Identifying common genetic etiologies between iridocyclitis and related immune-mediated diseases

确定虹膜睫状体炎与相关免疫介导疾病的共同遗传病因

阅读:2

Abstract

BACKGROUND: Patients with iridocyclitis are at heightened risk for immune-mediated diseases. The genetic underpinnings of iridocyclitis are intricate, necessitating an integrated approach to unravel the genetic connections between iridocyclitis and these diseases. METHODS: GWAS data were integrated from three databases using METAL. Independent risk loci were analyzed through conditional and joint genome-wide multi-trait analysis, multi-marker genomic annotation, and functional mapping of significant loci. This approach combined quantitative trait loci data and various methodologies to identify genes and proteins associated with risk. Target gene verification was conducted through cell experiments and flow cytometry. RESULTS: The study identified five independent iridocyclitis-related risk loci and 123 associated genes. Additionally, 14 multi-disease risk genes and 109 disease-related proteins were discovered. Flow cytometry confirms that FBXL18 and IL15RA are responsive to inflammatory stimuli and supports their role in immune-mediated pathways relevant to iridocyclitis, underscoring its potential as a therapeutic target. CONCLUSION: This study indicates that the polygenic factors shared between iridocyclitis and immune-mediated diseases are broadly distributed across the genome. These findings affirm a genetic link between iridocyclitis and immune-mediated diseases and highlight new therapeutic targets for these conditions.

特别声明

1、本页面内容包含部分的内容是基于公开信息的合理引用;引用内容仅为补充信息,不代表本站立场。

2、若认为本页面引用内容涉及侵权,请及时与本站联系,我们将第一时间处理。

3、其他媒体/个人如需使用本页面原创内容,需注明“来源:[生知库]”并获得授权;使用引用内容的,需自行联系原作者获得许可。

4、投稿及合作请联系:info@biocloudy.com。