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首页> 外文期刊>Diabetes, metabolic syndrome and obesity: targets and therapy >Identification of Genetic Variants for Female Obesity and Evaluation of the Causal Role of Genetically Defined Obesity in Polycystic Ovarian Syndrome
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Identification of Genetic Variants for Female Obesity and Evaluation of the Causal Role of Genetically Defined Obesity in Polycystic Ovarian Syndrome

机译:鉴定遗传变异性的女性肥胖与评价遗传定义肥胖在多囊卵巢综合征中的因果作用

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Purpose:Observational studies have demonstrated an increased risk of polycystic ovarian syndrome (PCOS) in obese women. This study aimed to identify genetic variants influencing obesity in females and to evaluate the causal association between genetically defined obesity and PCOS in Korean women.Methods:Two-stage GWAS was conducted to identify genetic variants influencing obesity traits (such as body mass index [BMI], waist-hip ratio [WHR], and waist circumference [WC]) in Korean women. Two-sample Mendelian randomization (MR) analysis was employed to evaluate the causal effect of variants as genetic instruments for female obesity on PCOS.Results:Meta-analysis of 9953 females combining discovery (N = 4658) and replication (N = 5295) stages detected four (rs11162584, rs6760543, rs828104, rs56137030), six (rs139702234, rs2341967, rs73059848, rs5020945, rs550532151, rs61971548), and two genetic variants (rs7722169, rs7206790) suggesting a highly significant association (P 1×10 -6 ) with BMI, WHR, and WC, respectively. Of these, an intron variant rs56137030 in FTO achieved genome-wide significant association (P = 3.39×10 -8 ) with BMI in females. Using variants for female obesity, their effect on PCOS in 946 cases and 976 controls was evaluated by MR analysis. MR results indicated no significant association between genetically defined obesity and PCOS in Korean women.Conclusion:This study, for the first time, revealed genetic variants for female obesity in the Korean population and reported no causal association between genetically defined obesity and PCOS in Korean women.? 2020 Ahn et al.
机译:目的:观察性研究表明,肥胖女性的多囊卵巢综合征(PCOS)的风险增加。本研究旨在识别影响雌性肥胖的遗传变异,并评估韩国女性的遗传定义肥胖和PCO之间的因果关系。方法:进行两级GWA,以鉴定影响肥胖性状的遗传变异(如体重指数[BMI韩国女性的腰臀比[WHR]和腰围[WC])。使用两种样本的孟德尔随机化(MR)分析来评估变体作为PCOS女性肥胖遗传仪器的因果效果。结果:9953女性的Meta分析结合发现(n = 4658)和复制(n = 5295)阶段检测到四(RS11162584,RS6760543,RS828104,RS56137030),六(RS139702234,RS2341967,RS73059848,RS5197125,RS550532151,RS61971548)和两个遗传变体(RS7722169,RS7206790),表明高度重要的关联(P <1×10 -6)与BMI,WHR和WC分别。其中,在FTO中的内含子变异RS56137030在女性中使用BMI实现了基因组 - 宽的显着关联(P = 3.39×10 -8)。利用血液肥胖的变体,通过MR分析评估了946例患者对PCOS和976种对照的影响。结果表明,韩国女性的遗传定义肥胖和PCO之间没有显着关联。结论:本研究首次揭示了韩国人口中女性肥胖的遗传变异,并报告了韩国女性的遗传定义肥胖和PCO之间没有因果关系。? 2020 Ahn等人。

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