Patel Sagar, Foster Cameron, Patel Kamal, Hunter Monte, Isales Carlos M, Fulzele Sadanand
Department of Medicine, Augusta University, Augusta, GA 30912, USA.
Department of Orthopaedic Surgery, College of Medicine, University of Florida, Jacksonville, FL 32209, USA.
Int J Mol Sci. 2025 Sep 3;26(17):8569. doi: 10.3390/ijms26178569.
The COVID-19 pandemic has revealed significant secondary complications affecting musculoskeletal (MSK) health, especially in patients with pre-existing conditions. This review synthesizes data from clinical and experimental studies on key MSK biomarkers, including cartilage oligomeric matrix protein (COMP), hyaluronic acid (HA), osteocalcin, alkaline phosphatase (ALP), procollagen type I N-terminal peptide (PINP), osteopontin (OPN), matrix metalloproteinases (MMP-3 and MMP-9), myostatin, IGF-1, follistatin, and creatine kinase. COVID-19 is associated with decreased COMP and osteocalcin levels, indicating cartilage degradation and impaired bone formation, alongside elevated HA, ALP, PINP, OPN, and MMPs, reflecting increased joint inflammation, bone remodeling, and tissue breakdown. Changes in myostatin, IGF-1, follistatin, and creatine kinase levels have been shown to be linked with COVID-19-related sarcopenia. These biomarker alterations provide insight into the underlying mechanisms of MSK damage in COVID-19 patients and highlight the potential for using these markers in early diagnosis and management of post-COVID musculoskeletal disorders. Further longitudinal research is essential to develop targeted therapies aimed at mitigating long-term MSK complications in affected individuals.
新冠疫情已揭示出影响肌肉骨骼(MSK)健康的重大继发性并发症,尤其是在患有基础疾病的患者中。本综述综合了关于关键MSK生物标志物的临床和实验研究数据,这些生物标志物包括软骨寡聚基质蛋白(COMP)、透明质酸(HA)、骨钙素、碱性磷酸酶(ALP)、I型前胶原N端肽(PINP)、骨桥蛋白(OPN)、基质金属蛋白酶(MMP - 3和MMP - 9)、肌肉生长抑制素、胰岛素样生长因子-1(IGF - 1)、卵泡抑素和肌酸激酶。新冠病毒感染与COMP和骨钙素水平降低有关,表明软骨降解和骨形成受损,同时HA、ALP、PINP、OPN和基质金属蛋白酶水平升高,反映出关节炎症增加、骨重塑和组织分解。肌肉生长抑制素、IGF - 1、卵泡抑素和肌酸激酶水平的变化已被证明与新冠病毒感染相关的肌肉减少症有关。这些生物标志物的改变为了解新冠患者MSK损伤的潜在机制提供了线索,并突出了在新冠后肌肉骨骼疾病的早期诊断和管理中使用这些标志物的潜力。进一步的纵向研究对于开发旨在减轻受影响个体长期MSK并发症的靶向治疗至关重要。