Menzies Research Institute, University of Tasmania, Hobart, Australia.
Osteoarthritis Cartilage. 2010 Nov;18(11):1441-7. doi: 10.1016/j.joca.2010.08.016. Epub 2010 Sep 16.
The role of inflammation in osteoarthritis (OA) pathogenesis is unclear, and the associations between inflammatory cytokines and cartilage loss have not been reported. We determined the associations between serum levels of interleukin (IL)-6 and tumor necrosis factor-α (TNF-α), knee radiographic OA (ROA) and cartilage loss over 2.9 years in older adults.
A total of 172 randomly selected subjects (mean 63 years, range 52-78, 47% female) were studied at baseline and approximately 3 (range 2.6-3.3) years later. IL-6 and TNF-α were assessed by radioimmunoassay. T1-weighted fat-suppressed magnetic resonance imaging of the right knee was performed at baseline and follow-up to determine knee cartilage volume. Knee ROA of both knees was assessed at baseline.
At baseline, quartiles of IL-6 and TNF-α were associated with increased prevalence of medial tibiofemoral joint space narrowing (OARSI grade ≥ 1) in multivariate analyses [odds ratio (OR): 1.42 and 1.47 per quartile, respectively, both P<0.05]. Longitudinally, baseline IL-6 predicted loss of both medial and lateral tibial cartilage volume (β: -1.19% and -1.35% per annum per quartile, P<0.05 and P<0.01, respectively), independently of TNF-α. Change in IL-6 was associated with increased loss of medial and lateral tibial cartilage volume (β: -1.18% and -1.06% per annum per quartile, both P<0.05) and change in TNF-α was also negatively associated with change in medial cartilage volume (β: -1.27% per annum per quartile, P<0.05).
Serum levels of IL-6 and TNF-α are associated with knee cartilage loss in older people suggesting low level inflammation plays a role in the pathogenesis of knee OA.
炎症在骨关节炎(OA)发病机制中的作用尚不清楚,且炎症细胞因子与软骨丢失之间的关系尚未见报道。我们旨在确定白细胞介素(IL)-6 和肿瘤坏死因子(TNF)-α 血清水平与老年人膝关节放射学 OA(ROA)和软骨丢失之间的关系。
本研究共纳入 172 名随机选择的受试者(平均年龄 63 岁,范围 52-78 岁,47%为女性),分别在基线和大约 3 年后(范围 2.6-3.3 年)进行了研究。采用放射免疫法测定 IL-6 和 TNF-α。在基线和随访时对右膝关节进行 T1 加权脂肪抑制磁共振成像,以确定膝关节软骨体积。在基线时评估双侧膝关节 ROA。
在基线时,IL-6 和 TNF-α 的四分位区间与多变量分析中内侧胫骨股骨关节间隙狭窄(OARSI 分级≥1)的患病率增加相关[四分位区间每增加 1 个,比值比(OR)分别为 1.42 和 1.47,均 P<0.05]。纵向分析显示,基线 IL-6 可预测内侧和外侧胫骨软骨体积的丢失(四分位区间每增加 1 个,每年分别减少 1.19%和 1.35%,P<0.05 和 P<0.01),且独立于 TNF-α。IL-6 的变化与内侧和外侧胫骨软骨体积的丢失增加相关(四分位区间每增加 1 个,每年分别减少 1.18%和 1.06%,均 P<0.05),TNF-α 的变化也与内侧软骨体积的变化呈负相关(四分位区间每增加 1 个,每年减少 1.27%,P<0.05)。
血清 IL-6 和 TNF-α 水平与老年人膝关节软骨丢失相关,提示低度炎症在膝关节 OA 的发病机制中起作用。