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肠道微生物群在慢性低度炎症中作为动脉粥样硬化性心血管疾病潜在驱动因素的作用:系统评价人类研究。

Role of gut microbiota in chronic low-grade inflammation as potential driver for atherosclerotic cardiovascular disease: a systematic review of human studies.

机构信息

Department of Internal Medicine, Radboud University Medical Center, Nijmegen, The Netherlands.

Department of Genetics, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands.

出版信息

Obes Rev. 2018 Dec;19(12):1719-1734. doi: 10.1111/obr.12750. Epub 2018 Aug 24.

DOI:10.1111/obr.12750
PMID:30144260
Abstract

A hallmark of obesity is chronic low-grade inflammation, which plays a major role in the process of atherosclerotic cardiovascular disease (ACVD). Gut microbiota is one of the factors influencing systemic immune responses, and profound changes have been found in its composition and metabolic function in individuals with obesity. This systematic review assesses the association between the gut microbiota and markers of low-grade inflammation in humans. We identified 14 studies which were mostly observational and relatively small (n = 10 to 471). The way in which the microbiome is analysed differed extensively between these studies. Lower gut microbial diversity was associated with higher white blood cell counts and high sensitivity C-reactive protein (hsCRP) levels. The abundance of Bifidobacterium, Faecalibacterium, Ruminococcus and Prevotella were inversely related to different markers of low-grade inflammation such as hsCRP and interleukin (IL)-6. In addition, this review speculates on possible mechanisms through which the gut microbiota can affect low-grade inflammation and thereby ACVD. We discuss the associations between the microbiome and the inflammasome, the innate immune system, bile acids, gut permeability, the endocannabinoid system and TMAO. These data reinforce the importance of human research into the gut microbiota as potential diagnostic and therapeutic strategy to prevent ACVD.

摘要

肥胖的一个标志是慢性低度炎症,它在动脉粥样硬化性心血管疾病(ACVD)的发生过程中起着重要作用。肠道微生物群是影响全身免疫反应的因素之一,在肥胖个体中,其组成和代谢功能发生了深刻的变化。本系统评价评估了肠道微生物群与人类低度炎症标志物之间的关系。我们确定了 14 项研究,这些研究大多是观察性的,且规模相对较小(n=10 至 471)。这些研究之间的微生物组分析方法差异很大。肠道微生物多样性较低与白细胞计数和高敏 C 反应蛋白(hsCRP)水平升高有关。双歧杆菌、粪杆菌、真杆菌和普雷沃氏菌的丰度与 hsCRP 和白细胞介素(IL)-6 等不同的低度炎症标志物呈负相关。此外,本综述推测了肠道微生物群可能通过何种机制影响低度炎症,从而影响 ACVD。我们讨论了微生物组与炎症小体、先天免疫系统、胆汁酸、肠道通透性、内源性大麻素系统和 TMAO 之间的关联。这些数据强调了人类对肠道微生物群作为预防 ACVD 的潜在诊断和治疗策略的重要性。

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