Wang Qin, Zhao Hai-Sheng, Li Li
Department of Ophthalmology, the Second Affiliated Hospital of Chongqing Medical University, Chongqing 400010, China; Center of Ophthalmology, the Second Affiliated Hospital of Chongqing Medical University, Chongqing 400010, China.
Department of Ophthalmology, the Second Affiliated Hospital of Chongqing Medical University, Chongqing 400010, China.
Int J Ophthalmol. 2016 Feb 18;9(2):298-305. doi: 10.18240/ijo.2016.02.23. eCollection 2016.
To systematically review the association between complement factors I (CFI) polymorphisms and age-related macular degeneration (AMD) and to explore whether CFI polymorphisms are associated with AMD.
Meta-analysis of articles published from 1995 to January 2015 of articles involved with AMD and polymorphisms of the CFI gene. Eligible data were pooled in a Meta-analysis, analyzing using STATA software (version 12.0), Review Manager (version 5.2) and different models based on the heterogeneity of effect sizes. Egger's test, Begg's rank correlation methods were used to evaluate for publication bias.
Thirteen articles were eligible, describing two loci polymorphisms of the CFI gene (of which 12 articles focus on rs10033900T>C and 3 articles focus on rs2285714C>T). For rs10033900T>C, the results of our study revealed that having a mutant allele C, TC, CC and TC+CC was associated with a decreased risk of AMD in all population groups studied (C versus T models, OR=0.84, 95%CI: 0.72-0.99, P=0.04; TC versus TT models OR=0.89, 95%CI: 0.88-0.99, P=0.04; CC versus TT models, OR=0.76, 95%CI: 0.60-0.98, P=0.03; TC+CC versus TT models, OR=0.81, 95%CI:0.65-0.99, P=0.04). We found that C allele were related to lower AMD risk in the Caucasian population by subgroup analysis, but there was no association with AMD under the allele and genotypes comparison in Asian studies. For rs2285714 C>T, the TC, TT genotypes contributed to a higher risk of AMD, compared with the CC carriers and TC+CC (OR=1.34, 95%CI: 1.09-1.63, P=0.004; OR=1.50, 95%CI: 1.25-1.80, P<0.0001).
This Meta-analysis suggests that CFI rs10033900T>C and rs2285714C>T polymorphisms may contribute to AMD.
系统评价补体因子I(CFI)基因多态性与年龄相关性黄斑变性(AMD)之间的关联,并探讨CFI基因多态性是否与AMD相关。
对1995年至2015年1月发表的有关AMD与CFI基因多态性的文章进行荟萃分析。符合条件的数据汇总进行荟萃分析,使用STATA软件(12.0版)、Review Manager(5.2版)并根据效应大小的异质性采用不同模型进行分析。采用Egger检验、Begg秩相关法评估发表偏倚。
13篇文章符合条件,描述了CFI基因的两个位点多态性(其中12篇文章关注rs10033900T>C,3篇文章关注rs2285714C>T)。对于rs10033900T>C,我们的研究结果显示,在所有研究的人群组中,携带突变等位基因C、TC、CC以及TC+CC与AMD风险降低相关(C与T模型比较,OR=0.84,95%CI:0.72-0.99,P=0.04;TC与TT模型比较,OR=0.89,95%CI:0.88-0.99,P=0.04;CC与TT模型比较,OR=0.76,95%CI:0.60-0.98,P=0.03;TC+CC与TT模型比较,OR=0.81,95%CI:0.65-0.99,P=0.04)。通过亚组分析我们发现,在白种人群中C等位基因与较低的AMD风险相关,但在亚洲研究的等位基因和基因型比较中未发现与AMD有关联。对于rs2285714C>T,与CC携带者以及TC+CC相比,TC、TT基因型导致更高的AMD风险(OR=1.34,95%CI:1.09-1.63,P=0.004;OR=I.50,95%CI:1.25-1.80,P<0.0001)。
这项荟萃分析表明,CFI基因的rs10033900T>C和rs2285714C>T多态性可能与AMD有关。