Shared genetic variants for polypoidal choroidal vasculopathy and typical neovascular age-related macular degeneration in East Asians.

Journal Article (Journal Article)

Polypoidal choroidal vasculopathy (PCV), a subtype of age-related macular degeneration (AMD) more frequently seen in East Asians, has both common and distinct clinical manifestations with typical neovascular AMD (tAMD). We aim to examine the extent to which common genetic variants are shared between these two subtypes. We performed the meta-analysis of association in a total of 1062 PCV patients, 1157 tAMD patients and 5275 controls of East Asian descent from the Genetics of AMD in Asians Consortium at the 34 known AMD loci. A total of eight loci were significantly associated with PCV, including age-related maculopathy susceptibility 2 (ARMS2)-HtrA serine peptidase 1 (HTRA1), complement factor H (CFH), C2-CFB-SKIV2L, CETP, VEGFA, ADAMTS9-AS2 and TGFBR1 (P<5 × 10-4) from the single-nucleotide polymorphism-based test and COL4A3 from the gene-based tests (Pgene=2.02 × 10-4). PCV and tAMD are genetically highly correlated (rg=0.69, P=4.68 × 10-3), with AMD known loci accounting for up to 36% variation. Weaker association for PCV was observed at ARMS2-HTRA1 (Pdif=4.39 × 10-4) and KMT2E-SRPK2(Pdif=4.43 × 10-3), compared with tAMD. Variants at CFH, CETP and VEGFA exhibited different association signals in East Asians, in contrast to those in European individuals. Our data suggest a substantially shared genetic susceptibility for PCV and tAMD, while also highlight the unique associations for PCV, which is useful in understanding the pathogenesis of PCV.

Full Text

Duke Authors

Cited Authors

  • Fan, Q; Cheung, CMG; Chen, LJ; Yamashiro, K; Ahn, J; Laude, A; Mathur, R; Mun, CC; Yeo, IY; Lim, TH; Teo, Y-Y; Khor, CC; Park, K-H; Yoshimura, N; Pang, CP; Wong, TY; Cheng, C-Y

Published Date

  • December 2017

Published In

Volume / Issue

  • 62 / 12

Start / End Page

  • 1049 - 1055

PubMed ID

  • 28835638

Electronic International Standard Serial Number (EISSN)

  • 1435-232X

Digital Object Identifier (DOI)

  • 10.1038/jhg.2017.83


  • eng

Conference Location

  • England