Department of Pathophysiology, Biomedicine and Translational medicine, University of Tartu, Tartu, Estonia; Department of Traumatology and Orthopaedics, Tartu University Hospital, Tartu, Estonia.
Department of Traumatology and Orthopaedics, Tartu University Hospital, Tartu, Estonia; Clinic of Traumatology and Orthopaedics, Tartu University Hospital, Tartu, Estonia.
Adv Clin Chem. 2021;100:37-90. doi: 10.1016/bs.acc.2020.04.002. Epub 2020 May 29.
A sharp rise in osteoarthritis (OA) incidence is expected as over 25% of world population ages in the coming decade. Although OA is considered a degenerative disease, mounting evidence suggests a strong connection with chronic metabolic conditions and low-grade inflammation. OA pathology is increasingly understood as a complex interplay of multiple pathological events including oxidative stress, synovitis and immune responses revealing its intricate nature. Cellular, biochemical and molecular aspects of these pathological events along with major outcomes of the relevant research studies in this area are discussed in the present review. With reference to their published and unpublished work, the authors strongly propose synovitis as a central OA pathology and the key OA pathological events are described in connection with it. Recent research outcomes also have succeeded to establish a linkage between metabolic syndrome and OA, which has been precisely included in the present review. Impact of aging process cannot be neglected in OA. Cell senescence is an important mechanism of aging through which it facilitates development of OA like other degenerative disorders, also discussed within a frame of OA. Conclusively, the reviewers urge low-grade inflammation linked to aging and derailed immune function as a pathological platform for OA development and progression. Thus, interventions targeted to prevent inflammaging hold a promising potential in effective OA management and efforts should be invested in this direction.
骨关节炎 (OA) 的发病率预计会急剧上升,因为在未来十年中,全球超过 25%的人口将老龄化。尽管 OA 被认为是一种退行性疾病,但越来越多的证据表明它与慢性代谢性疾病和低度炎症密切相关。OA 病理学越来越被理解为多种病理事件的复杂相互作用,包括氧化应激、滑膜炎和免疫反应,揭示了其复杂的性质。本综述讨论了这些病理事件的细胞、生化和分子方面以及该领域相关研究的主要结果。作者参考他们已发表和未发表的工作,强烈提出滑膜炎是 OA 的核心病理学,并描述了与滑膜炎相关的关键 OA 病理事件。最近的研究结果还成功地建立了代谢综合征与 OA 之间的联系,这在本综述中也有详细介绍。OA 过程中不能忽视老化过程的影响。细胞衰老通过促进 OA 的发展,是衰老的一个重要机制,这在 OA 的框架内也进行了讨论。总之,评论员敦促将与衰老相关的低度炎症和免疫功能失调视为 OA 发展和进展的病理平台。因此,针对预防炎症衰老的干预措施在 OA 的有效管理中具有很大的潜力,应该朝着这个方向投入努力。
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