The frequency and severity of ultrasound-detected osteoarthritis features in the knees and their associations with pain: Cross-sectional analyses of the Nor-Hand study
Caroline H. Dekkerhus , Alexander Mathiessen , Caroline M. Fjellstad , Barbara Slatwkosky-Christensen , Hilde Berner Hammer , Ida K. Haugen
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引用次数: 0
Abstract
Objective
To investigate the frequency and severity of ultrasound-detected osteophytes and synovitis in people with and without knee osteoarthritis (OA), and to explore the association between these ultrasound features and pain.
Design
In the Nor-Hand study, both knees were assessed for osteophytes (0–3 scale, four locations per knee) and grey-scale synovitis (0–3 scale). The frequency and severity of the ultrasound-detected features were compared in individuals with and without knee OA defined by the American College of Rheumatology criteria. Pain was self-reported in each knee (yes/no) and by the Western/Ontario McMaster University index (WOMAC). The associations between ultrasound-detected features and pain were examined by regression analyses adjusted for age, sex, and body mass index.
Results
We analyzed 286 participants. Osteophytes of all sizes were more common in participants with knee OA compared to those without (65.9 % vs. 40.8 %, p < 0.001). No between-group difference was found for the frequency of any grey-scale synovitis (45.5 % vs. 44.7 %, p = 0.67), while severe synovitis was more common in those with knee OA. Ultrasound-detected osteophyte sum score, but not synovitis, was associated with WOMAC pain (B = 0.18, 95 % CI 0.03–0.32). Osteophytes of all sizes were associated with pain in the same knee with odds ratio (OR, 95 % CI) ranging from 1.85 (1.20–2.84) to 9.02 (4.04–20.10). Statistically significant association was found for severe synovitis only (OR = 6.63, 95 % CI 2.26–19.43).
Conclusions
Ultrasound-detected osteophytes were prevalent in people with knee OA and were associated with pain. OA pathology in individuals without fulfilling the knee OA criteria may reflect early or subclinical OA.