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首页> 外文期刊>Zeitschrift fur Arznei- und Gewurzpflanzen >Lack of association between FTO gene variations and metabolic healthy obese (MHO) phenotype: Tehran Cardio-metabolic Genetic Study (TCGS)
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Lack of association between FTO gene variations and metabolic healthy obese (MHO) phenotype: Tehran Cardio-metabolic Genetic Study (TCGS)

机译:FTO基因变异和代谢健康肥胖(MHO)表型之间缺乏关联:德黑兰心脏代谢遗传学研究(TCGS)

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Background Obesity is currently an international epidemic and metabolic derangements pose these individuals at greater risk for future morbidity and mortality. Genetics and environmental factors have undeniable effects and among genetic risk factors, FTO/CETP genes are important. The current study examines the interaction between obesity phenotypes and FTO/CETP SNPs and their effects on lipid profile changes. Materials and methods We selected 954 adult subjects from TCGS (47.9% male). Participants were stratified according to their BMI and presence of metabolic syndrome according to the Joint Interim Statement (JIS) definition. Nine selected polymorphisms from FTO/CETP genes were genotyped using Tetra ARMS-PCR method. After age and sex adjustment the interaction of 9 markers with lipid profiles among phenotypes were tested by PASW. Results In three main groups, HDL_C level had a strong significant association with CETP markers: (rs3764261, beta(95% CI) - 0.48(- 0.61 to - 0.35), P = 1.0 x 10(-11)), (rs1800775, beta(95% CI) 0.5(0.36;0.65), P = 1.0 x 10(-6)) and (rs1864163, beta(95% CI) 0.3(0.16;0.43), P = 9.1 x 10(-5)). This association was also seen in rs7202116 within the total population. In only unhealthy metabolic obese (MUHO) subgroups four new FTO markers (rs1421085, rs1121980, rs1558902 and rs8050136) (P value < 0.01) demonstrated significant association, even after lipid profile adjustment. Conclusion In the present study, we investigated the association between obesity phenotypes and some variations in FTO/CETP genes for the first time. Our study showed that four markers in the first intron of the FTO gene should be the risk marker in MUHO participants.
机译:背景技术肥胖目前是一个国际疫情和代谢紊乱使这些人具有更大的风险,以满足未来的发病率和死亡率。遗传和环境因素具有不可否认的影响和遗传危险因素,FTO / CETP基因很重要。目前的研究检查了肥胖表型和FTO / CETP SNP之间的相互作用及其对脂质曲线变化的影响。材料和方法我们选择了来自TCG的954名成年人(男性47.9%)。根据其BMI(JIS)定义,根据其BMI和代谢综合征的存在,参与者分层。来自FTO / CETP基因的九种选定多态性使用Tetra Arms-PCR方法进行基因分型。年龄和性调整后,通过PASW测试表型中具有脂质谱的9个标记的相互作用。结果三个主要群体,HDL_C水平与CETP标记有着强烈的显着关系:(RS3764261,β(95%CI) - 0.48( - 0.61至-0.35),P = 1.0 x 10(-11)),(RS1800775, β(95%CI)0.5(0.36; 0.65),P = 1.0×10(-6))和(RS1864163,β(95%CI)0.3(0.16; 0.43),P = 9.1 x 10(-5)) 。该协会在总人口中的RS7202116中也见过。在只有不健康的代谢肥胖(MUHO)亚组四个新的FTO标记(RS1421085,RS1121980,RS1558902和RS8050136)(P值<0.01)也表现出显着的关联,即使在脂质剖面调节之后。结论在本研究中,我们首次研究了肥胖表型与FTO / CETP基因的一些变化之间的关联。我们的研究表明,FTO基因的第一个内含子中的四个标记应该是Muho参与者的风险标志。

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