LREPR-EA3886, Evry-Génopole, université d'Evry-Val-d'Essonne, Evry, France.
Joint Bone Spine. 2009 Dec;76(6):602-7. doi: 10.1016/j.jbspin.2009.10.002.
Rheumatology deals with many different entities among which dys/autoimmune diseases occupy a position of preponderance. This review focuses on the concept of complex genetic disease, which is illustrated by three different chronic inflammatory joint diseases: rheumatoid arthritis, systemic lupus erythematosus, and systemic sclerosis. Genetic studies have established that a common genetic background is shared by many autoimmune disorders. Interestingly, although common genetic factors are shared by diseases that produce different phenotypes, risk variants can exert a strong influence on the phenotype of a given disease. Genetics cannot fully explain the determinism of complex genetic diseases. Future genetic studies must incorporate data on exposure to potential environmental factors. The next step in unravelling complex genetic diseases will involve investigations not only of gene-gene and gene-environment interactions, but also of epigenetics, defined as transmissible and reversible changes in gene expression that are not related to changes in the DNA sequence. The past decade has witnessed an impressive accumulation of data on the determinism of complex diseases, and the next will probably bring further insights into the pathophysiology of dys/autoimmune diseases.
风湿病学涉及许多不同的实体,其中自身免疫/失调疾病占据主导地位。这篇综述重点介绍了复杂遗传疾病的概念,并用三种不同的慢性炎症性关节疾病:类风湿关节炎、系统性红斑狼疮和系统性硬化症进行了说明。遗传研究已经证实,许多自身免疫性疾病具有共同的遗传背景。有趣的是,尽管产生不同表型的疾病具有共同的遗传因素,但风险变异可以对特定疾病的表型产生强烈影响。遗传学不能完全解释复杂遗传疾病的决定因素。未来的遗传研究必须结合对潜在环境因素暴露的数据。揭示复杂遗传疾病的下一步将不仅涉及基因-基因和基因-环境相互作用的研究,还涉及到定义为可传递和可逆的基因表达变化的表观遗传学,这些变化与 DNA 序列的变化无关。过去十年见证了复杂疾病决定因素方面令人印象深刻的数据积累,而下一个十年可能会进一步深入了解自身免疫/失调疾病的病理生理学。