Department of Rheumatology, Guy's Hospital, Great Maze Pond, London, UK.
Best Pract Res Clin Rheumatol. 2011 Aug;25(4):447-68. doi: 10.1016/j.berh.2011.10.010.
Rheumatoid arthritis (RA) is considered to occur when genetic and environmental factors interact to trigger immunopathological changes and consequently an inflammatory arthritis. Over the last few decades, epidemiological and genetic studies have identified a large number of risk factors for RA development, the most prominent of which comprise cigarette smoking and the shared epitope alleles. These risks appear to differ substantially between anti-cyclic citrullinated peptide (ACPA)-positive and ACPA-negative disease. In this article, we will summarise the risk factors for RA development that have currently been identified, outlining the specific gene-environment and gene-gene interactions that may occur to precipitate and perpetuate autoimmunity and RA. We will also focus on how this knowledge of risk factors for RA may be implemented in the future to identify individuals at a high risk of disease development in whom preventative strategies may be undertaken.
类风湿关节炎(RA)被认为是遗传和环境因素相互作用导致免疫病理变化,进而引发炎症性关节炎的结果。在过去的几十年中,流行病学和遗传学研究已经确定了大量 RA 发病的危险因素,其中最突出的包括吸烟和共同表位等位基因。这些风险在 ACPA 阳性和 ACPA 阴性疾病之间似乎有很大的不同。在本文中,我们将总结目前已确定的 RA 发病危险因素,概述可能发生的特定基因-环境和基因-基因相互作用,以引发和持续自身免疫和 RA。我们还将重点关注如何将这些 RA 危险因素的知识应用于未来,以识别出疾病发展风险高的个体,从而可以采取预防策略。