Musculoskeletal Research Group, Institute of Cellular Medicine, Newcastle University, NE2 4HH, UK.
Semin Cell Dev Biol. 2017 Feb;62:57-66. doi: 10.1016/j.semcdb.2016.04.017. Epub 2016 Apr 26.
Osteoarthritis (OA) is a chronic musculoskeletal disease characterised by the destruction of articular cartilage, synovial inflammation and bone remodelling. Disease aetiology is complex and highly heritable, with genetic variation estimated to contribute to 50% of OA occurrence. Epigenetic alterations, including DNA methylation changes, have also been implicated in OA pathophysiology. This review examines what genetic and DNA methylation studies have taught us about the genes and pathways involved in OA pathology. The influence of DNA methylation on the molecular mechanisms underlying OA genetic risk and the consequence of this interaction on disease susceptibility and penetrance are also discussed.
骨关节炎(OA)是一种慢性肌肉骨骼疾病,其特征为关节软骨破坏、滑膜炎症和骨重塑。疾病发病机制复杂且高度遗传,遗传变异估计占 OA 发病的 50%。表观遗传改变,包括 DNA 甲基化改变,也与 OA 病理生理学有关。这篇综述探讨了关于 OA 病理的基因和途径,基因和 DNA 甲基化研究告诉了我们什么。还讨论了 DNA 甲基化对 OA 遗传风险潜在分子机制的影响,以及这种相互作用对疾病易感性和外显率的影响。