Luo Shasha, Shi Chao, Wang Furu, Wu Zhifeng
Department of Ophthalmology, Nanjing Medical University Affiliated Wuxi Second Hospital, 68 Zhongshan Road, Wuxi 214002, China.
Wuxi Center for Disease Control and Prevention, 499 Jincheng Road, Wuxi 214023, China.
Int J Environ Res Public Health. 2016 Nov 15;13(11):1142. doi: 10.3390/ijerph13111142.
Aims-to address the inconclusive findings of the association of angiotensin-converting enzyme (ACE) insertion/deletion (I/D) polymorphism on risk of diabetic retinopathy (DR), a meta-analysis was conducted. Methods-we conducted a meta-analysis on 4252 DR cases and 5916 controls from 40 published studies by searching electronic databases and reference lists of relevant articles. A random-effects or fixed-effects model was used to estimate the overall and stratification effect sizes on I/D polymorphism on the risk of DR. Results-we found a significant association between the ACE I/D polymorphism and the risk of DR for all genetic model (ID vs. II: OR = 1.14, 95% CI: 1.00-1.30; DD vs. II: OR = 1.38, 95% CI: 1.11-1.71; Allele contrast: OR = 1.17, 95% CI: 1.05-1.30; recessive model: OR = 1.24, 95% CI: 1.02-1.51 and dominant model: OR = 1.21, 95% CI: 1.06-1.38, respectively). In stratified analysis by ethnicity and DM type, we further found that the Asian group with T2DM showed a significant association for all genetic models (ID vs. II: OR = 1.14, 95% CI: 1.01-1.30; DD vs. II: OR = 1.54, 95% CI: 1.14-2.08; Allele contrast: OR = 1.26, 95% CI: 1.09-1.47; recessive model: OR = 1.42, 95% CI: 1.07-1.88 and dominant model: OR = 1.26, 95% CI: 1.07-1.49, respectively). Conclusion-our study suggested that the ACE I/D polymorphism may contribute to DR development, especially in the Asian group with type 2 diabetes mellitus (T2DM). Prospective and more genome-wide association studies (GWAS) are needed to clarify the real role of the ACE gene in determining susceptibility to DR.
目的——为解决血管紧张素转换酶(ACE)插入/缺失(I/D)多态性与糖尿病视网膜病变(DR)风险之间关联的不确定研究结果,进行了一项荟萃分析。方法——通过检索电子数据库和相关文章的参考文献列表,我们对40项已发表研究中的4252例DR病例和5916例对照进行了荟萃分析。采用随机效应或固定效应模型来估计I/D多态性对DR风险的总体和分层效应大小。结果——我们发现,在所有遗传模型中,ACE I/D多态性与DR风险之间存在显著关联(ID与II相比:OR = 1.14,95%CI:1.00 - 1.30;DD与II相比:OR = 1.38,95%CI:1.11 - 1.71;等位基因对比:OR = 1.17,95%CI:1.05 - 1.30;隐性模型:OR = 1.24,95%CI:1.02 - 1.51;显性模型:OR = 1.21,95%CI:1.06 - 1.38)。在按种族和糖尿病类型进行的分层分析中,我们进一步发现,患有2型糖尿病(T2DM)的亚洲人群在所有遗传模型中均显示出显著关联(ID与II相比:OR = 1.14,95%CI:1.01 - 1.30;DD与II相比:OR = 1.54,95%CI:1.14 - 2.08;等位基因对比:OR = 1.26,95%CI:1.09 - 1.47;隐性模型:OR = 1.42,95%CI:1.07 - 1.88;显性模型:OR = 1.26,95%CI:1.07 - 1.49)。结论——我们的研究表明,ACE I/D多态性可能促进DR的发展,尤其是在患有2型糖尿病(T2DM)的亚洲人群中。需要进行前瞻性和更多全基因组关联研究(GWAS)来阐明ACE基因在确定DR易感性方面的真正作用。