4.4 Review

Cardiac ion channels in health and disease

期刊

HEART RHYTHM
卷 7, 期 1, 页码 117-126

出版社

ELSEVIER SCIENCE INC
DOI: 10.1016/j.hrthm.2009.08.005

关键词

Action potential; Atrial fibrillation; Brugada syndrome; Current; Heart failure; Inherited arrhythmia; Ion channel; Long QT syndrome; Myocardial infarction

向作者/读者索取更多资源

Cardiac electrical activity depends on the coordinated propagation of excitatory stimuli through the heart and, as a consequence, the generation of action potentials in individual cardiomyocytes. Action potential formation results from the opening and closing (gating) of ion channels that are expressed within the sarcolemma of cardiomyocytes. Ion channels possess distinct genetic, molecular, pharmacologic, and gating properties and exhibit dissimilar expression levels within different cardiac regions. By gating, ion channels permit ion currents across the sarcolemma, thereby creating the different phases of the action potential ( e. g., resting phase, depolarization, repolarization). The importance of ion channels in maintaining normal heart rhythm is reflected by the increased incidence of arrhythmias in inherited diseases that are linked to mutations in genes encoding ion channels or their accessory proteins and in acquired diseases that are associated with changes in ion channel expression levels or gating properties. This review discusses ion channels that contribute to action potential formation in healthy hearts and their role in inherited and acquired diseases.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.4
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

Editorial Material Cardiac & Cardiovascular Systems

Genetic screening in acquired long QT syndrome? CAUTION: proceed carefully

Ahmad S. Amin, Arthur A. M. Wilde

EUROPEAN HEART JOURNAL (2016)

Letter Cardiac & Cardiovascular Systems

Letter by Amin et al Regarding Article, Genetic Modifiers for the Long-QT Syndrome: How Important Is the Role of Variants in the 3′ Untranslated Region of KCNQ1?

Ahmad S. Amin, Yigal M. Pinto, Michael J. Ackerman, Arthur A. M. Wilde

CIRCULATION-CARDIOVASCULAR GENETICS (2016)

Article Cardiac & Cardiovascular Systems

Prognostic significance of fever-induced Brugada syndrome

Yuka Mizusawa, Hiroshi Morita, Arnon Adler, Ofer Havakuk, Aurelie Thollet, Philippe Maury, Dao W. Wang, Kui Hong, Estelle Gandjbakhch, Frederic Sacher, Dan Hu, Ahmad S. Amin, Najim Lahrouchi, Hanno L. Tan, Charles Antzelevitch, Vincent Probst, Sami Viskin, Arthur A. M. Wilde

HEART RHYTHM (2016)

Letter Cardiac & Cardiovascular Systems

Letter by Amin et al Regarding Article, Genetic Modifiers for the Long-QT Syndrome: How Important Is the Role of Variants in the 3′ Untranslated Region of KCNQ1?

Ahmad S. Amin, Yigal M. Pinto, Michael J. Ackerman, Arthur A. M. Wilde

CIRCULATION-CARDIOVASCULAR GENETICS (2016)

Article Cardiac & Cardiovascular Systems

Channelopathies, genetic testing and risk stratification

Arthur A. M. Wilde, Ahmad Amin

INTERNATIONAL JOURNAL OF CARDIOLOGY (2017)

Article Cardiac & Cardiovascular Systems

RBM20 Mutations Induce an Arrhythmogenic Dilated Cardiomyopathy Related to Disturbed Calcium Handling

Maarten M. G. van den Hoogenhof, Abdelaziz Beqqali, Ahmad S. Amin, Ingeborg van der Made, Simona Aufiero, Mohsin A. F. Khan, Cees A. Schumacher, Joeri A. Jansweijer, Karin Y. van Spaendonck-Zwarts, Carol Ann Remme, Johannes Backs, Arie O. Verkerk, Antonius Baartscheer, Yigal M. Pinto, Esther E. Creemers

CIRCULATION (2018)

Editorial Material Cardiac & Cardiovascular Systems

The phenotype is equally important in promoting variants from benign to pathogenic as well as in demoting variants from pathogenic to benign

Ahmad S. Amin, Arthur A. M. Wilde

HEART RHYTHM (2018)

Article Cardiac & Cardiovascular Systems

SCN5A mutation type and topology are associated with the risk of ventricular arrhythmia by sodium channel blockers

Ahmad S. Amin, Yolan J. Reckman, Elena Arbelo, Anne M. Spanjaart, Pieter G. Postema, Rafik Tadros, Michael W. Tanck, Maarten P. Van den Berg, Arthur A. M. Wilde, Hanno L. Tan

INTERNATIONAL JOURNAL OF CARDIOLOGY (2018)

Article Cardiac & Cardiovascular Systems

Predicting cardiac electrical response to sodium-channel blockade and Brugada syndrome using polygenic risk scores

Rafik Tadros, Hanno L. Tan, Sulayman el Mathari, Jan A. Kors, Pieter G. Postema, Najim Lahrouchi, Leander Beekman, Milena Radivojkov-Blagojevic, Ahmad S. Amin, Thomas Meitinger, Michael W. Tanck, Arthur A. Wilde, Connie R. Bezzina

EUROPEAN HEART JOURNAL (2019)

Article Cardiac & Cardiovascular Systems

Sudden cardiac death in families with premature cardiovascular disease

Caroline Bruikman, Maurice W. J. de Ronde, Ahmed Amin, Sonja Levy, Pien Lof, Ursula de Ruijter, G. Kees Hovingh, Hanno L. Tan, Sara-Joan Pinto-Sietsma

Article Cardiac & Cardiovascular Systems

An International, Multicentered, Evidence-Based Reappraisal of Genes Reported to Cause Congenital Long QT Syndrome

Arnon Adler, Valeria Novelli, Ahmad S. Amin, Emanuela Abiusi, Melanie Care, Eline A. Nannenberg, Harriet Feilotter, Simona Amenta, Daniela Mazza, Hennie Bikker, Amy C. Sturm, John Garcia, Michael J. Ackerman, Raymond E. Hershberger, Marco V. Perez, Wojciech Zareba, James S. Ware, Arthur A. M. Wilde, Michael H. Gollob

CIRCULATION (2020)

Review Cardiac & Cardiovascular Systems

Disease Modifiers of Inherited SCN5A Channelopathy

Arie O. Verkerk, Ahmad S. Amin, Carol Ann Remme

FRONTIERS IN CARDIOVASCULAR MEDICINE (2018)

Review Cardiac & Cardiovascular Systems

Clinical Spectrum of SCN5A Mutations Long QT Syndrome, Brugada Syndrome, and Cardiomyopathy

Arthur A. M. Wilde, Ahmad S. Amin

JACC-CLINICAL ELECTROPHYSIOLOGY (2018)

Review Cardiac & Cardiovascular Systems

The future of sudden cardiac death research

Ahmad S. Amin, Arthur A. M. Wilde

PROGRESS IN PEDIATRIC CARDIOLOGY (2017)

暂无数据