Wasilko Scott M, Tourville Timothy W, DeSarno Michael J, Slauterbeck James R, Johnson Robert J, Struglics André, Beynnon Bruce D
Department of Orthopaedics & Rehabilitation, University of Vermont College of Medicine, Burlington, Vermont.
Department of Medical Biostatistics, University of Vermont, Burlington, Vermont.
J Orthop Res. 2016 May;34(5):820-7. doi: 10.1002/jor.23084. Epub 2015 Nov 25.
Anterior cruciate ligament (ACL) trauma often occurs in combination with injury to the articular cartilage of the knee, this can result in earlier radiographic evidence of post traumatic osteoarthritis (OA) of the knee compared to the contralateral, ACL intact knee; however, the biomechanical and biological mechanisms associated with the onset and progression of this disease are not understood. We sought to gain insight into the mechanisms by determining the relationship between articular cartilage injury associated with ACL trauma and the expression of synovial fluid biomarkers of articular cartilage metabolism, and to evaluate the relationship between these biomarkers and the patient's perspective of the outcomes. Synovial fluid samples were acquired from 39 ACL injured subjects at an average of 10 weeks after injury, and 32 control subjects with normal knees (documented with clinical exam and MRI assessment). Subjects in the ACL-injured group were classified as low-risk for future OA if they displayed an International Cartilage Repair Society (ICRS) Grade 2 articular cartilage lesion or less and high-risk for future OA if they had an ICRS Grade 3A articular cartilage lesion. The patient's perspective of the injury was evaluated with the Knee Injury and Osteoarthritis Outcomes Score (KOOS). There were no significant differences in mean concentrations of the markers of type II collagen metabolism (CPII, C2C, and C1,2C) or the aggrecan breakdown Alanine-Arginine-Glycine-Serine (ARGS) -fragment between control subjects and the subjects in the low- and high-risk groups (p-value range: 0.80-0.43). Associations between ARGS-aggrecan concentration and KOOS subscales of symptoms and pain were significantly different between the low- and high-risk groups (p = 0.03 and p = 0.01, respectively). Likewise, there was strong evidence in support of an association between the markers of type II collagen metabolism (C1,2C and CPII concentrations) and the KOOS subscale of pain between the low- and high-risk groups (p = 0.051 and 0.077, correspondingly). In ACL injured subjects with concomitant Grade 3A articular cartilage injuries, concentrations of synovial fluid ARGS-aggrecan were directly associated with improvements in KOOS symptoms and pain. These findings suggest the possible involvement of ARGS-aggrecan in a localized tissue repair response involving an increase in aggrecan turnover following severe knee trauma. © 2015 Orthopaedic Research Society. Published by Wiley Periodicals, Inc. J Orthop Res 34:820-827, 2016.
前交叉韧带(ACL)损伤常与膝关节软骨损伤同时发生,与对侧ACL完整的膝关节相比,这会导致膝关节创伤后骨关节炎(OA)的影像学证据出现得更早;然而,与这种疾病的发生和发展相关的生物力学和生物学机制尚不清楚。我们试图通过确定与ACL损伤相关的关节软骨损伤与关节软骨代谢的滑液生物标志物表达之间的关系,来深入了解其机制,并评估这些生物标志物与患者对治疗结果的看法之间的关系。在平均受伤10周后,从39名ACL损伤患者以及32名膝关节正常的对照受试者(通过临床检查和MRI评估记录)中采集滑液样本。ACL损伤组的受试者如果表现为国际软骨修复协会(ICRS)2级或更低级别的关节软骨损伤,则被归类为未来OA的低风险组;如果有ICRS 3A级关节软骨损伤,则被归类为未来OA的高风险组。通过膝关节损伤和骨关节炎疗效评分(KOOS)评估患者对损伤的看法。在对照受试者与低风险和高风险组的受试者之间,II型胶原代谢标志物(CPII、C2C和C1,2C)或聚集蛋白聚糖分解产物丙氨酸 - 精氨酸 - 甘氨酸 - 丝氨酸(ARGS)片段的平均浓度没有显著差异(p值范围:0.80 - 0.43)。低风险和高风险组之间,ARGS - 聚集蛋白聚糖浓度与KOOS症状和疼痛子量表之间的关联存在显著差异(分别为p = 0.03和p = 0.01)。同样,有强有力的证据支持低风险和高风险组之间II型胶原代谢标志物(C1,2C和CPII浓度)与KOOS疼痛子量表之间存在关联(相应地为p = 0.051和0.077)。在伴有3A级关节软骨损伤的ACL损伤受试者中,滑液ARGS - 聚集蛋白聚糖浓度与KOOS症状和疼痛的改善直接相关。这些发现表明ARGS - 聚集蛋白聚糖可能参与了严重膝关节创伤后聚集蛋白聚糖周转增加的局部组织修复反应。© 2015骨科研究协会。由Wiley Periodicals, Inc.出版。《骨科研究杂志》34:820 - 827,2016年。