On the predictive utility of animal models of osteoarthritis

被引:131
作者
Malfait, Anne-Marie [1 ,2 ]
Little, Christopher B. [3 ]
机构
[1] Rush Univ, Med Ctr, Dept Med, Div Rheumatol, Chicago, IL 60612 USA
[2] Rush Univ, Med Ctr, Dept Biochem, Chicago, IL 60612 USA
[3] Univ Sydney, Royal N Shore Hosp, Raymond Purves Bone & Joint Res Labs, Kolling Inst Med Res,Inst Bone & Joint Res, St Leonards, NSW 2065, Australia
基金
英国医学研究理事会;
关键词
HIGH-FAT DIET; HARTLEY GUINEA-PIG; MATRIX-METALLOPROTEINASE INHIBITOR; SYMPTOMATIC KNEE OSTEOARTHRITIS; RANDOMIZED CONTROLLED-TRIAL; PLACEBO-CONTROLLED TRIAL; NITRIC-OXIDE SYNTHASE; SUBCHONDRAL BONE LOSS; RAT MODEL; ARTICULAR-CARTILAGE;
D O I
10.1186/s13075-015-0747-6
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
Animal models of osteoarthritis are extensively used for investigating disease pathways and for preclinical testing of novel therapies. Their predictive utility, however, has often been questioned, mainly because preclinical efficacy of novel therapeutics is poorly translated in clinical trials. In the current narrative review, we consider the preclinical models that were used to support undertaking clinical trials for disease-modifying osteoarthritis drugs, and compare outcomes between clinical and preclinical studies. We discuss this in light of the 1999 Food and Drug Administration draft guidelines for industry for use in the development of drugs, devices, and biological products intended for the treatment of osteoarthritis, which raised five considerations on the usefulness of osteoarthritis models. We systematically discuss what has been learnt regarding these five points since 1999, with emphasis on replicating distinct risk factors and subtypes of human osteoarthritis, and on comprehensive evaluation of the disease in animals, including pathology of all joint tissues, biomarker analysis, and assessment of pain and joint function. Finally, we discuss lessons learnt and propose some recommendations for how the evidence from preclinical research might be strengthened with a view to improving success in clinical translation.
引用
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页数:14
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