Abstract

BackgroundOsteoarthritis (OA) leads to joint failure and total joint replacement (TJR, either hip (H) or knee (K)). Worsening of pain and joint space narrowing are believed to be surrogates for joint failure; however, we hypothesize that TJR, as a reflection of joint failure, can be used as an endpoint in event-driven clinical trials within a reasonable duration. We explored the incidence of TJR in the Prospective Epidemiologic Risk Factor (PERF I) study.MethodsA total of 5855 Danish postmenopausal women aged 49–88 enrolled in the PERF I study during 1999–2001 (baseline). Three-, six- and twelve-year follow-up data from the Danish National Patient Registry was collected, including occurrence of TJR and OA diagnosis. At baseline the women were asked whether they had OA.ResultsThe women with a TJR diagnosis before or after baseline were on average 1 year older (p < 0.001) and heavier (p < 0.001), compared to women with no TJR. The 3-, 6- and 12-year cumulative incidences were 1.1, 2.4 and 6.0% for TKR, and 2.1, 4.4 and 9.3% for THR. For those with an OA diagnosis at baseline the respective incidences were 2.7, 5.6 and 11.7% and 3.9, 7.2 and 13.6%ConclusionsWithin 3, 6 or 12 years TJR incidences were double for women with an OA diagnosis compared to the all-comer population. TJRs are frequent amongst elderly women with OA and it is, therefore, feasible to conduct event-driven clinical trials where TJR is the endpoint demonstrating clinical benefit of a novel disease-modifying OA drug (DMOAD).

Highlights

  • Osteoarthritis (OA) is the most common form of arthritis, affecting about 10% of the world’s population [1]; without effective disease-modifying OA drugs (DMOADs) [2]

  • A total of 5855 postmenopausal women were included in the Prospective Epidemiologic Risk Factor (PERF) I study that were previously described by Neergaard et al [16]

  • Of the women enrolled in PERF I, 430 women had a total of 566 total knee replacements (TKR), 786 women had a total of 985 total hip replacements (THR) and 1106 women had either a TKR or a THR until end of study

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Summary

Introduction

Osteoarthritis (OA) is the most common form of arthritis, affecting about 10% of the world’s population [1]; without effective disease-modifying OA drugs (DMOADs) [2]. It is well accepted that the lack of DMOADs is partly due to the heterogeneity of OA, associated with a lack of effective enrichment strategies for clinical trial design [3, 4]. OA progression can span several decades, have periods of rapid progression leading to joint failure and total joint replacement (TJR). The lack of clear clinical phenotypes and subgrouping tools results in large drug trials with expectations of marginal significant effect size. X-ray (e.g. Osteoarthritis (OA) leads to joint failure and total joint replacement (TJR, either hip (H) or knee (K)). We explored the incidence of TJR in the Prospective Epidemiologic Risk Factor (PERF I) study

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