Yang Rong-Sen, Chan Ding-Cheng, Chung Yao-Pang, Liu Shing-Hwa
Department of Orthopedics, College of Medicine and Hospital, National Taiwan University, Taipei 100, Taiwan.
Department of Geriatrics and Gerontology, College of Medicine and Hospital, National Taiwan University, Taipei 100, Taiwan.
Int J Mol Sci. 2025 Feb 13;26(4):1567. doi: 10.3390/ijms26041567.
Chronic kidney disease (CKD) is a significant public health concern. Osteoarthritis (OA), a common form of arthritis, has been shown to have a dramatically increased prevalence, particularly among individuals aged 40-50 and older, in the presence of CKD. Furthermore, CKD may exacerbate the progression and impact of OA. A survey study revealed that 53.9% of CKD patients undergoing long-term hemodialysis were diagnosed with OA. These findings underscore the potential association between CKD and OA. Uremic toxins, such as indoxyl sulfate, p-cresyl sulfate, transforming growth factor-β, and advanced glycation end-products, are regarded as potential risk factors in various CKD-related conditions, affecting bone and joint metabolism. However, whether these factors serve as a bridging mechanism between CKD and OA comorbidities, as well as their detailed roles in this context, remains unclear. Addressing the progression of OA in CKD patients and identifying effective treatment and prevention strategies is an urgent challenge that warrants immediate attention. This review focuses on describing and discussing the molecular pathological mechanisms underlying CKD-associated OA and the possible therapeutic strategies.
慢性肾脏病(CKD)是一个重大的公共卫生问题。骨关节炎(OA)是一种常见的关节炎形式,研究表明,在患有CKD的情况下,其患病率显著增加,尤其是在40至50岁及以上的人群中。此外,CKD可能会加剧OA的进展和影响。一项调查研究显示,接受长期血液透析的CKD患者中有53.9%被诊断患有OA。这些发现强调了CKD与OA之间的潜在关联。尿毒症毒素,如硫酸吲哚酚、对甲酚硫酸盐、转化生长因子-β和晚期糖基化终产物,被认为是各种CKD相关病症的潜在危险因素,影响骨骼和关节代谢。然而,这些因素是否作为CKD与OA合并症之间的桥梁机制,以及它们在这种情况下的详细作用,仍不清楚。应对CKD患者OA的进展并确定有效的治疗和预防策略是一项紧迫的挑战,值得立即关注。本综述重点描述和讨论CKD相关OA的分子病理机制以及可能的治疗策略。