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心房颤动、血栓栓塞风险与利钠肽的潜在作用,聚焦于脑钠肽和N末端脑钠肽原——一篇叙述性综述

Atrial Fibrillation, thromboembolic risk, and the potential role of the natriuretic peptides, a focus on BNP and NT-proBNP - A narrative review.

作者信息

Kerr Brian, Brandon Lisa

机构信息

Department of Cardiology, St James Hospital, James Street, Dublin 8, Ireland.

出版信息

Int J Cardiol Heart Vasc. 2022 Oct 10;43:101132. doi: 10.1016/j.ijcha.2022.101132. eCollection 2022 Dec.

DOI:10.1016/j.ijcha.2022.101132
PMID:36246770
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9562601/
Abstract

Atrial fibrillation (AF) is one of the most commonly encountered arrythmia in clinical practice. AF itself can be driven by genetic predisposition, ectopic electrical activity, and abnormal atrial tissue substrates. Often there is no single etiological mechanism, but rather a combination of factors that feed back to remodel and worsen tissue substrate, "AF begets AF". The clinical consequences of AF can often include emboli, heart failure, and early mortality. The classical AF cardioembolic (CE) concept requires thrombus formation in the left atrial appendage, with subsequent embolization. The temporal dissociation between AF occurrence and CE events has thrown doubt on AF as the driver of this mechanism. Instead, there has been a resurgence of the "atrial cardiomyopathy" (ACM) concept. An ACM is proposed as a potential mechanism of embolic disease through promotion of prothrombotic mechanisms, with AF instead reflecting atrial disease severity. Regardless, AF has been implicated in 25% to 30% of cryptogenic strokes. Natriuretic peptide(NP)s have been shown to be elevated in AF, with higher levels of both NT-proBNP and BNP being predictive of incidental AF. NPs potentially reflect the atrial environment and could be used to identify an underlying ACM. Therefore, this narrative review examines this evidence and mechanisms that may underpin the role of NPs in identifying atrial dysfunction, with focus on both, BNP and NTproBNP. We explore their potential role in the prediction and screening for both, ACM and AF. Moreover, we compare both NPs directly to ascertain a superior biomarker.

摘要

心房颤动(AF)是临床实践中最常遇到的心律失常之一。AF本身可由遗传易感性、异位电活动和异常的心房组织基质驱动。通常不存在单一的病因机制,而是多种因素相互作用,导致组织基质重塑并恶化,即“AF引发AF”。AF的临床后果通常包括栓塞、心力衰竭和早期死亡。经典的AF心脏栓塞(CE)概念要求在左心耳形成血栓,随后发生栓塞。AF发作与CE事件之间的时间分离使人们对AF作为这种机制的驱动因素产生了怀疑。相反,“心房心肌病”(ACM)概念重新兴起。有人提出ACM是通过促进血栓形成机制导致栓塞性疾病的潜在机制,而AF则反映心房疾病的严重程度。无论如何,AF与25%至30%的隐源性卒中有关。利钠肽(NP)在AF中已被证明升高,NT-proBNP和BNP水平升高均提示偶发性AF。NP可能反映心房环境,可用于识别潜在的ACM。因此,本叙述性综述探讨了可能支持NP在识别心房功能障碍中作用的证据和机制,重点关注BNP和NTproBNP。我们探讨了它们在ACM和AF的预测和筛查中的潜在作用。此外,我们直接比较这两种NP,以确定更优的生物标志物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/367a/9562601/6791acf6c5e7/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/367a/9562601/6791acf6c5e7/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/367a/9562601/6791acf6c5e7/gr1.jpg

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