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Association of adiponectin gene polymorphisms and additional gene-gene interaction with nonalcoholic fatty liver disease in the Chinese Han population

机译:脂联素基因多态性与其他基因-基因相互作用与中国汉族人群非酒精性脂肪肝的关联

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PurposeTo investigate the association between the single nucleotide polymorphisms (SNPs) of the adiponectin gene and nonalcoholic fatty liver disease (NAFLD) as well as the impact of the interaction of multiple SNPs on NAFLD risk, based on a Chinese population study.MethodsA total of 612 subjects (411 male, 201 female) were selected, including 302 NAFLD patients and 310 controls. Three SNPs were selected for genotyping in the case-control study: rs266729, rs822393, and rs1501299. A logistic regression model was used to examine the interaction between the SNPs and NAFLD. The odds ratio (OR) and 95?% confidence interval (95?% CI) were calculated. Generalized multifactor dimensionality reduction (GMDR) was employed to analyze the interaction among SNPs.ResultsLogistic analysis showed a significant association between genotypes of variants in rs266729 and rs822393 and increased NAFLD risk. The carriers of the homozygous mutant of two SNP polymorphisms revealed increased NAFLD risk compared to those with wild-type homozygotes; ORs (95?% CI) were 1.31 (1.14–1.81) (p?=?0.001) and 1.18 (1.05–1.71) (p?=?0.005), respectively. There was a significant two-locus model (p?=?0.0010) involving rs266729 and rs822393, indicating a potential gene-gene interaction between rs266729 and rs822393. Overall, the two-locus models had a cross-validation consistency of 10 and testing accuracy of 62.17?%. Subjects with the CG or GG and CT or TT genotype have the highest NAFLD risk compared to subjects with the CC-CC genotype; the OR (95?% CI) was 2.52 (1.31–3.82), p?
机译:目的根据一项中国人群研究,研究脂联素基因的单核苷酸多态性(SNP)与非酒精性脂肪肝疾病(NAFLD)的关联以及多种SNP相互作用对NAFLD风险的影响。选择受试者(男411名,女201名),包括302名NAFLD患者和310名对照。在病例对照研究中,选择了三个SNP进行基因分型:rs266729,rs822393和rs1501299。使用逻辑回归模型检查SNP与NAFLD之间的相互作用。计算比值比(OR)和95%置信区间(95%CI)。结果:Logistic分析显示rs266729和rs822393变异的基因型与NAFLD风险增加之间存在显着的关联,并通过广义多因素降维(GMDR)分析了SNP之间的相互作用。与野生型纯合子相比,具有两个SNP多态性的纯合突变体的携带者显示出NAFLD风险增加。 ORs(95%CI)为1.31(1.14–1.81)(p?=?0.001)和1.18(1.05–1.71)(p?=?0.005)。有一个涉及rs266729和rs822393的显着两基因座模型(p?=?0.0010),表明rs266729和rs822393之间存在潜在的基因-基因相互作用。总体而言,两基因座模型的交叉验证一致性为10,测试准确性为62.17%。与具有CC-CC基因型的受试者相比,具有CG或GG和CT或TT基因型的受试者的NAFLD风险最高;协变量调整后,OR(95 %% CI)为2.52(1.31-3.82),p 0.001。结论我们的结果支持rs266729(?11377 G / C)和rs822393(?4522 C / T)的重要关联。 )多态性会增加NAFLD的风险。相互作用分析显示,rs266729和rs822393对NAFLD具有联合作用。

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