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Polymorphisms in TCF7L2 gene are associated with gestational diabetes mellitus in Chinese Han population.


ABSTRACT: This study aimed to investigate the possible association between diabetes susceptibility gene transcription factor 7-like 2 (TCF7L2) and gestational diabetes mellitus (GDM) in a Chinese Han population. A total of 556 GDM patients and 500 Non-GDM were included. Eighteen single nucleotide polymorphisms (SNPs) were evaluated. Fifteen tag SNPs were selected from HapMap CHB database with a minor allele frequency of >0.2 and r(2) of >0.8. Three additional SNPs were also chosen because these SNPs are associated with type 2 diabetes in East Asians. TCF7L2 rs290487, rs6585194, and rs7094463 polymorphisms were found to be significantly associated with GDM. In multivariate analysis, rs290487 genetic variation (OR?=?2.686 per each C allele, P?=?0.002), pre-BMI?>?24?kg/m(2) (OR?=?1.592, P?=?0.018), age?>?25 years (OR?=?1.780, P?=?0.012) and LDL-C?>?3.6?mmol/L (OR?=?2.034, P?=?0.009) were identified as independent risk factors of GDM, rs7094463 genetic variation (OR?=?0.429 per each G allele, P?=?0.005) was identified as independent protect factor of GDM. This finding suggests that TCF7L2 rs290487, and rs7094463 were a potential clinical value for the prediction of GDM.

SUBMITTER: Ye D 

PROVIDER: S-EPMC4964615 | biostudies-literature | 2016 Jul

REPOSITORIES: biostudies-literature

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Polymorphisms in TCF7L2 gene are associated with gestational diabetes mellitus in Chinese Han population.

Ye Dan D   Fei Yang Y   Ling Qi Q   Xu Weiwei W   Zhang Zhe Z   Shu Jing J   Li Chengjiang C   Dong Fengqin F  

Scientific reports 20160728


This study aimed to investigate the possible association between diabetes susceptibility gene transcription factor 7-like 2 (TCF7L2) and gestational diabetes mellitus (GDM) in a Chinese Han population. A total of 556 GDM patients and 500 Non-GDM were included. Eighteen single nucleotide polymorphisms (SNPs) were evaluated. Fifteen tag SNPs were selected from HapMap CHB database with a minor allele frequency of >0.2 and r(2) of >0.8. Three additional SNPs were also chosen because these SNPs are a  ...[more]

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