摘要
目的:探讨PLIN基因rs2304796及rs894160位点多态性与河南汉族人群2型糖尿病的关系。方法:采用随机整群抽样的方法收集河南省农村地区2型糖尿病患者161人和非糖尿病患者1113人,应用PCR-RFLP和荧光定量PCR技术检测PLIN基因rs2304796和rs894160位点的多态性。用Unphased 3.0.7软件构建单倍型,用logistic回归模型分析该基因变异对2型糖尿病发生的影响。结果:2型糖尿病患者和非患者中PLIN基因rs2304796位点基因型频率和等位基因频率分布差异有统计学意义(χ2=6.018,P=0.049;χ2=5.916,P=0.015),rs894160位点基因型频率和等位基因频率分布差异无统计学意义(χ2=0.680和0.295,P>0.05)。 Logistic回归分析结果显示,在调整了人口统计学特征、肥胖及血脂测量指标后,rs2304796位点CT或TT基因型携带者患2型糖尿病的危险性降低[ OR(95%CI)=0.670(0.475~0.944)]。结论:PLIN基因rs2304796位点CT或TT基因型可能是2型糖尿病的保护性因素。
Aim:To investigate the polymorphism of rs2304796 and rs894160 loci of PLIN gene in patients with type 2 diabetes from Henan Han population .Methods:A total of 1 274 adults (161 type 2 diabeties and 1 113 controls) were re-cruited.PLIN rs2304796 polymorphism was genotyped by PCR-RFLP and PLIN rs894160 was genotyped by Real-time PCR. The software Unphased 3.0.7 was performed to construct the haplotypes of every individual .Association between PLIN poly-morphism and type 2 diabetes was estimated by logistic regression model adjusted for covariates .Results:Genotype and al-lele frequency of rs2304796 between the 2 populations had statistical difference (χ2 =6.018,P=0.049, χ2 =5.916,P=0.015).There were no statistical differences in rs894160 genotype and allele frequency between type 2 diabeties and controls (χ2 =0.680,0.295,P〉0.05).Data from logistic analysis revealed that (CT+TT)of PLIN gene rs2304796 polymorphism de-creased the risk of type 2 diabetes after adjusting obesity and blood liqid indexes [OR(95%CI)=0.670(0.475-0.944)]. Conclusion:The SNP(CT+TT)in rs2304796 of PLIN gene might be a protective factor for type 2 diabetes.
出处
《郑州大学学报(医学版)》
CAS
北大核心
2013年第5期633-636,共4页
Journal of Zhengzhou University(Medical Sciences)
基金
国家自然科学基金资助项目30671805
河南省医学科技攻关计划基金资助项目2011020084