Emerging therapeutic agents in osteoarthritis

被引:37
作者
Jose Alcaraz, Maria [1 ]
Isabel Guillen, Maria [1 ,2 ]
Luisa Ferrandiz, Maria [1 ]
机构
[1] Univ Valencia, Univ Politecn Valencia, Inst Interuniv Invest Reconocimiento Mol & Desarr, Av Vicent A Estelles S-N, E-46100 Valencia, Spain
[2] Cardenal Herrera CEU Univ, Dept Pharm, Valencia 46115, Spain
关键词
Osteoarthritis; Pain; Inflammatory mediators; Structural alterations; Nerve growth factor; Wnt; ADAMTS; Cathepsin K; Fibroblast growth factor-18; Cellular therapy; NERVE GROWTH-FACTOR; MESENCHYMAL STEM-CELLS; VARIABLE DOMAIN IMMUNOGLOBULIN; VASCULAR ADHESION PROTEIN-1; SENSITIVE AMINE-OXIDASE; DOUBLE-BLIND; KNEE OSTEOARTHRITIS; ARTICULAR-CARTILAGE; INTRAARTICULAR SPRIFERMIN; TRPV1; ANTAGONIST;
D O I
10.1016/j.bcp.2019.02.034
中图分类号
R9 [药学];
学科分类号
100702 [药剂学];
摘要
Osteoarthritis (OA) is the most common joint disorder and a leading cause of disability. Current treatments for OA can improve symptoms but do not delay the progression of disease. In the last years, much effort has been devoted to developing new treatments for OA focused on pain control, inflammatory mediators or degradation of articular tissues. Although promising results have been obtained in ex vivo studies and animal models of OA, few of these agents have completed clinical trials. Available clinical data support the interest of nerve growth factor as a target in pain control as well as the disease-modifying potential of inhibitors of Wnt signaling or catabolic enzymes such as aggrecanases and cathepsin K, and anabolic strategies like fibroblast growth factor-18 or cellular therapies. Carefully controlled studies in patients selected according to OA phenotypes and with a long follow-up will help to confirm the relevance of these new approaches as emerging therapeutic treatments in OA.
引用
收藏
页码:4 / 16
页数:13
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