1Department of Ophthalmology and Visual Sciences, Kyoto University Graduate School of Medicine, Kyoto, Japan.
2Center for Genomic Medicine, Kyoto University Graduate School of Medicine, Kyoto, Japan.
Commun Biol. 2019 Dec 12;2:468. doi: 10.1038/s42003-019-0712-z. eCollection 2019.
The recently emerged pachychoroid concept has changed the understanding of age-related macular degeneration (AMD), which is a major cause of blindness; recent studies attributed AMD in part to pachychoroid disease central serous chorioretinopathy (CSC), suggesting the importance of elucidating the CSC pathogenesis. Our large genome-wide association study followed by validation studies in three independent Japanese and European cohorts, consisting of 1546 CSC samples and 13,029 controls, identified two novel CSC susceptibility loci: and near (rs13278062, odds ratio = 1.35, = 1.26 × 10; rs6061548, odds ratio = 1.63, = 5.36 × 10). A T allele at rs13278062, a risk allele for CSC, is known to be a risk allele for AMD. This study not only identified new susceptibility genes for CSC, but also improves the understanding of the pathogenesis of AMD.
最近出现的脉络膜增厚概念改变了人们对年龄相关性黄斑变性(AMD)的认识,AMD 是导致失明的主要原因之一;最近的研究部分归因于脉络膜增厚疾病中心性浆液性脉络膜视网膜病变(CSC),这表明阐明 CSC 发病机制的重要性。我们的全基因组关联研究随后在三个独立的日本和欧洲队列中进行了验证研究,包括 1546 个 CSC 样本和 13029 个对照,确定了两个新的 CSC 易感性位点: 和附近 (rs13278062,优势比=1.35, = 1.26 × 10;rs6061548,优势比=1.63, = 5.36 × 10)。在 rs13278062 处的 T 等位基因是 CSC 的风险等位基因,已知是 AMD 的风险等位基因。这项研究不仅确定了 CSC 的新易感基因,而且还提高了对 AMD 发病机制的理解。