iOrthoBiologix, Charlotte, NC.
Department of Physical Medicine and Rehabilitation, Virginia Commonwealth University Health System, Richmond, VA.
PM R. 2021 Jul;13(7):707-719. doi: 10.1002/pmrj.12561.
BACKGROUND: Platelet-rich-plasma (PRP) is used to treat knee osteoarthritis; however, mechanistic evidence of PRP effectiveness for pain relief is limited. OBJECTIVE: To assess molecular biomarkers and mesenchymal stem cells (MSCs) in synovial fluid during PRP treatment of the osteoarthritic knee joint. DESIGN: Single blinded, randomized, placebo controlled pilot study. SETTING: Veterans Affairs Medical Center. PARTICIPANTS: Seventeen participants with mild to moderate knee osteoarthritis were randomized in a 2:1 placebo-controlled ratio, receiving PRP or saline (placebo) intra-articular injection into the knee joint. METHODS: Knee synovial fluid was analyzed before the respective injections and again 10 days following injection. Participants were followed up to 12 months completing visual analog scale (VAS) and Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC) questionnaires at intervals over that period. MAIN OUTCOME MEASURES: The effects of PRP on synovial protein and MSC gene expression levels were measured by multiplex enzyme-linked immunosorbent assay and quantitative polymerase chain reaction. RESULTS: Novel biomarkers including levels of interleukin (IL)-5, IL-6, IL-10, and tumor necrosis factor-α were measured in synovial fluid 10 days after PRP treatment. Altered gene expression profiles in MSCs from patients treated with PRP were observed for matrix metalloproteinases and inflammatory markers (IL-6, IL-8, CCL2, TNF-α). A2M protease was significantly increased following PRP treatment (P = .005). WOMAC scores declined for up to 3 months from baseline levels and remained low at 6 and 12 months in the PRP group. In contrast, WOMAC scores for patients receiving the saline injection were relatively unchanged for up to 12 months. CONCLUSIONS: We report significant changes for the biomarker A2M (P = .005) as well as differences in expression of cellular markers and postulate that PRP modulates the local knee synovial environment by altering the inflammatory milieu, matrix degradation, and angiogenic growth factors. The PRP treatment group had less pain and stiffness and improved function scores.
背景:富含血小板的血浆 (PRP) 被用于治疗膝骨关节炎;然而,用于缓解疼痛的 PRP 有效性的机制证据有限。
目的:评估 PRP 治疗膝骨关节炎时滑液中的分子生物标志物和间充质干细胞 (MSCs)。
设计:单盲、随机、安慰剂对照的初步研究。
地点:退伍军人事务医疗中心。
参与者:17 名患有轻度至中度膝骨关节炎的参与者以 2:1 的安慰剂对照比例随机分组,接受 PRP 或关节内注射膝关节生理盐水 (安慰剂)。
方法:分别在各自注射前和注射后 10 天分析膝关节滑液。在那段时间内,参与者通过视觉模拟量表 (VAS) 和西部安大略省和麦克马斯特大学骨关节炎指数 (WOMAC) 问卷进行随访,在此期间每隔一段时间进行一次。
主要观察指标:通过多重酶联免疫吸附试验和定量聚合酶链反应测量 PRP 对滑液蛋白和 MSC 基因表达水平的影响。
结果:在 PRP 治疗后 10 天测量了滑液中的新型生物标志物,包括白细胞介素 (IL)-5、IL-6、IL-10 和肿瘤坏死因子-α 的水平。用 PRP 治疗的患者的 MSC 中观察到基因表达谱的改变,包括基质金属蛋白酶和炎症标志物 (IL-6、IL-8、CCL2、TNF-α)。A2M 蛋白酶在 PRP 治疗后显著增加 (P =.005)。WOMAC 评分从基线水平下降了长达 3 个月,并在 PRP 组中在 6 个月和 12 个月时仍保持较低水平。相比之下,接受生理盐水注射的患者的 WOMAC 评分在长达 12 个月的时间内相对不变。
结论:我们报告了生物标志物 A2M 的显著变化 (P =.005),以及细胞标志物表达的差异,并推测 PRP 通过改变炎症环境、基质降解和血管生成生长因子来调节局部膝关节滑膜环境。PRP 治疗组疼痛和僵硬程度较轻,功能评分提高。
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