前交叉韧带重建后软骨代谢和基质重塑的系统性生物标志物:一项前瞻性研究

Lachlan M. Batty, Minh Huynh, Kate E. Webster, Natasha Vassileff, Jereme Spiers, Haydn J. Klemm, Brian M. Devitt, Timothy S. Whitehead, Andrew F. Hill, Julian A. Feller
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引用次数: 0

摘要

背景:前交叉韧带(ACL)损伤和重建与软骨内稳态改变和创伤后骨关节炎有关。软骨代谢的生物标志物可能在定量评价这一现象中起作用。目的:描述前交叉韧带重建后第一年软骨代谢和细胞外基质重塑的3种全身生物标志物的变化,并确定基线和术后12个月时间点生物标志物浓度的相关因素。研究设计:实验室对照研究。方法:通过一项纵向研究,在初次ACL重建前和术后6个月和12个月采集尿液和血清样本。共666例患者提供样本(平均±SD年龄,24.9±7.2岁,60.5%男性)。采用免疫测定法测定尿c -末端2型胶原交联末端肽(CTX-II)的浓度,CTX-II是2型胶原降解的标志;血清ⅱ型胶原n -前肽(PIIANP)是2型胶原合成的标志;血清基质金属蛋白酶3 (MMP-3),细胞外基质重塑的中介。采用线性混合建模和线性回归对数据进行分析。结果:尿CTX-II浓度从基线到6个月分别下降了25% (95% CI, 19%-31%)和37% (95% CI, 22%-42%),从基线到12个月(P < 0.001)。血清PIIANP从基线到6个月增加了40% (95% CI, 34%-47%) (P < 0.001), 6至12个月无显著变化。从基线到6个月和从基线到12个月,血清MMP-3分别增加35% (95% CI, 29%-42%)和44% (95% CI, 37%-52%) (P < .001)。在基线时间点,年龄、体重指数(BMI)、性别和从受伤到手术的时间是与生物标志物浓度相关的因素。在12个月的时间点,年龄、性别、BMI和从受伤到手术的时间与生物标志物浓度相关。结论:尿CTX-II浓度降低与血清PIIANP浓度升高可能提示在ACL重建后的前12个月内存在修复性软骨反应。血清MMP-3浓度的增加表明在同一时期持续和进行性细胞外基质重塑。主要不可改变的人口统计学因素与3种生物标志物的基线和12个月浓度相关。临床相关性:软骨代谢的生物标志物可能在ACL损伤患者的治疗中具有未来预后或决策作用。这可能包括预测创伤后关节炎。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Systemic Biomarkers of Chondral Metabolism and Matrix Remodeling After Anterior Cruciate Ligament Reconstruction: A Prospective Study
Background: Anterior cruciate ligament (ACL) injuries and reconstruction are associated with alterations in chondral homeostasis and posttraumatic osteoarthritis. Biomarkers of chondral metabolism may have a role in quantitatively evaluating this phenomenon. Purposes: To describe changes in 3 systemic biomarkers of chondral metabolism and extracellular matrix remodeling during the first year after ACL reconstruction and to identify factors associated with biomarker concentrations at the baseline and 12-month postoperative timepoints. Study Design: Controlled laboratory study. Methods: From a longitudinal study, urine and serum samples were taken immediately before primary ACL reconstruction and at 6 and 12 months postoperatively. A total of 666 patients provided samples (mean ± SD age, 24.9 ± 7.2 years; 60.5% male). Immunoassays were used to measure concentrations of urinary C-terminal cross-linked telopeptide of type 2 collagen (CTX-II), a marker of type 2 collagen degradation; serum N-propeptide of collagen IIA (PIIANP), a marker of type 2 collagen synthesis; and serum matrix metalloproteinase 3 (MMP-3), a mediator of extracellular matrix remodeling. Linear mixed modeling and linear regression were used for data analysis. Results: Urinary CTX-II concentrations decreased by 25% (95% CI, 19%-31%) from baseline to 6 months and by 37% (95% CI, 22%-42%) from baseline to 12 months, respectively ( P < .001). Serum PIIANP increased by 40% (95% CI, 34%-47%) from baseline to 6 months ( P < .001) with no significant change between 6 and 12 months. Serum MMP-3 increased by 35% (95% CI, 29%-42%) and 44% (95% CI, 37%-52%) from baseline to 6 months and from baseline to 12 months respectively ( P < .001). At the baseline timepoint, age, body mass index (BMI), sex, and time from injury to surgery were factors associated with biomarker concentrations. At the 12-month timepoint, age, sex, BMI, and time from injury to surgery were associated with biomarker concentrations. Conclusion: Decreasing urinary CTX-II concentrations coupled with increasing serum PIIANP concentrations may suggest a reparative chondral response within the first 12 months after ACL reconstruction. Increasing serum MMP-3 concentrations suggested persistent and progressive extracellular matrix remodeling during this same period. Predominantly nonmodifiable demographic factors were associated with baseline and 12-month concentrations of the 3 biomarkers. Clinical Relevance: Biomarkers of chondral metabolism may have future prognostic or decision-making roles in the management of patients with ACL injury. This could include predicting posttraumatic arthritis.
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