Schulze-Bahr Eric
Leibniz Institute for Arteriosclerosis Research (LIFA), Molecular Cardiology, University of Münster, Germany.
Prog Biophys Mol Biol. 2008 Oct-Nov;98(2-3):289-300. doi: 10.1016/j.pbiomolbio.2009.01.008. Epub 2009 Jan 29.
Cardiac arrhythmias in the absence of structural heart diseases can be subdivided in those cases which are acquired and those which are linked to genetic defects on cardiac ion channels and regulatory subunits. Although acquired arrhythmias do not contain any obviously genetic component the observation of frequently occurring single nucleotide polymorphism (SNPs) identified in cardiac ion channel genes lead to the question if these natural variants can influence the development of acquired forms of cardiac arrhythmias and thus serve as genetic susceptibility markers. This review summarizes the results of genetic association and linkage studies in drug induced long-QT syndrome and atrial and ventricular fibrillation and discusses advantages and future directions of this topic in cardiac research.
无结构性心脏病的心律失常可细分为获得性病例和与心脏离子通道及调节亚基基因缺陷相关的病例。尽管获得性心律失常不包含任何明显的遗传成分,但在心脏离子通道基因中发现的频繁出现的单核苷酸多态性(SNP)引发了一个问题,即这些自然变异是否会影响获得性心律失常的发生发展,从而作为遗传易感性标志物。本文综述了药物性长QT综合征、心房颤动和心室颤动的遗传关联和连锁研究结果,并讨论了该主题在心脏研究中的优势和未来方向。