Institute of Ageing and Chronic Disease, University of Liverpool, William Henry Duncan Building, West Derby Road, Liverpool, L7 8TX, UK.
Department of Physiology, School of Medicine, REMEDI, NUI Galway, Human Biology Building, University Road, Galway, Ireland.
Curr Rheumatol Rep. 2019 Jun 15;21(8):40. doi: 10.1007/s11926-019-0839-4.
Osteoarthritis (OA) is a subset of joint disorders resulting in degeneration of synovial joints. This leads to pain, disability and loss of independence. Knee and hip OA are extremely prevalent, and their occurrence increases with ageing. Similarly, loss of muscle mass and function, sarcopenia, occurs during ageing.
Little is known about the impact of muscle wasting on OA progression; nevertheless, it has been suggested that muscle wasting directly affects the stability of the joints and loss of mobility leads to gradual degeneration of articular cartilage. The molecular mechanisms underlying muscle wasting in OA are not well understood; however, these are probably related to changes in gene expression, as well as epigenetic modifications. It is becoming clear that skeletal muscle wasting plays an important role in OA development and/or progression. Here, we discuss mechanisms, current interventions, such as exercise, and potentially novel approaches, such as modulation of microRNAs, aiming at ameliorating OA symptoms through maintaining muscle mass and function.
骨关节炎(OA)是关节疾病的一个分支,导致滑膜关节退化。这会导致疼痛、残疾和丧失独立性。膝关节和髋关节 OA 极为普遍,且随着年龄的增长其发生率会增加。同样,肌肉质量和功能的丧失,即肌肉减少症,也会随着年龄的增长而发生。
关于肌肉减少对 OA 进展的影响知之甚少;然而,有人认为肌肉减少症直接影响关节的稳定性,而活动能力的丧失会导致关节软骨逐渐退化。OA 中肌肉减少的分子机制尚不清楚;然而,这些机制可能与基因表达的变化以及表观遗传修饰有关。越来越清楚的是,骨骼肌减少在 OA 的发展和/或进展中起着重要作用。在这里,我们讨论了机制、目前的干预措施,如运动,以及潜在的新方法,如 microRNAs 的调节,旨在通过维持肌肉质量和功能来改善 OA 症状。