[No authors listed]
OBJECTIVE:To investigate the potential correlation between complement factor B polymorphisms and age-related macular degeneration. METHODS:We retrieved relevant articles systematically by searching PubMed and Web of Science databases. The pooled odds ratios and 95% confidence intervals were calculated for five complement factor B polymorphism rs641153, rs4151667, rs1048709, rs2072633, and rs12614 using data from included articles in both random effects and fixed effect models. Subgroup meta-analysis based on age-related macular degeneration type, choroidal neovascular disease (rs641153 and rs4151667), geographic atrophy (rs641153 and rs4151667), and races was also performed. RESULTS:In the overall comparison, we observed that the distribution of rs641153 and the risk of age-related macular degeneration were significantly correlated (pâ<â0.00001). Similar results were obtained in subgroup analysis based on race (Caucasians, pâ<â0.00001; Asians, pâ=â0.003) and age-related macular degeneration type (choroidal neovascular disease, pâ<â0.00001; geographic atrophy, pâ=â0.04). As for complement factor B rs4151667, the genotypic effects were also demonstrated statistically significant in overall analysis (pâ<â0.00001) and only in Caucasians diagnosed with choroidal neovascular disease (pâ=â0.004), but not in Asians. Moreover, no statistically significant correlations between the complement factor B polymorphisms rs1048709 (pâ=â0.63), rs2072633 (pâ=â0.72), rs12614 (pâ=â0.98) and susceptibility to age-related macular degeneration were detected in either overall or subgroup analysis. CONCLUSION:Collectively, we demonstrated that the complement factor B genes rs641153 and rs4151667, but not rs1048709, rs2072633, rs12614, were associated with the susceptibility of age-related macular degeneration and might play predictive roles in future age-related macular degeneration diagnosis. More studies are needed to verify these findings.
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