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作 者:钱莉[1] 徐宽枫[1] 刘璇[1] 单珊[1] 杨涛[1]
机构地区:[1]南京医科大学第一附属医院内分泌科,210029
出 处:《中华糖尿病杂志》2011年第5期376-379,共4页CHINESE JOURNAL OF DIABETES MELLITUS
摘 要:目的评价SLC30A8基因rs13266634位点C/T多态性与1型糖尿病的关系。方法选取2008年9月至2010年11月就诊于江苏省人民医院及其25家合作单位的351例1型糖尿病患者(糖尿病组),其中男183例,女168例,平均年龄(20±11)岁。同期于江苏省人民医院体检中心选取429名健康志愿者(健康对照组),其中男201例,女228例,平均年龄(23±4)岁。所有研究对象均行SLC30A8基因rs13266634位点C/T多态性分析。检索Pubmed及中文期刊CNKI数据库,入选有关SLC30A8基因rs13266634位点多态性与1型糖尿病的病例对照研究,进行meta分析。结果病例对照研究表明,糖尿病组与健康对照组SLC30A8rs13266634基因分布频率无显著差异[比值比(OR)为0.96,95%可信区间(95% CI)=0.79~1.18,P=0.71]。共有5篇文献纳入nleta分析,其中1型糖尿病患者10646例,健康对照者10242名。2组异质性检验,2为0%,异质性检验P值为0.595,无显著异质性,故采用固定效应模型进行数据合并。纳入研究的合并OR值为1.02,95%C/为0.98~1.06,P值为0.38。Begg’s检验中P值为0.155,即纳入研究无发表偏倚。结论病例对照研究及meta分析结果均表明SLC30A8基因rs13266634位点C/T多态性与1型糖尿病易患性无显著关联。Objective To evaluate the relationship between SLC30A8 gene rs13266634 C/T polymorphism and type 1 diabetes mellitus (T1DM). Methods A total of 351 T1 DM patients and 429 healthy subjects were enrolled in this case-control study from September 2008 to November 2010. The TI DM group included 183 males and 168 females, aged (20 ± 11 ) years; and the control group included 201 males and 228 females, aged ( 23 ± 4 ) years. All the participants underwent genotyping of the SLC30A8 gene rs13266634 polymorphism. In addition, systematic review and recta-analysis of the publishing literature on genetic association of SLC30A8 rs13266634 polymorphism and T1DM were performed in Pubmed and CNKI. Results Our case-control study showed that rs13266634 C/T polymorphism was not associated with TI DM (odds ratio =0. 96, 95% confidence interval (95% CI) =0. 79 to 1.18, P =0. 71 ). The literature search identified 5 studies that analyzed the association of the SLC30A8 gene rs13266634 polymorphism with T1DM, including 10 646 TIDM patients and 10 207 healthy controls. Since I^2 = 0% and Pheterogeneity = 0. 595, all the studies were combined with fixed effects model. Odds ratios of C allele to T allele was 1.02 (95% CI: 0. 98 to 1.06, P =0. 38) , and Begg' s test revealed no significant publication bias. Conclusion Our results indicate that SLC30A8 gene rs13266634 polymorphism is not associated with increased risk of TI DM.
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