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A common variant of NOS1AP is associated with QT interval duration in a Chinese population with Type 2 diabetes
Author(s) -
Lu J.,
Hu C.,
Hu W.,
Zhang R.,
Wang C.,
Qin W.,
Yu W.,
Xiang K.,
Jia W.
Publication year - 2010
Publication title -
diabetic medicine
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.474
H-Index - 145
eISSN - 1464-5491
pISSN - 0742-3071
DOI - 10.1111/j.1464-5491.2010.03072.x
Subject(s) - qt interval , medicine , single nucleotide polymorphism , diabetes mellitus , type 2 diabetes , sudden cardiac death , population , cardiology , type 1 diabetes , genotype , endocrinology , genetics , biology , environmental health , gene
Diabet. Med. 27, 1074–1079 (2010) Abstract Aims Electrocardiographic ventricular repolarization QT parameters are independent risk factors for cardiovascular events and sudden cardiac death in diabetic patients. The aim of the study was to investigate the association of polymorphisms of the nitric oxide synthase 1 adaptor protein (NOS1AP) gene with QT interval in Chinese subjects with or without Type 2 diabetes. Methods Three single nucleotide polymorphisms (SNPs) (rs10494366, rs12143842 and rs12029454) were genotyped in 1240 Type 2 diabetic patients (631 men and 609 women) and 1196 normal controls (433 men and 763 women). Individuals with overt diseases other than diabetes were excluded. Heart‐rate corrected QT interval (QTc) was determined by standard 12‐lead ECG and Bazett formula. Sex‐pooled analysis and sex‐specific analysis for genotype–phenotype association were both conducted. Results In the diabetic group, the rs12143842 T allele was associated with a 3.87‐ms ( P = 0.014, empirical P = 0.039) increase in QTc duration for each additional allele copy, while rs10494366 and rs12029454 exhibited no significant association with QTc. We found no evidence of association for the three SNPs in subjects with normal glucose regulation. No significant SNP‐gender and ‐diabetes affection interaction was observed. Conclusions The genetic variant rs12143842 in NOS1AP is associated with QT interval duration in a Chinese population with Type 2 diabetes. Future studies in different populations are needed to validate this finding and to evaluate the impact of NOS1AP variants on cardiovascular events and sudden cardiac death in diabetic patients.