Genetic Polymorphisms as Risk Stratification Tool in Primary Preventive ICD Therapy.

ISRN cardiology Pub Date : 2011-01-01 Epub Date: 2011-04-18 DOI:10.5402/2011/457247
Roman Laszlo, Mathias C Busch, Jüergen Schreieck
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引用次数: 1

Abstract

More and more implantable cardioverter-defibrillators (ICDs) are implanted as primary prevention of sudden cardiac death (SCD). However, major problem in practice is to identify high-risk patients for SCD. Different methods for noninvasive risk stratification do not have a sufficient positive or negative predictive value. Since current approaches lead to implantation of ICDs in a large number of patients who will never suffer an arrhythmic event and simultaneously patients still die of SCD who currently did not seem eligible for primary preventive ICD implantation, there is a need for additional tools for risk stratification. Epidemiological studies point to a hereditary risk of SCD. Different susceptibility of each person concerning arrhythmogenic events might be explained by genetic polymorphisms. By obtaining an individual "pattern" of polymorphisms of genes encoding for proteins which are important in arrhythmogenesis in one patient, risk stratification in primary prevention of SCD might by improved.

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遗传多态性作为初级预防ICD治疗的风险分层工具。
植入式心律转复除颤器(ICDs)作为心脏性猝死(SCD)的一级预防手段被越来越多地植入。然而,在实践中主要的问题是识别SCD的高危患者。不同的无创风险分层方法没有足够的阳性或阴性预测值。由于目前的方法导致大量从未发生过心律失常事件的患者植入ICD,同时仍有患者死于SCD,目前似乎不符合初级预防性ICD植入的条件,因此需要额外的风险分层工具。流行病学研究指出SCD有遗传风险。每个人对心律失常事件的不同易感性可以用遗传多态性来解释。通过获得单个患者心律失常发生中重要的蛋白质编码基因多态性的个体“模式”,可以改善SCD一级预防的风险分层。
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