Huang Shiqian, Chen Jiawei, Zhang Hao, Wu Wenjing, Xue Song, Zhu Zhaohua, Ding Changhai
Clinical Research Centre, Zhujiang Hospital, Southern Medical University, Guangzhou, China.
The Second School of Clinical Medicine, Zhujiang Hospital, Southern Medical University, Guangzhou, China.
Osteoarthr Cartil Open. 2025 Apr 26;7(2):100614. doi: 10.1016/j.ocarto.2025.100614. eCollection 2025 Jun.
Osteoarthritis (OA), a debilitating disease, has been recognized as a heterogenous disease, with metabolic syndrome-associated osteoarthritis (MetS-OA) emerging as a significant area of interest. Currently, the understanding of MOA remains limited, with a prevailing consensus attributing its etiology to the core components of metabolic syndrome: obesity, hyperglycemia, dyslipidemia, and hypertension. The aim of this review is to summarize the current understanding of the complex relationship between metabolic syndrome and OA from the perspectives of epidemiology and molecular biology, and to explore potential targeting strategies for metabolic syndrome in MetS-OA management.
This narrative review evaluated literature (2010-2024) from PubMed, examining clinical and mechanistic evidence linking metabolic syndrome to OA, including therapeutic studies targeting MetS-OA.
Metabolic syndrome aggravate the cartilage injury in MetS-OA through metabolic biomarkers (adipokines, advanced glycation end-products and oxidized LDL), metabolic responses (oxidative stress, insulin resistance and ischemic hypoxic injuries), and abnormally activated cells (adipocytes and macrophages). It ultimately lead to the aggravation of synovitis in MetS-OA through inflammatory mediators.
The exploration of the relationship between metabolic syndrome and OA could benefit the development of targeting strategies for MetS-OA, including currently FDA-approved drugs for the treatment of metabolic syndrome and potential drugs targeting metabolic factors, which might provide a novel avenue for the future management of MetS-OA.
骨关节炎(OA)是一种使人衰弱的疾病,已被认为是一种异质性疾病,其中代谢综合征相关骨关节炎(MetS-OA)成为一个重要的研究领域。目前,对MetS-OA的理解仍然有限,普遍的共识是将其病因归因于代谢综合征的核心组成部分:肥胖、高血糖、血脂异常和高血压。本综述的目的是从流行病学和分子生物学的角度总结目前对代谢综合征与OA之间复杂关系的理解,并探讨在MetS-OA管理中针对代谢综合征的潜在靶向策略。
本叙述性综述评估了来自PubMed的文献(2010 - 2024年),研究了将代谢综合征与OA联系起来的临床和机制证据,包括针对MetS-OA的治疗研究。
代谢综合征通过代谢生物标志物(脂肪因子、晚期糖基化终产物和氧化低密度脂蛋白)、代谢反应(氧化应激、胰岛素抵抗和缺血缺氧损伤)以及异常激活的细胞(脂肪细胞和巨噬细胞)加重MetS-OA中的软骨损伤。它最终通过炎症介质导致MetS-OA中滑膜炎的加重。
探索代谢综合征与OA之间的关系可能有益于MetS-OA靶向策略的开发,包括目前美国食品药品监督管理局(FDA)批准的用于治疗代谢综合征的药物以及针对代谢因子的潜在药物,这可能为未来MetS-OA的管理提供一条新途径。