Susceptibility genes and modifiers for cardiac arrhythmias.

Abstract:

:The last decade has seen a dramatic increase in the understanding of the molecular basis of arrhythmias. Much of this new information has been driven by genetic studies that focused on rare, monogenic arrhythmia syndromes that were accompanied or followed by cellular electrophysiological or biochemical studies. The marked clinical heterogeneity known from these familial arrhythmia syndromes has led to the development of a multifactorial ("multi-hit") concept of arrhythmogenesis in which causal gene mutations have a major effect on disease expression that is further modified by other factors such as age, gender, sympathetic tone, and environmental triggers. Systematic genetic studies have unraveled an unexpected DNA sequence variance in these arrhythmia genes that has ethnic-specific patterns. Whether this genetic variance may contribute as a second genetic modifier for arrhythmia development is under current investigation. The aim of this article is to review common genetic variation in ion channel genes and to compare these recent findings.

journal_name

Cardiovasc Res

journal_title

Cardiovascular research

authors

Kääb S,Schulze-Bahr E

doi

10.1016/j.cardiores.2005.04.005

subject

Has Abstract

pub_date

2005-08-15 00:00:00

pages

397-413

issue

3

eissn

0008-6363

issn

1755-3245

pii

S0008-6363(05)00180-X

journal_volume

67

pub_type

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