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类风湿关节炎的遗传学。

The genetics of rheumatoid arthritis.

机构信息

UCL Medical School, London, UK.

出版信息

Rheumatology (Oxford). 2020 Oct 1;59(10):2661-2670. doi: 10.1093/rheumatology/keaa232.

Abstract

RA is a chronic systemic inflammatory disease that primarily affects the small joints of the hands and feet, and results in a mean reduction in life expectancy of 3-10 years. RA is a multigene disorder with a substantial genetic component and a heritability estimate of 60%. Large-scale Genome-Wide Association Studies (GWAS) and meta-analyses have revealed common disease-associated variants in the population that may contribute cumulatively to RA pathogenesis. This review identifies the most significant genetic variants associated with RA susceptibility to date, with particular focus on the contribution of the HLA class II genes across different ethnic groups. Also discussed are the potential applications of pharmacogenomics to RA management by identifying polymorphisms associated with variation in treatment response or toxicity. The use of genetic variants to guide treatment strategy has the potential to not only reduce National Health Service costs, but also drastically improve patient experience and quality of life.

摘要

类风湿关节炎是一种慢性全身性炎症性疾病,主要影响手和脚的小关节,导致预期寿命平均缩短 3-10 年。类风湿关节炎是一种多基因疾病,具有重要的遗传成分,遗传度估计为 60%。大规模全基因组关联研究(GWAS)和荟萃分析揭示了人群中常见的与疾病相关的变异,这些变异可能共同促成类风湿关节炎的发病机制。本综述确定了迄今为止与类风湿关节炎易感性相关的最重要的遗传变异,特别关注 HLA 类 II 基因在不同种族群体中的贡献。还讨论了通过鉴定与治疗反应或毒性变化相关的多态性,将药物基因组学应用于类风湿关节炎管理的潜在应用。利用遗传变异来指导治疗策略不仅有可能降低国民保健服务的成本,还可以极大地改善患者的体验和生活质量。

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