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01-11-2014 | Short Communication

Association of common variants in NOS1AP gene with sudden unexplained nocturnal death syndrome in the southern Chinese Han population

Authors: Lei Huang, Yangeng Yu, Yili Chen, David J. Tester, Shuangbo Tang, Michael J. Ackerman, Zichuang Yuan, Jianding Cheng

Published in: International Journal of Legal Medicine | Issue 6/2014

Abstract

Here, we investigate the association of common polymorphisms of the NOS1AP gene with sudden unexplained nocturnal death syndrome (SUNDS) in the southern Chinese Han population. We genetically screened five common NOS1AP polymorphisms (rs10918594, rs12143842, rs16847548, rs12567209, and rs10494366) previously reported to be associated with QT interval variation and sudden cardiac death (SCD) in 123 sporadic SUNDS cases and 166 healthy controls using polymerase chain reaction (PCR) and direct DNA sequencing. In the present study, the A allele of rs12567209 was more common in controls than in SUNDS cases, which was associated with 0.656-fold decreased risk of SUNDS (95 % confidence interval 0.431 to 0.998, P = 0.048) compared with G allele. Under the dominant genetic model, GA + AA genotype of rs12567209 was also more common in controls than in SUNDS cases, which was associated with 0.604-fold decreased risk of SUNDS (95 % confidence interval 0.368 to 0.991, P = 0.045) compared with GG genotype. No significant associations of rs10918594, rs12143842, rs16847548, and rs10494366 with SUNDS were observed (P > 0.05). In haplotype analyses, the distribution of haplotype GCTA was significantly overrepresented in controls compared to SUNDS cases (P = 0.040). This is the first report of the association of common NOS1AP polymorphisms with SUNDS in the southern Chinese Han population. These findings suggest that the A allele of rs12567209 and haplotype GCTA may serve as a protective modifier.

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Title: Association of common variants in NOS1AP gene with sudden unexplained nocturnal death syndrome in the southern Chinese Han population
Authors: Lei Huang
Yangeng Yu
Yili Chen
David J. Tester
Shuangbo Tang
Michael J. Ackerman
Zichuang Yuan
Jianding Cheng
Publication date: 01-11-2014
Publisher: Springer Berlin Heidelberg
Published in: International Journal of Legal Medicine / Issue 6/2014
Print ISSN: 0937-9827
Electronic ISSN: 1437-1596
DOI: https://doi.org/10.1007/s00414-014-0973-5

At a glance: The STEP trials

Springer Medicine

Association of common variants in NOS1AP gene with sudden unexplained nocturnal death syndrome in the southern Chinese Han population

Abstract

At a glance: The STEP trials

Springer Medicine

Abstract

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