房颤患者底物、遗传学和危险因素评估的考虑。

IF 2.6 Q2 CARDIAC & CARDIOVASCULAR SYSTEMS Arrhythmia & Electrophysiology Review Pub Date : 2021-10-01 DOI:10.15420/aer.2020.51
Dominik Linz, Sander Verheule, Aaron Isaacs, Ulrich Schotten
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引用次数: 1

摘要

关注心房心律失常发生机制的研究成果的成功转化有可能为房颤患者提供量身定制的分类机制,并支持个性化的治疗方法。新的诊断技术和治疗策略的临床吸收和临床实施需要不同水平的转化研究方法。诊断翻译涉及临床诊断工具的开发。此外,需要多学科团队进行协作翻译,以描述遗传机制、分子途径、电生理特征和伴随的风险因素。本文综述了目前房颤底物表征、房颤潜在相关基因分析和房颤危险因素评估的方法。作者讨论了临床翻译和实施到临床实践中的挑战和障碍。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Considerations for the Assessment of Substrates, Genetics and Risk Factors in Patients with Atrial Fibrillation.

Successful translation of research focussing on atrial arrhythmogenic mechanisms has potential to provide a mechanism-tailored classification and to support personalised treatment approaches in patients with AF. The clinical uptake and clinical implementation of new diagnostic techniques and treatment strategies require translational research approaches on various levels. Diagnostic translation involves the development of clinical diagnostic tools. Additionally, multidisciplinary teams are required for collaborative translation to describe genetic mechanisms, molecular pathways, electrophysiological characteristics and concomitant risk factors. In this article, current approaches for AF substrate characterisation, analysis of genes potentially involved in AF and strategies for AF risk factor assessment are summarised. The authors discuss challenges and obstacles to clinical translation and implementation into clinical practice.

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来源期刊
Arrhythmia & Electrophysiology Review
Arrhythmia & Electrophysiology Review CARDIAC & CARDIOVASCULAR SYSTEMS-
CiteScore
5.10
自引率
6.70%
发文量
22
审稿时长
7 weeks
期刊最新文献
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