Sudden infant death syndrome: how significant are the cardiac channelopathies?

Abstract:

:Having an apparently healthy, thriving infant fail to reach his/her first birthday is profoundly tragic. This tragedy is compounded when the infant's death is unexpected and unexplained, signed out as sudden infant death syndrome (SIDS). Despite impressive success and welcome reductions in these tragic deaths due in large measure to "Back-to-Sleep" campaigns, the fundamental pathogenic mechanisms precipitating such deaths remain dimly exposed. Here, we review the causal link between SIDS and mutations involving the SCN5A-encoded cardiac sodium channel, provide new findings following extensive postmortem genetic testing of long QT syndrome (LQTS)-associated potassium channel genes in a population-based cohort of SIDS, and summarize the current understanding regarding the spectrum and prevalence of cardiac channelopathies in the pathogenesis of SIDS.

journal_name

Cardiovasc Res

journal_title

Cardiovascular research

authors

Tester DJ,Ackerman MJ

doi

10.1016/j.cardiores.2005.02.013

subject

Has Abstract

pub_date

2005-08-15 00:00:00

pages

388-96

issue

3

eissn

0008-6363

issn

1755-3245

pii

S0008-6363(05)00119-7

journal_volume

67

pub_type

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