首页> 美国卫生研究院文献>other >No Interaction with Alcohol Consumption but Independent Effect of C12orf51 (HECTD4) on Type 2 Diabetes Mellitus in Korean Adults Aged 40-69 Years: The KoGES_Ansan and Ansung Study
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No Interaction with Alcohol Consumption but Independent Effect of C12orf51 (HECTD4) on Type 2 Diabetes Mellitus in Korean Adults Aged 40-69 Years: The KoGES_Ansan and Ansung Study

机译:KoGES_Ansan和Ansung研究表明与酒精消耗没有相互作用但C12orf51(HECTD4)对40-69岁韩国成年人2型糖尿病的独立影响

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摘要

Previously, genetic polymorphisms of C12orf51 (HECTD4) (rs2074356 and/or rs11066280) have been shown to be related to alcohol consumption and type 2 diabetes (T2D). This study aimed to prospectively examine whether C12orf51 had an interaction with or independent effect on alcohol consumption and the risk of T2D. The present study included 3,244 men and 3,629 women aged 40 to 69 years who participated in the Korean Genome and Epidemiology Study (KoGES)_Ansan and Ansung Study. Cox proportional hazards models were used to estimate HRs and 95% CIs for T2D. rs2074356 and rs11066280 were associated with the risk of T2D after adjusting for alcohol consumption (rs2074356 for AA: HR = 0.39 and 95% CI = 0.17–0.87 in men, and HR = 0.36 and 95% CI = 0.13–0.96 in women; rs11066280 for AA: HR = 0.44 and 95% CI = 0.23–0.86 in men, and HR = 0.39 and 95% CI = 0.16–0.94 in women). We identified that the association of each variant (rs2074356 and rs11065756) in C12orf51 was nearly unchanged after adjusted for alcohol consumption. Therefore, the association of 2 SNPs in C12orf51 with diabetes may not be mediated by alcohol use. There was no interaction effect between alcohol consumption and the SNPs with T2D. However, even in never-drinkers, minor allele homozygote strongly influenced T2D risk reduction (rs2074356 for AA: HR = 0.35, 95% CI = 0.14–0.90, and p-trend = 0.0035 in men and HR = 0.34, 95% CI = 0.13–0.93, and p-trend = 0.2348 in women; rs11066280 for AA: HR = 0.36, 95% CI = 0.16–0.82, and p-trend = 0.0014 in men and HR = 0.39, 95% CI = 0.16–0.95, and p-trend = 0.3790 in women), while alcohol consumption did not influence the risk of T2D within each genotype. rs2074356 and rs11066280 in or near C12orf51, which is related to alcohol drinking behavior, may longitudinally decrease the risk of T2D, but not through regulation of alcohol consumption.
机译:以前,C12orf51(HECTD4)(rs2074356和/或rs11066280)的遗传多态性已显示与饮酒和2型糖尿病(T2D)相关。这项研究旨在前瞻性地检查C12orf51是否与酒精消耗和T2D风险有相互作用或独立影响。本研究包括年龄在40至69岁之间的3244名男性和3629名女性,他们参加了韩国基因组和流行病学研究(KoGES)_安山和安盛研究。使用Cox比例风险模型来估算T2D的HR和95%CI。调整酒精摄入后,rs2074356和rs11066280与T2D风险相关(AA的rs2074356:男性HR = 0.39和95%CI = 0.17-0.87,女性HR = 0.36和95%CI = 0.13-0.96; rs11066280对于AA:男性HR = 0.44和95%CI = 0.23–0.86,女性HR = 0.39和95%CI = 0.16-0.94)。我们确定,在调整了酒精消耗后,C12orf51中每个变体(rs2074356和rs11065756)的关联几乎不变。因此,C12orf51中2个SNP与糖尿病的关联可能不会通过饮酒来介导。饮酒与使用T2D的SNP之间没有相互作用。然而,即使在从不饮酒的情况下,较小的等位基因纯合子也强烈影响T2D风险的降低(AA的rs2074356:男性HR = 0.35,95%CI = 0.14-0.90,p趋势= 0.0035,HR = 0.34,95%CI =女性为0.13–0.93,p趋势= 0.2348; AA的rs11066280:男性HR = 0.36,95%CI = 0.16-0.82,男性p-趋势= 0.0014,HR = 0.39,95%CI = 0.16-0.95,而女性的p趋势= 0.3790),而饮酒并没有影响每种基因型中T2D的风险。与饮酒行为有关的C12orf51中或附近的rs2074356和rs11066280可以纵向降低T2D的风险,但不能通过调节饮酒量来实现。

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