Department of Epidemiology and Preventive Medicine, School of Public Health and Preventive Medicine, Monash University, 553 St Kilda Road, Melbourne, VIC, 3004, Australia.
Medical Imaging Research & Development, ArthroLab Inc., Montreal, QC, Canada.
Arthritis Res Ther. 2018 Nov 6;20(1):250. doi: 10.1186/s13075-018-1751-4.
There is evidence that knee pain not only is a consequence of structural deterioration in osteoarthritis (OA) but also contributes to structural progression. Clarifying this is important because targeting the factors related to knee pain may offer a clinical approach for slowing the progression of knee OA. The aim of this study was to examine whether knee pain over 1 year predicted cartilage volume loss, incidence and progression of radiographic osteoarthritis (ROA) over 4 years.
Osteoarthritis Initiative participants with no ROA (Kellgren-Lawrence grade ≤ 1) (n = 2120) and with ROA (Kellgren-Lawrence grade > 2) (n = 2249) were examined. Knee pain was assessed at baseline and 1 year using the Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC). Knee pain patterns were categorised as no pain (WOMAC pain < 5 at baseline and 1 year), fluctuating pain (WOMAC pain > 5 at either time point) and persistent pain (WOMAC pain > 5 at both time points). Cartilage volume, incidence and progression of ROA were assessed using magnetic resonance imaging and x-rays at baseline and 4-years.
In both non-ROA and ROA, greater baseline WOMAC knee pain score was associated with increased medial and lateral cartilage volume loss (p ≤ 0.001), incidence (OR 1.07, 95% CI 1.01-1.13) and progression (OR 1.07, 95% CI 1.03-1.10) of ROA. Non-ROA and ROA participants with fluctuating and persistent knee pain had increased cartilage volume loss compared with those with no pain (p for trend ≤ 0.01). Non-ROA participants with fluctuating knee pain had increased risk of incident ROA (OR 1.62, 95% CI 1.04-2.54), corresponding to a number needed to harm of 19.5. In ROA the risk of progressive ROA increased in participants with persistent knee pain (OR 1.82, 95% CI 1.28-2.60), corresponding to a number needed to harm of 9.6.
Knee pain over 1 year predicted accelerated cartilage volume loss and increased risk of incident and progressive ROA. Early management of knee pain and controlling knee pain over time by targeting the underlying mechanisms may be important for preserving knee structure and reducing the burden of knee OA.
有证据表明,膝关节疼痛不仅是骨关节炎(OA)结构恶化的结果,而且还会导致结构进展。明确这一点很重要,因为针对与膝关节疼痛相关的因素可能为减缓膝关节 OA 的进展提供一种临床方法。本研究的目的是探讨膝关节疼痛在 1 年内是否会预测 4 年内软骨体积损失、放射学骨关节炎(ROA)的发生率和进展。
研究纳入了无 ROA(Kellgren-Lawrence 分级≤1)(n=2120)和有 ROA(Kellgren-Lawrence 分级>2)(n=2249)的骨关节炎倡议参与者。在基线和 1 年时使用 Western Ontario 和 McMaster 大学骨关节炎指数(WOMAC)评估膝关节疼痛。膝关节疼痛模式分为无疼痛(WOMAC 疼痛<5,基线和 1 年)、波动疼痛(WOMAC 疼痛在任何一个时间点均>5)和持续疼痛(WOMAC 疼痛在两个时间点均>5)。使用磁共振成像和 X 射线在基线和 4 年时评估软骨体积、ROA 的发生率和进展。
在非 ROA 和 ROA 中,基线 WOMAC 膝关节疼痛评分较高与内侧和外侧软骨体积损失增加(p≤0.001)、ROA 的发生率(OR 1.07,95%CI 1.01-1.13)和进展(OR 1.07,95%CI 1.03-1.10)相关。与无疼痛者相比,有波动和持续膝关节疼痛的非 ROA 和 ROA 参与者的软骨体积损失增加(p 趋势值≤0.01)。有波动膝关节疼痛的非 ROA 参与者发生 ROA 的风险增加(OR 1.62,95%CI 1.04-2.54),对应的危害人数为 19.5。在 ROA 中,持续膝关节疼痛的参与者发生进展性 ROA 的风险增加(OR 1.82,95%CI 1.28-2.60),对应的危害人数为 9.6。
1 年内的膝关节疼痛预测了软骨体积的加速损失以及发生和进展性 ROA 的风险增加。通过针对潜在机制早期管理膝关节疼痛并长期控制膝关节疼痛,可能对保持膝关节结构和减轻膝关节 OA 的负担很重要。