Investigational drugs for the treatment of osteoarthritis, an update on recent developments

被引:66
作者
Zhu, Zhaohua [1 ]
Li, Jia [1 ]
Ruan, Guangfeng [1 ,2 ]
Wang, Guoliang [3 ]
Huang, Cibo [4 ]
Ding, Changhai [1 ,2 ,3 ]
机构
[1] Southern Med Univ, Zhujiang Hosp, Clin Res Ctr, Guangzhou, Guangdong, Peoples R China
[2] Anhui Med Univ, Affiliated Hosp 1, Dept Rheumatol & Immunol, Arthrit Res Inst, Hefei, Anhui, Peoples R China
[3] Univ Tasmania, Menzies Inst Med Res, Hobart, Tas, Australia
[4] Beijing Hosp, Dept Rheumatol & Immunol, Beijing, Peoples R China
关键词
ADAMTS; growth factors; inflammation; MMP inhibitors; osteoarthritis; pain; TNF-alpha inhibitors; subchondral bone; therapy; MATRIX-METALLOPROTEINASE INHIBITORS; REDUCES CARTILAGE DEGENERATION; VARIABLE DOMAIN IMMUNOGLOBULIN; PAINFUL KNEE OSTEOARTHRITIS; FIBROBLAST GROWTH FACTOR-18; NECROSIS-FACTOR-ALPHA; BONE-MARROW LESIONS; DOUBLE-BLIND; STRONTIUM RANELATE; HAND OSTEOARTHRITIS;
D O I
10.1080/13543784.2018.1539075
中图分类号
R9 [药学];
学科分类号
100702 [药剂学];
摘要
Introduction: Osteoarthritis (OA) is the leading cause of pain, loss of function, and disability among elderly, with the knee the most affected joint. It is a heterogeneous condition characterized by complex and multifactorial etiologies which contribute to the broad variation in symptoms presentation and treatment responses that OA patients present. This poses a challenge for the development of effective treatment on OA. Areas covered: This review will discuss recent development of agents for the treatment of OA, updating our previous narrative review published in 2015. They include drugs for controlling local and systemic inflammation, regulating articular cartilage, targeting subchondral bone, and relieving pain. Expert opinion: Although new OA drugs such as monoclonal antibodies have shown marked effects and favorable tolerance, current treatment options for OA remain limited. The authors believe there is no miracle drug that can be used for all OA patients'; treatment and disease stage is crucial for the effectiveness of drugs. Therefore, early diagnosis, phenotyping OA patients and precise therapy would expedite the development of investigational drugs targeting at symptoms and disease progression of OA.
引用
收藏
页码:881 / 900
页数:20
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