可能为肠易激综合征的病理生理学提供有价值的见解,最终形成新的个性化肠易激综合征治疗方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/78d2/10688783/7f38b57c8552/mrr-1-2-11.fig.1.jpg

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