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A common polymorphism rs3781637 in MTNR1B is associated with type 2 diabetes and lipids levels in Han Chinese individuals

机译:MTNR1B中常见的多态性rs3781637与汉族人群2型糖尿病和血脂水平相关

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Background Several studies have shown that common variants in the MTNR1B gene were associated with fasting glucose level and type 2 diabetes. The purpose of this study was to examine whether tagging single nucleotide polymorphisms (SNPs) in the MTNR1B region were associated with type 2 diabetes and related traits in a Han Chinese population. Methods We investigated the association of polymorphisms in the MTNR1B gene with type 2 diabetes by employing a case-control study design (1118 cases and 1161 controls). Three tagging SNPs (rs10830963, rs3781637, and rs1562444) with R20.05 across the region of the MTNR1B gene were studied. Genotyping was performed by matrix-assisted laser desorption/ionization time-of-flight mass spectroscopy using a MassARRAY platform. Results The polymorphism rs3781637 was associated with type 2 diabetes adjusted for age, sex and body mass index (BMI) in the additive model and recessive model (OR = 1.22, 95% CI 1.01-1.46, p = 0.038 and OR = 2.81, 95% CI 1.28-6.17, p = 0.01, respectively). In the non-diabetic controls, rs3781637 was nominally associated with plasma triglyceride, total cholesterol and low density lipoprotein cholesterol (LDL-C) levels in the recessive model (p = 0.018, 0.008 and 0.038, respectively). After adjustment for multiple comparisons, the associations of rs3781637 with total cholesterol and LDL-C remained significant in the recessive model (the empirical p = 0.024 and 0.045, respectively), but the association between rs3781637 and triglyceride became non-significant (the empirical p = 0.095). The associations of rs10830963 and rs1562444 with type 2 diabetes and related traits were not significant in the additive, dominant and recessive models. Conclusions The rs3781637 A/G polymorphism of the MTNR1B gene is associated with type 2 diabetes, plasma, total cholesterol and LDL-C levels in the Han Chinese population.
机译:背景多项研究表明,MTNR1B基因的常见变异与空腹血糖水平和2型糖尿病有关。这项研究的目的是检查在中国汉族人群中MTNR1B区的单核苷酸多态性(SNPs)是否与2型糖尿病及其相关性状有关。方法我们采用病例对照研究设计(1118例和1161例对照),研究了MTNR1B基因多态性与2型糖尿病的相关性。研究了在MTNR1B基因区域内三个R 2 0.05的标记SNP(rs10830963,rs3781637和rs1562444)。基因分型是通过使用MassARRAY平台的基质辅助激光解吸/电离飞行时间质谱进行的。结果rs3781637基因多态性与在加性模型和隐性模型中经过年龄,性别和体重指数(BMI)调整的2型糖尿病相关(OR = 1.22,95%CI 1.01-1.46,p = 0.038和OR = 2.81,95 %CI 1.28-6.17,p = 0.01)。在非糖尿病对照组中,隐性模型中rs3781637与血浆甘油三酸酯,总胆固醇和低密度脂蛋白胆固醇(LDL-C)水平相关(分别为p = 0.018、0.008和0.038)。经过多次比较调整后,隐性模型中rs3781637与总胆固醇和LDL-C的关联仍然显着(经验p分别为0.024和0.045),但是rs3781637与甘油三酸酯之间的关联变得不显着(经验p = 0.095)。在加性,显性和隐性模型中,rs10830963和rs1562444与2型糖尿病及其相关性状的相关性均不显着。结论MTNR1B基因的rs3781637 A / G多态性与2型糖尿病,血浆,总胆固醇和LDL-C水平有关。

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