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Circulation. 2009 Oct 27;120(17):1657-63. doi: 10.1161/CIRCULATIONAHA.109.879643. Epub 2009 Oct 12.

NOS1AP is a genetic modifier of the long-QT syndrome.

Author information

1
Department of Lung, Blood, and Heart, University of Pavia, Pavia, Italy.

Abstract

BACKGROUND:

In congenital long-QT syndrome (LQTS), a genetically heterogeneous disorder that predisposes to sudden cardiac death, genetic factors other than the primary mutation may modify the probability of life-threatening events. Recent evidence indicates that common variants in NOS1AP are associated with the QT-interval duration in the general population.

METHODS AND RESULTS:

We tested the hypothesis that common variants in NOS1AP modify the risk of clinical manifestations and the degree of QT-interval prolongation in a South African LQTS population (500 subjects, 205 mutation carriers) segregating a founder mutation in KCNQ1 (A341V) using a family-based association analysis. NOS1AP variants were significantly associated with the occurrence of symptoms (rs4657139, P=0.019; rs16847548, P=0.003), with clinical severity, as manifested by a greater probability for cardiac arrest and sudden death (rs4657139, P=0.028; rs16847548, P=0.014), and with greater likelihood of having a QT interval in the top 40% of values among all mutation carriers (rs4657139, P=0.03; rs16847548, P=0.03).

CONCLUSIONS:

These findings indicate that NOS1AP, a gene first identified as affecting the QTc interval in a general population, also influences sudden death risk in subjects with LQTS. The association of NOS1AP genetic variants with risk for life-threatening arrhythmias suggests that this gene is a genetic modifier of LQTS, and this knowledge may be clinically useful for risk stratification for patients with this disease, after validation in other LQTS populations.

PMID:
19822806
PMCID:
PMC2783481
DOI:
10.1161/CIRCULATIONAHA.109.879643
[Indexed for MEDLINE]
Free PMC Article

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