Clinical and biochemical factors associated with risk of total joint replacement and radiographic progression in osteoarthritis: Data from two phase III clinical trials

被引:17
|
作者
Bihlet, Asger Reinstrup [1 ]
Bjerre-Bastos, Jonathan Jetsmark [1 ,2 ]
Andersen, Jeppe Ragnar [1 ]
Byrjalsen, Inger [1 ]
Karsdal, Morten Asser [3 ]
Bay-Jensen, Anne-Christine [3 ]
机构
[1] Nord Biosci Clin Dev, Herlev, Denmark
[2] Univ Copenhagen, Dept Biomed Sci, Ctr Hlth Aging, Copenhagen, Denmark
[3] Nord Biosci AS, Herlev, Denmark
关键词
Biomarkers; Joint replacement; Progression; KNEE OSTEOARTHRITIS; OUTCOME MEASURES; DOUBLE-BLIND; HIP; IDENTIFICATION; MULTICENTER; EFFICACY; MARKERS; SAFETY;
D O I
10.1016/j.semarthrit.2020.03.002
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objectives: Clinical trials of new disease-modifying treatments for osteoarthritis should demonstrate a positive effect on a functional outcome or reduction in joint failure in order to be considered successful. Total joint replacement (TJR) surgery may be considered as joint failure, but great variation in the incidence of TJR complicates its use as a study endpoint. Factors predicting elevated risk of TJR could potentially be used to enrich such outcome-trials. Methods: Using cumulative data from two phase three clinical trials with urine samples from 1255 knee OA patients followed for two years, we assessed the value of a series of baseline clinical variables including the uCTX-II biomarker, as predictors of joint-space narrowing, Kellgren-Lawrence-grade progression, and total joint replacement. Results: A prediction-model incorporating age, sex, BMI, CTX-II and KL-grade predicted TJR within the two-year period with an AUC of 0.75 (95% CI: 0.72-0.77). The participants with a cumulative KL-grade between knees of 5, 6, or 7 had a more than 3 times higher risk of TJR in the study period compared to lower (HR: 3.03, 95% CI: 1.54 to 5.96, p = 0.001). Age was associated with increased TJR risk (per 5 years of age: HR: 1.28, 95% CI: 1.03-3.79, p = 0.05). Baseline u-CTX-II was associated with elevated risk of radiographic progression in terms of both JSN and KL-grade. Conclusions: A composite model combining baseline age, sex, BMI, u-CTX-II and KL-grade was able to acceptably predict TJR during a two-year period. In the absence of baseline radiographic OA severity, u-CTX-II independently contributed to prediction of TJR. Baseline urine CTX-II was associated with risk of radiographic progression. (C) 2020 Elsevier Inc. All rights reserved.
引用
收藏
页码:1374 / 1381
页数:8
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