Arrhythmias and Conduction Disturbances in Autoimmune Rheumatic Disorders.

IF 2.6 Q2 CARDIAC & CARDIOVASCULAR SYSTEMS Arrhythmia & Electrophysiology Review Pub Date : 2021-04-01 DOI:10.15420/aer.2020.43
Sotiris C Plastiras, Haralampos M Moutsopoulos
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引用次数: 9

Abstract

Rhythm and conduction disturbances and sudden cardiac death are important manifestations of cardiac involvement in autoimmune rheumatic diseases (ARD), which have a serious impact on morbidity and mortality. While the underlying arrhythmogenic mechanisms are multifactorial, myocardial fibrosis plays a pivotal role. It accounts for a substantial portion of cardiac mortality and may manifest as atrial and ventricular arrhythmias, conduction system abnormalities, biventricular cardiac failure or sudden death. In patients with ARD, myocardial fibrosis is considered to be the hallmark of cardiac involvement as a result of inflammatory process or to coronary artery occlusive disease. Myocardial fibrosis constitutes the pathological substrates for reentrant circuits. The presence of supraventricular extra systoles, tachyarrhythmias, ventricular activity and conduction disturbances are not uncommon in patients with ARDs, more often in systemic lupus erythematosus, systemic sclerosis, rheumatoid arthritis, inflammatory muscle disorders and anti-neutrophil cytoplasm antibody-associated vasculitis. In this review, the type, the relative prevalence and the underlying mechanisms of rhythm and conduction disturbances in the emerging field of cardiorheumatology are provided.

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自身免疫性风湿病的心律失常和传导障碍。
心律传导障碍和心源性猝死是自身免疫性风湿性疾病(ARD)心脏受累的重要表现,严重影响发病率和死亡率。虽然潜在的心律失常机制是多因素的,但心肌纤维化起着关键作用。它占心脏死亡率的很大一部分,可能表现为心房和室性心律失常,传导系统异常,双室心力衰竭或猝死。在ARD患者中,心肌纤维化被认为是由炎症过程或冠状动脉闭塞性疾病引起的心脏受累的标志。心肌纤维化构成可重入回路的病理底物。在ARDs患者中,室上室外收缩、心动过速、心室活动和传导障碍并不少见,更常见于系统性红斑狼疮、系统性硬化症、类风湿关节炎、炎性肌肉疾病和抗中性粒细胞细胞质抗体相关血管炎。本文综述了心律和传导障碍的类型、相对患病率和潜在的机制,在心血管病学的新兴领域。
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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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