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遗传性通道病中的心房颤动。

Atrial Fibrillation in Inherited Channelopathies.

机构信息

Division of Cardiology, Department of Medicine, University of Illinois at Chicago, 820 S Wood Street, Suite 920S, Chicago, IL 60612, USA; Division of Cardiology, Department of Pharmacology, University of Illinois at Chicago, 820 S Wood Street, Suite 920S, Chicago, IL 60612, USA.

Division of Cardiology, Department of Medicine, University of Illinois at Chicago, 820 S Wood Street, Suite 920S, Chicago, IL 60612, USA; Division of Cardiology, Department of Pharmacology, University of Illinois at Chicago, 820 S Wood Street, Suite 920S, Chicago, IL 60612, USA; Department of Medicine, Jesse Brown Veterans Administration, 820 S Wood Street, Suite 920S, Chicago, IL 60612, USA.

出版信息

Card Electrophysiol Clin. 2021 Mar;13(1):155-163. doi: 10.1016/j.ccep.2020.10.004. Epub 2021 Jan 8.

DOI:10.1016/j.ccep.2020.10.004
PMID:33516393
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9172630/
Abstract

Atrial fibrillation (AF), the common sustained arrhythmia in clinical practice, has major public health implications due to its associated morbidity and increased mortality. The AF epidemic is due to the burgeoning elderly population and the identification of novel risk factors, for example, genetics. Since the diagnosis of AF has a major impact on the clinical assessment and management of patients with inherited arrhythmia syndromes, improved understanding of the cause and pathogenesis of AF has provided important insights into the underlying pathophysiological mechanisms of this common arrhythmia and identified potential mechanism-based therapies.

摘要

心房颤动(AF)是临床实践中常见的持续性心律失常,由于其相关的发病率和死亡率增加,具有重大的公共卫生意义。AF 流行是由于老年人口的增加和新的危险因素的出现,例如遗传因素。由于 AF 的诊断对遗传性心律失常综合征患者的临床评估和治疗有重大影响,因此,对 AF 病因和发病机制的深入了解为这种常见心律失常的潜在病理生理机制提供了重要的见解,并确定了潜在的基于机制的治疗方法。

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Atrial Fibrillation in Inherited Channelopathies.遗传性通道病中的心房颤动。
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Electrocardiographic Changes Associated with Early Repolarization Pattern in Healthy Young Males.健康年轻男性早期复极综合征与心电图改变。

本文引用的文献

1
Differences in Epidemiology and Risk Factors for Atrial Fibrillation Between Women and Men.女性与男性心房颤动的流行病学及危险因素差异。
Front Cardiovasc Med. 2020 Jan 31;7:3. doi: 10.3389/fcvm.2020.00003. eCollection 2020.
2
Differences in Short QT Syndrome Subtypes: A Systematic Literature Review and Pooled Analysis.短QT综合征亚型的差异:系统文献综述与汇总分析
Front Genet. 2020 Jan 17;10:1312. doi: 10.3389/fgene.2019.01312. eCollection 2019.
3
The many faces of early repolarization syndrome: A single-center case series.
Medicina (Kaunas). 2022 Aug 4;58(8):1048. doi: 10.3390/medicina58081048.
早期复极综合征的多种表现形式:单中心病例系列。
Heart Rhythm. 2020 Feb;17(2):273-281. doi: 10.1016/j.hrthm.2019.09.013. Epub 2019 Sep 12.
4
Atrial fibrillation and risk of major arrhythmic events in Brugada syndrome: A meta-analysis. Brugada综合征中的心房颤动与主要心律失常事件风险:一项荟萃分析。
Ann Noninvasive Electrocardiol. 2019 Nov;24(6):e12676. doi: 10.1111/anec.12676. Epub 2019 Jul 29.
5
Ablation of atrial fibrillation in patients with Brugada syndrome: A systematic review of the literature.Brugada综合征患者心房颤动的消融治疗:文献系统评价
J Arrhythm. 2018 Sep 3;35(1):18-24. doi: 10.1002/joa3.12113. eCollection 2019 Feb.
6
Early repolarization and risk of lone atrial fibrillation.早期复极与孤立性心房颤动风险。
J Cardiovasc Electrophysiol. 2019 Apr;30(4):565-568. doi: 10.1111/jce.13848. Epub 2019 Jan 25.
7
Abnormally high risk of stroke in Brugada syndrome.Brugada 综合征患者发生中风的风险异常高。
J Cardiovasc Med (Hagerstown). 2019 Feb;20(2):59-65. doi: 10.2459/JCM.0000000000000723.
8
Multi-ethnic genome-wide association study for atrial fibrillation.多民族全基因组关联研究心房颤动。
Nat Genet. 2018 Jun 11;50(9):1225-1233. doi: 10.1038/s41588-018-0133-9.
9
Dysfunctional Nav1.5 channels due to SCN5A mutations.功能失调的 Nav1.5 通道由于 SCN5A 突变。
Exp Biol Med (Maywood). 2018 Jun;243(10):852-863. doi: 10.1177/1535370218777972. Epub 2018 May 27.
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Hydroquinidine Prevents Life-Threatening Arrhythmic Events in Patients With Short QT Syndrome.氢奎尼丁可预防短 QT 综合征患者发生危及生命的心律失常事件。
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