Key result
Homozygosity for the SCN5A S1103Y mutation in African American infants was associated with a 24-fold increase in the risk of sudden infant death syndrome compared with controls.
Why the study?
Does the SCN5A S1103Y polymorphism increase the risk of SIDS under acidic environmental conditions?
Does the SCN5A S1103Y polymorphism increase the risk of SIDS under acidic environmental conditions?
Effect estimate: 24-fold increase in risk
The SCN5A S1103Y polymorphism significantly increases the risk of SIDS in African Americans, with in vitro evidence demonstrating that acidosis triggers arrhythmogenic late sodium current reopenings.
In this issue of the JCI, Bowers et al. show that the common polymorphism of the cardiac voltage-gated sodium channel, type Valpha (SCN5A), designated S1103Y, found in African Americans is associated with an increased risk of sudden infant death syndrome (SIDS). Wild-type and mutant SCN5A channels both functioned typically under normal conditions in vitro, but exposure to acidic intracellular pH levels such as those found in respiratory acidosis--a known risk factor for SIDS--produced abnormal gain-of-function late reopenings of S1103Y channels, behavior that is often associated with cardiac arrhythmias. These pathologic late reopenings were suppressed by low levels of the channel-blocking drug mexiletine. These findings provide an excellent illustration of a causal relationship between the interaction of the environment and genetic background in SIDS and also raise interesting questions about the linkage of a genetic abnormality with a clinical phenotype.
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J. C. Makielski (2006) conducted an editorial in Sudden infant death syndrome (SIDS) (n=224). SCN5A polymorphism S1103Y homozygosity vs. Controls was evaluated on Risk of sudden infant death syndrome (SIDS) (24-fold increase in risk). Homozygosity for the SCN5A S1103Y mutation in African American infants was associated with a 24-fold increase in the risk of sudden infant death syndrome compared with controls.
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