AI Article Synopsis

  • * Recent pharmacological research is focusing on preventive and early treatment strategies, exploring various biologic agents including DNA, noncoding RNA, exosomes, platelet-rich plasma (PRP), and proteins for their potential effects on OA.
  • * The review summarizes literature from January 2016 to August 2021 to provide a comprehensive understanding of pharmacological advances in OA intervention and aims to guide future research in this area.

Article Abstract

Osteoarthritis (OA) is a degenerative joint disease in the musculoskeletal system with a relatively high incidence and disability rate in the elderly. It is characterized by the degradation of articular cartilage, inflammation of the synovial membrane, and abnormal structure in the periarticular and subchondral bones. Although progress has been made in uncovering the molecular mechanism, the etiology of OA is still complicated and unclear. Nevertheless, there is no treatment method that can effectively prevent or reverse the deterioration of cartilage and bone structure. In recent years, in the field of pharmacology, research focus has shifted to disease prevention and early treatment rather than disease modification in OA. Biologic agents become more and more attractive as their direct or indirect intervention effects on the initiation or development of OA. In this review, we will discuss a wide spectrum of biologic agents ranging from DNA, noncoding RNA, exosome, platelet-rich plasma (PRP), to protein. We searched for key words such as OA, DNA, gene, RNA, exosome, PRP, protein, and so on. From the pharmacological aspect, stem cell therapy is a very special technique, which is not included in this review. The literatures ranging from January 2016 to August 2021 were included and summarized. In this review, we aim to help readers have a complete and precise understanding of the current pharmacological research progress in the intervention of OA from the biological aspect and provide an indication for the future translational studies.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8649959PMC
http://dx.doi.org/10.3389/fphar.2021.772678DOI Listing

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