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中国汉族人血管紧张素转换酶基因多态性与糖尿病视网膜病变相关性Meta分析
Meta-analysis of the association between the insertion/deletion polymorphism of the angiotensin converting enzyme gene and diabetic retinopathy
【摘要】 目的对中国汉族人血管紧张素转换酶基因(ACE)内含子16插入(Ⅰ)/缺失(D)多态性与糖尿病视网膜病变(DR)的关联性进行Meta分析。方法以糖尿病视网膜病变组和糖尿病对照组基因型分布的比值比(OR)为统计量,应用REVMAN4.2软件对各研究结果进行一致性检验和数据合并。结果相关文献未发现显著发表偏倚。研究共包括糖尿病视网膜病变组729例,糖尿病对照组903例,数据合并结果DD/(ID+Ⅱ)OR值为1.80,95%可信区间(CI)为1.29~2.50。Ⅱ/(ID+DD)OR值为0.67,95%CI为0.54~0.84。结论汉族人群ACEI/D多态性与DR有关联,糖尿病视网膜病变组DD基因型增多,Ⅱ基因型减少。
【Abstract】 Objective To study the association between the insertion(Ⅰ)/deletion(D) polymorphism of the angiotensin converting enzyme geneintron 16 (ACE/ID) and diabetic retinopathy (DR) in Chinese population by the means of meta-analysis. Methods Odds ratios of ACE/ID genotype distributions in DR patients against diabetic patients without retinopathy were analysed . The meta-analysis software, REVMAN 4.2,was applied for investigating hetero geneity among individual studies and summarizing effects across studies. Results A total of 729 cases and 903 controls from 13 studies were in cluded. No significant publication bias has been found. The pooled odds ratio (with 95% CI) of DDvs ID + Ⅱ was 1.80 (1.29~2.50),while the pooled odds ration of Ⅱ vs ID+DD was 0.67 (0.54~0.84). Conclusion In Chinese population, ACE I/D polymorphism is associated with DR. The number of DR patients with DD genotype increases while that with Ⅱ genotype decreases.
【Key words】 polymorphism(genetics); gene; diabetic retinopathy /genetics; peptidyl-dipeptidase A/genetics; meta-(analysis);
- 【文献出处】 安徽医科大学学报 ,Acta Universitis Medicinalis Nahui , 编辑部邮箱 ,2005年03期
- 【分类号】R587.2
- 【被引频次】8
- 【下载频次】223