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Applicability of Obesity-Related SNPs and Their Effect Size Measures Defined on Populations with European Ancestry for Genetic Risk Estimation among Roma

机译:肥胖相关的SNP的适用性及其对欧洲祖先群体群体群体群体中群体的兴奋措施

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摘要

Investigations on the impact of genetic factors on the development of obesity have been limited regarding the Roma population—the largest and most vulnerable ethnic minority in Europe of Asian origin. Genetic variants identified from genetic association studies are primarily from European populations. With that in mind, we investigated the applicability of data on selected obesity-related single nucleotide polymorphisms (SNPs), obtained from the Hungarian general (HG) population of European origin, on the Hungarian Roma (HR) population. Twenty preselected SNPs in susceptible alleles, known to be significantly associated with obesity-related phenotypes, were used to estimate the effect of these SNPs on body mass index (BMI) and waist circumference (WC) in HG (N = 1783) and HR (N = 1225) populations. Single SNP associations were tested using linear and logistic regression models, adjusted for known covariates. Out of 20 SNPs, four located in FTO (rs1121980, rs1558902, rs9939609, and rs9941349) showed strong association with BMI and WC as continuous variables in both samples. Computations based on Adult Treatment Panel III (ATPIII) and the International Diabetes Federation’s (IDF) European and Asian criteria showed rs9941349 in FTO to be associated only with WC among both populations, and two SNPs (rs2867125, rs6548238) in TMEM18 associated with WC only in HG population. A substantial difference (both in direction and effect size) was observed only in the case of rs1801282 in PPARγ on WC as a continuous outcome. Findings suggest that genetic risk scores based on counting SNPs with relatively high effect sizes, defined based on populations with European ancestry, can sufficiently allow estimation of genetic susceptibility for Roma. Further studies are needed to clarify the role of SNP(s) with protective effect(s).
机译:对遗传因素对肥胖发展的影响的调查在罗马人口 - 欧洲欧洲的最大和最脆弱的少数群体有限。从遗传结合研究中鉴定的遗传变异主要来自欧洲群体。考虑到这一点,我们调查选定肥胖相关的单核苷酸多态性(SNP),从欧洲血统的匈牙利一般(HG)群体中获得,在匈牙利罗姆人(HR)人口数据的适用性。易受影响等位基因中的20个预选的SNP,已知与肥胖相关的表型显着相关,用于估计Hg(n = 1783)和HR中的这些SNP对体重指数(BMI)和腰围(WC)的影响( n = 1225)人群。使用线性和逻辑回归模型测试单个SNP关联,调整已知的协变量。在20个SNP中,四个位于FTO(RS1121980,RS1558902,RS9939609和RS9941349)中显示出与BMI和WC的强烈关联,作为两个样品中的连续变量。基于成人治疗委员会III(ATPIII)和国际糖尿病联合会(IDF)欧洲和亚洲标准的计算在FTO中展示了仅在群体中与WC相关联的FTS941349,以及仅与WC相关的TMEM18中的两个SNP(RS2867125,RS6548238)。在人口中。仅在WC的PPARγ中的Rs1801282的情况下仅观察到具有显着差异(方向和效果大小)作为连续结果。研究结果表明,基于计数SNP的遗传风险评分,基于欧洲血统的群体定义,可以充分允许估算罗马的遗传易感性。需要进一步的研究来阐明SNP的作用与保护作用。

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