Genome-Wide Association Study of Age-Related Macular Degeneration Reveals 2 New Loci Implying Shared Genetic Components with Central Serous Chorioretinopathy

Masato Akiyama, Masahiro Miyake, Yukihide Momozawa, Satoshi Arakawa, Maiko Maruyama-Inoue, Mikiko Endo, Yusuke Iwasaki, Kazuyoshi Ishigaki, Nana Matoba, Yukinori Okada, Miho Yasuda, Yuji Oshima, Shigeo Yoshida, Shin ya Nakao, Kazuya Morino, Yuki Mori, Ai Kido, Aki Kato, Tsutomu Yasukawa, Ryo ObataYoshimi Nagai, Kanji Takahashi, Kimihiko Fujisawa, Akiko Miki, Makoto Nakamura, Shigeru Honda, Hiroaki Ushida, Tetsuhiro Yasuma, Koji M. Nishiguchi, Ryusaburo Mori, Koji Tanaka, Yu Wakatsuki, Kenji Yamashiro, Kazuaki Kadonosono, Chikashi Terao, Tatsuro Ishibashi, Akitaka Tsujikawa, Koh Hei Sonoda, Michiaki Kubo, Yoichiro Kamatani

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3 Citations (Scopus)

Abstract

Purpose: To investigate the genetic architecture of age-related macular degeneration (AMD) in a Japanese population. Design: Genome-wide association study (GWAS). Participants: Three thousand seven hundred seventy-two patients with AMD and 16 770 control participants from the Japanese population were enrolled in the association analyses. Methods: We conducted a meta-analysis of 2 independent GWASs that included a total of 2663 patients with AMD and 9471 control participants using the imputation reference panel for genotype imputation specified for the Japanese population (n = 3541). A replication study was performed using an independent set of 1109 patients with AMD and 7299 control participants. Main Outcome Measures: Associations of genetic variants with AMD. Results: A meta-analysis of the 2 GWASs identified 6 loci significantly associated with AMD (P < 5.0 × 10–8). Of these loci, 4 were known to be associated with AMD (CFH, C2/FB, TNFRSF10A, and ARMS2), and 2 were novel (rs4147157 near WBP1L and rs76228488 near GATA5). The newly identified associations were confirmed in a replication study (P < 0.01). After the meta-analysis of all datasets, we observed strong associations in these loci (P = 1.88 × 10–12 and P = 1.35 × 10–9 for meta-analysis for rs4147157 and rs76228488, respectively). When we looked up the associations in the reported central serous chorioretinopathy (CSC) GWAS conducted in the Japanese population, both loci were associated significantly with CSC (P = 4.86 × 10–3 and P = 4.28 × 10–3 for rs4147157 and rs76228488, respectively). We performed a genetic colocalization analysis for these loci and estimated that the posterior probabilities of shared causal variants between AMD and CSC were 0.39 and 0.60 for WBP1L and GATA5, respectively. Genetic correlation analysis focusing on the epidemiologically suggested clinical risk factors implicated shared polygenic architecture between AMD and smoking cessation (rg [the measure of genetic correlation] = –0.33; P = 0.01; false discovery rate, 0.099). Conclusions: Our findings imply shared genetic components conferring the risk of both AMD and CSC. Financial Disclosure(s): Proprietary or commercial disclosure may be found after the references.

Original languageEnglish
Pages (from-to)361-372
Number of pages12
JournalOphthalmology
Volume130
Issue number4
DOIs
Publication statusPublished - Apr 2023

All Science Journal Classification (ASJC) codes

  • Ophthalmology

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