Complex inheritance for susceptibility to sudden cardiac death

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Abstract

Sudden cardiac death (SCD) from ventricular fibrillation during myocardial infarction is a leading cause of total and cardiovascular mortality. It has a multifactorial, complex nature and aggregates in families, implicating the involvement of heritable factors in the determination of risk. During the last few years, genome-wide association studies have uncovered common genetic variants modulating risk of SCD. We here review the current insight on genetic determinants of SCD in the community and describe the genome-wide association approaches undertaken thus far in uncovering genetic determinants of SCD risk
Original languageEnglish
Pages (from-to)6864-6872
JournalCurrent pharmaceutical design
Volume19
Issue number39
DOIs
Publication statusPublished - 2013

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