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Statin use and knee osteoarthritis progression: Results from a post-hoc analysis of the SEKOIA trial

Epidemiological and experimental studies have suggested that lipid disorders might be involved in the pathophysiology of knee osteoarthritis (OA). Studies assessing the effect of statins on knee OA progression have shown conflicting results. We investigated the impact of statin use on radiological p...

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Published in:Joint, bone, spine : revue du rhumatisme bone, spine : revue du rhumatisme, 2018-10, Vol.85 (5), p.609-614
Main Authors: Eymard, Florent, Parsons, Camille, Edwards, Mark H., Petit-Dop, Florence, Reginster, Jean-Yves, Bruyère, Olivier, Chevalier, Xavier, Cooper, Cyrus, Richette, Pascal
Format: Article
Language:English
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Summary:Epidemiological and experimental studies have suggested that lipid disorders might be involved in the pathophysiology of knee osteoarthritis (OA). Studies assessing the effect of statins on knee OA progression have shown conflicting results. We investigated the impact of statin use on radiological progression in patients with radiological and symptomatic knee OA. In total, 336 patients from the placebo arm of SEKOIA trial completed the 3-year follow-up and were included in this post-hoc analysis. Statin use was recorded at baseline interview. Minimal medial tibiofemoral joint space was measured on plain radiographs by an automated method at baseline and then annually. Radiologic progression was defined as joint space narrowing≥0.5mm over 3 years. Overall, 71 patients were statin users (21.1%). They had a higher BMI (31.1±5.3 vs. 29.3±5.2kg/m2, P=0.008), a higher sum of metabolic factors (≥3 factors: 43.7% vs 7.2%; P for trend30kg/m2) and cardiovascular diseases [relative risk 1.49 (95% CI: 1.10–2.02), P=0.010]. Among patients with knee OA, statin use was associated with radiological worsening over 3 years, regardless of other potential confounding factors (obesity, type 2 diabetes, hypertension, disease duration, symptom intensity and radiological severity).
ISSN:1297-319X
1778-7254
1778-7254
DOI:10.1016/j.jbspin.2017.09.014