Association of PEDF polymorphisms with age-related macular degeneration and polypoidal choroidal vasculopathy: a systematic review and meta-analysis

• Published in: Scientific reports 2015-03, Vol.5 (1), p.9497-9497, Article 9497
• Main Authors: Ma, Li, Tang, Shu Min, Rong, Shi Song, Chen, Haoyu, Young, Alvin L., Kumaramanickavel, Govindasamy, Pang, Chi Pui, Chen, Li Jia
• Format: Article
• Language: English
• Subjects: 692/499; 692/699/3161/1626; Age; Alleles; Epithelium; Eye Proteins - genetics; Genetic Association Studies; Genetic Predisposition to Disease; Genotype; Genotyping; Humanities and Social Sciences; Humans; Macular degeneration; Macular Degeneration - genetics; Meta-analysis; Minority & ethnic groups; multidisciplinary; Nerve Growth Factors - genetics; Odds Ratio; Pigment epithelium-derived factor; Polymorphism, Single Nucleotide; Science; Serpins - genetics; Studies; Vascular diseases
• ISSN: 2045-2322; 2045-2322
• DOI: 10.1038/srep09497

This study assesses the association of the pigment epithelium-derived factor (PEDF) gene with age-related macular degeneration (AMD) and polypoidal choroidal vasculopathy (PCV). Publications in MEDLINE and EMBASE up to 21/08/2014 were searched for case-control association studies of PEDF with AMD and/or PCV. Reported studies giving adequate genotype and/or allele information were included. Pooled odds ratios (OR) and 95% confidence intervals (CI) of each polymorphism were estimated. Our literature search yielded 297 records. After excluding duplicates and reports with incomplete information, 8 studies were eligible for meta-analysis, involving 2284 AMD patients versus 3416 controls and 317 PCV patients versus 371 controls. Four PEDF polymorphisms were meta-analyzed: rs1136287, rs12150053, rs12948385 and rs9913583, but none was significantly associated with AMD or PCV. The most-investigated polymorphism, rs1136287, had a pooled-OR of 1.02 (95% CI: 0.94–1.11, P = 0.64) for AMD. In subgroup analysis by ethnicity, no significant association was identified. Polymorphisms present in single report showed no association. Therefore, existing data in literature does not support the role of PEDF in the genetic susceptibility of AMD and PCV, although replication in specific populations is warranted. Since the pooled-sample size for PCV was small, there is a need of PEDF genotyping in larger samples of PCV.