School of Public Health, Southern Medical University, Guangzhou, China.
School of Health Services Management, Southern Medical University, Guangzhou, China.
Cartilage. 2019 Oct;10(4):408-416. doi: 10.1177/1947603518764280. Epub 2018 Mar 22.
The CC chemokine family member eotaxin-1, also named chemokine C-C motif ligand 11 (CCL11), has been detected in knee osteoarthritis (OA) and could induce breakdown of cartilage matrix. This study was performed to investigate the plasma and synovial fluid eotaxin-1 levels with the disease progression in elderly Han Chinese with primary knee OA.
A total of 143 elderly primary knee OA patients and 135 healthy controls were enrolled in the study. The Western Ontario and McMaster Universities Arthritis Index (WOMAC) was performed to evaluate the clinical severity. The radiographic severity was assessed by Kellgren-Lawrence (K-L) grading. Plasma and synovial fluid (SF) eotaxin-1 levels were explored using enzyme-linked immunosorbent assay. The SF levels of matrix metalloproteinase-3 (MMP-3) and interleukin-6 (IL-6) were also examined.
Elevated plasma eotaxin-1 levels were found in knee OA patients compared with healthy controls. Eotaxin-1 levels in SF of knee OA patients with K-L grade 4 were significantly elevated compared with those with K-L grades 2 and 3. Meanwhile, knee OA patients with K-L grade 3 had significantly increased SF levels of eotaxin-1 compared with those with K-L grade 2. Plasma eotaxin-1 levels in different K-L grading did not reach significant difference. Eotaxin-1 levels in SF of knee OA patients were significantly associated with disease severity evaluated by KL grading criteria. In addition, eotaxin-1 levels in SF were positively related to clinical severity illustrated by WOMAC as well as biochemical markers MMP-3 and IL-6.
Eotaxin-1 levels in SF instead of plasma, were independently and positively related to the disease severity in elderly knee OA patients. The inhibition of eotaxin-1 and its related signaling pathways may serve as a novel therapeutic approach for OA progression.
CC 趋化因子家族成员嗜酸性粒细胞趋化因子-1(也称为趋化因子 C-C 基序配体 11,CCL11)已在膝骨关节炎(OA)中被检测到,并可诱导软骨基质的破坏。本研究旨在调查血浆和滑液嗜酸性粒细胞趋化因子-1(eotaxin-1)水平与老年汉族原发性膝骨关节炎患者疾病进展的关系。
共纳入 143 名老年原发性膝骨关节炎患者和 135 名健康对照者。采用西安大略和麦克马斯特大学骨关节炎指数(WOMAC)评估临床严重程度。采用 Kellgren-Lawrence(K-L)分级评估放射学严重程度。采用酶联免疫吸附试验(ELISA)检测血浆和滑液(SF)eotaxin-1 水平。还检测了 SF 基质金属蛋白酶-3(MMP-3)和白细胞介素-6(IL-6)的水平。
与健康对照组相比,膝骨关节炎患者的血浆 eotaxin-1 水平升高。K-L 分级 4 的膝骨关节炎患者的 SF eotaxin-1 水平明显高于 K-L 分级 2 和 3 的患者。同时,K-L 分级 3 的膝骨关节炎患者的 SF eotaxin-1 水平明显高于 K-L 分级 2 的患者。不同 K-L 分级的血浆 eotaxin-1 水平无显著差异。SF 中 eotaxin-1 水平与 K-L 分级标准评估的疾病严重程度显著相关。此外,SF 中 eotaxin-1 水平与 WOMAC 评估的临床严重程度以及生化标志物 MMP-3 和 IL-6 呈正相关。
SF 中的 eotaxin-1 水平而非血浆中的 eotaxin-1 水平与老年膝骨关节炎患者的疾病严重程度独立且呈正相关。抑制 eotaxin-1 及其相关信号通路可能成为 OA 进展的一种新的治疗方法。