标题：GWAS study using DNA pooling strategy identifies association of variant rs4910623 in OR52B4 gene with anti-VEGF treatment response in age-related macular degeneration
摘要：Pooled DNA based GWAS to determine genetic association of SNPs with visual acuity (VA) outcome in anti-vascular endothelial growth factor (anti-VEGF) treated neovascular age-related macular degeneration (nAMD) patients. We performed pooled DNA based GWAS on 285 anti-VEGF treated nAMD patients using high density Illumina 4.3 M array. Primary outcome was change in VA in Early Treatment Diabetic Retinopathy Study (ETDRS) letters after 6 months of anti-VEGF treatment (patients who lost ≥5 ETDRS letters classified as non-responders and all remaining classified as responders). GWAS analysis identified 44 SNPs of interest: 37 with strong evidence of association (p < 9 × 10(-8)), 2 in drug resistance genes (p < 5 × 10(-6)) and 5 nonsynonymous changes (p < 1 × 10(-4)). In the validation phase, individual genotyping of 44 variants showed three SNPs (rs4910623 p = 5.6 × 10(-5), rs323085 p = 6.5 × 10(-4) and rs10198937 p = 1.30 × 10(-3)) remained associated with VA response at 6 months. SNP rs4910623 also associated with treatment response at 3 months (p = 1.5 × 10(-3)). Replication of these three SNPs in 376 patients revealed association of rs4910623 with poor VA response after 3 and 6 months of treatment (p = 2.4 × 10(-3) and p = 3.5 × 10(-2), respectively). Meta-analysis of both cohorts (673 samples) confirmed association of rs4910623 with poor VA response after 3 months (p = 1.2 × 10(-5)) and 6 months (p = 9.3 × 10(-6)) of treatment in nAMD patients.
