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肠道微生物群会影响心房节律吗?因果关系和推测。

Does gut microbiota affect atrial rhythm? Causalities and speculations.

机构信息

Department of Cardiology, Maastricht University Medical Centre and Cardiovascular Research Institute Maastricht, Universiteitssingel 50, 6229 ER Maastricht, the Netherlands.

Department of Biomedical Sciences, Faculty of Health and Medical Sciences, University of Copenhagen, Blegdamsvej 3B, 2200 Copenhagen, Denmark.

出版信息

Eur Heart J. 2021 Sep 14;42(35):3521-3525. doi: 10.1093/eurheartj/ehab467.

DOI:10.1093/eurheartj/ehab467
PMID:34338744
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8442110/
Abstract

Dietary intake has been shown to change the composition of gut microbiota and some changes in microbiota (dysbiosis) have been linked to diabetes, hypertension, and obesity, which are established risk factors for atrial fibrillation (AF). In addition, intestinal dysbiosis generates microbiota-derived bioactive metabolites that might exert proarrhythmic actions. Although emerging preclinical investigations and clinical observational cohort studies suggest a possible role of gut dysbiosis in AF promotion, the exact mechanisms through which dysbiosis contributes to AF remain unclear. This Viewpoint article briefly reviews evidence suggesting that abnormalities in the intestinal microbiota play an important and little-recognized role in the pathophysiology of AF and that an improved understanding of this role may open up new possibilities in the management of AF.

摘要

饮食摄入已被证明会改变肠道微生物群的组成,而微生物群的一些变化(失调)与糖尿病、高血压和肥胖有关,这些都是心房颤动(AF)的既定风险因素。此外,肠道失调会产生可能产生致心律失常作用的微生物衍生生物活性代谢物。尽管新兴的临床前研究和临床观察队列研究表明肠道失调在促进 AF 方面可能起作用,但失调如何导致 AF 的确切机制尚不清楚。本文观点简要回顾了一些证据,表明肠道微生物组的异常在 AF 的病理生理学中起着重要而尚未被认识的作用,对这一作用的深入了解可能为 AF 的治疗开辟新的可能性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e357/8442110/f1535bcfe526/ehab467f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e357/8442110/f1535bcfe526/ehab467f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e357/8442110/f1535bcfe526/ehab467f1.jpg

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2
NLRP3 inflammasome is a key driver of obesity-induced atrial arrhythmias.NLRP3 炎性小体是肥胖诱导的心房心律失常的关键驱动因素。
Cardiovasc Res. 2021 Jun 16;117(7):1746-1759. doi: 10.1093/cvr/cvab024.
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Trimethylamine N-oxide in atrial fibrillation progression.
心房颤动中的代谢组学:揭示用于诊断、预后和个性化治疗的新型生物标志物和途径。
J Clin Med. 2024 Dec 25;14(1):34. doi: 10.3390/jcm14010034.
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Intestinal Microbiota and Derived Metabolites in Myocardial Fibrosis and Postoperative Atrial Fibrillation.肠道微生物群及其衍生代谢物与心肌纤维化和术后心房颤动。
Int J Mol Sci. 2024 May 30;25(11):6037. doi: 10.3390/ijms25116037.
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