Department of Orthopaedic Surgery and Sports Medicine, University of Kentucky, Lexington, Kentucky, USA.
Department of Orthopaedic Surgery, Brigham and Women's Hospital/Harvard Medical School, Boston, Massachusetts, USA.
J Orthop Res. 2023 Feb;41(2):300-306. doi: 10.1002/jor.25355. Epub 2022 May 13.
Anterior cruciate ligament (ACL) injury initiates a biochemical cascade thought to contribute to the onset and progression of posttraumatic osteoarthritis (PTOA). Interleukin-1ß (IL-1ß), IL-6, and C-telopeptide fragments of type II collagen (CTX-II) are implicated in joint inflammation and cartilage degradation following ACL injury; however, their association with pain is still being explored. The purpose of this study was to evaluate the associations between synovial fluid concentrations of IL-1ß, IL-6, and CTX-II with pain following ACL injury and reconstruction. We hypothesized that greater IL-1ß, IL-6, and CTX-II would correlate with greater Pain Visual Analogue Scale (VAS) scores. This was a secondary analysis of 23 patients (mean age = 18.4 years, BMI = 27.4, 13 females/10 males) with acute ACL tears who participated in a pilot randomized trial. Synovial fluid and VAS scores were collected on the day of initial presentation, at ACL reconstruction, and 1 and 4 weeks after surgery. Synovial fluid concentrations of IL-1ß, IL-6, and CTX-II were assessed using enzyme-linked immunoabsorbent assays, and repeated measures correlations were used to assess the relationships between pain and synovial IL-1ß, IL-6, or CTX-II after ACL injury and reconstruction. Pain was positively correlated with synovial fluid IL-6 concentrations (r = 0.52, p < 0.001); however, pain was inversely correlated with CTX-II (r = -0.39, p = 0.002). IL-1ß had no significant correlation with pain. Statement of clinical relevance: PTOA has been described as a "silent killer" and these results suggest that early PTOA may have pro-inflammatory pathways that are not primarily associated with pain but still lead to progressive cartilage loss.
前交叉韧带(ACL)损伤引发的生化级联反应被认为是导致创伤后骨关节炎(PTOA)发生和进展的原因。白细胞介素 1β(IL-1β)、IL-6 和 II 型胶原 C 端肽片段(CTX-II)在 ACL 损伤后关节炎症和软骨降解中起作用;然而,它们与疼痛的关系仍在探索中。本研究旨在评估 ACL 损伤和重建后滑液中 IL-1β、IL-6 和 CTX-II 与疼痛之间的关系。我们假设,IL-1β、IL-6 和 CTX-II 浓度越高,疼痛视觉模拟评分(VAS)越高。这是一项对 23 名急性 ACL 撕裂患者(平均年龄 18.4 岁,BMI 为 27.4,13 名女性/10 名男性)的二次分析,他们参加了一项先导随机试验。在初次就诊、ACL 重建时以及手术后 1 周和 4 周采集滑液和 VAS 评分。采用酶联免疫吸附试验测定滑液中 IL-1β、IL-6 和 CTX-II 的浓度,采用重复测量相关性分析评估 ACL 损伤和重建后疼痛与滑膜 IL-1β、IL-6 或 CTX-II 之间的关系。疼痛与滑液 IL-6 浓度呈正相关(r=0.52,p<0.001);然而,疼痛与 CTX-II 呈负相关(r=-0.39,p=0.002)。IL-1β 与疼痛无显著相关性。临床意义陈述:PTOA 被描述为一种“沉默杀手”,这些结果表明,早期 PTOA 可能有促炎途径,这些途径与疼痛没有主要关联,但仍会导致进行性软骨丧失。