Genome-wide association and multi-omics analyses provide insights into the disease mechanisms of central serous chorioretinopathy.
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ABSTRACT: Central serous chorioretinopathy (CSC) is a major cause of vision loss, especially in middle-aged men, and its chronic subtype can lead to legal blindness. Despite its clinical importance, the underlying mechanisms of CSC need further clarification. In this study, we conducted a meta-analysis of three genome-wide association studies (GWASs) for CSC consisting of 8811 Asians and Caucasians, followed by replication in an additional 4338 Asians. We identified four genome-wide hits, including a novel hit (rs12960630 at LINC01924-CDH7, Pmeta = 2.97 × 10-9). A phenome-wide association study for rs12960630 showed a positive correlation between its CSC risk allele with plasma cortisol concentration. Expression/splicing quantitative trait loci (QTL) analyses showed an associat
SUBMITTER: Mori Y
PROVIDER: S-EPMC11914043 | biostudies-literature | 2025 Mar
REPOSITORIES: biostudies-literature
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