HHEX gene polymorphisms are associated with type 2 diabetes in the Dutch Breda cohort

作者: Jana V van Vliet-Ostaptchouk , N Charlotte Onland-Moret , Timon W van Haeften , Lude Franke , Clara C Elbers

DOI: 10.1038/SJ.EJHG.5202008

关键词:

摘要: Recently, the hematopoietically expressed homeobox (HHEX) gene, encoding a transcription factor, was identified in large genome-wide scan French individuals as type 2 diabetes (T2D)-susceptibility locus. We aimed to check whether this finding could be replicated Dutch T2D cohort. Two common variants (rs7923837 and rs1111875) located near HHEX gene were genotyped 501 unrelated patients 920 healthy controls. The major alleles of both overrepresented cases compared with controls (66.7 vs 64.1%, P=0.16 for rs7923837 64.6 60.4%, P=0.027 rs1111875). For polymorphisms, risk significantly increased carriers (rs7923837: odds ratio (OR): 1.57, 95% confidence interval (CI): 1.08-2.27, P=0.017 rs1111875: OR: 1.68, CI: 1.19-2.35, P=0.003). haplotype analysis did not reveal that provided stronger evidence association than each variant individually. Assuming dominant genetic model, population-attributable risks due at-risk rs1111875 estimated 33 36%, respectively. These data provide contribute population.

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