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遗传因素对类风湿关节炎放射学严重程度的调节作用。

Genetic influences modulating the radiological severity of rheumatoid arthritis.

机构信息

Rheumatology Unit, Medical School, University of Sheffield, Royal Hallamshire Hospital, Sheffield S10 2JF, UK.

出版信息

Ann Rheum Dis. 2010 Mar;69(3):476-82. doi: 10.1136/ard.2009.117721. Epub 2010 Feb 2.

Abstract

This review focuses on the contribution of genetic markers to the severity of radiological damage in rheumatoid arthritis (RA). Currently available biomarkers of more severe disease include elevated erythrocyte sedimentation rates or C-reactive protein levels and rheumatoid factor (RF) or anticyclic citrullinated protein antibodies positivity; however, these biomarkers explain a relatively modest proportion of the variance in radiological damage. An important role of genetic factors on RA severity has recently emerged but studies to date have generally been of low statistical power and many have not been replicated. Genetic markers have a number of advantages over conventional biomarkers; genotypes are stable, measurable at disease onset, remain unchanged by treatment and are amenable to high-throughput assays. The recent advances in genome-wide genetic analysis should lead to a more comprehensive understanding of RA severity genes. This knowledge could be used, along with existing biomarkers, to therapeutically target subjects at risk of poor radiological outcome.

摘要

这篇综述重点探讨了遗传标记物对类风湿关节炎(RA)放射学损伤严重程度的影响。目前,更严重疾病的生物标志物包括红细胞沉降率或 C 反应蛋白水平升高,以及类风湿因子(RF)或抗环瓜氨酸肽抗体阳性;然而,这些生物标志物仅能解释放射学损伤中相对较小的变异比例。遗传因素对 RA 严重程度的重要作用最近已经显现,但迄今为止的研究通常统计效能较低,且许多研究结果未得到重复验证。遗传标记物相对于传统生物标志物具有许多优势;基因型稳定,可在疾病发病时测量,不受治疗影响,并且适用于高通量检测。全基因组遗传分析的最新进展应能更全面地了解 RA 严重程度的相关基因。这些知识可以与现有的生物标志物一起,针对有不良放射学结局风险的患者进行靶向治疗。

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