Shingu M, Obata K, Ezaki I, Tomari K, Fujikawa Y, Wada T, Nonaka S, Suenaga Y, Iwata K, Nobunaga M
Department of Clinical Immunology, Kyushu University, Beppu-city.
Ryumachi. 1995 Feb;35(1):15-24.
Stromelysin-1 (MMP-3) is a metalloproteinase that degrades articular cartilage matrix in patients with rheumatoid arthritis (RA). We measured MMP-3 in the sera from patients with RA and other connective tissue diseases using specific sandwich EIA and studied its clinical significance in early onset RA. MMP-3 level in healthy control (n = 170) was significantly higher in male than in female. The level of MMP-3 in RA was significantly and dramatically higher than in healthy control, osteoarthritis, systemic lupus erythematosus, progressive systemic sclerosis, primary sjogren's syndrome, mixed connective tissue disease, gouty arthritis and traumatic arthritis. Serum MMP-3 significantly correlated with serum BUN or serum creatinine levels in SLE patients but not in RA patients. In early onset RA, serum MMP-3 level was significantly elevated. Furthermore, when the relationship between the serum MMP-3 level and X-ray findings of the joints in RA was studied, it was found that MMP-3 level was elevated even in stage I or II and that there was no statistical differences between stage I or II and stage III or IV, suggesting that serum MMP-3 level is elevated in the early stage of initial inflammatory process when only mild cartilage degradation is seen. These results suggest that measurements of serum MMP-3 is an important tool for establishing diagnosis of early onset RA, and that serum MMP-3 level may be a marker of cartilage destruction and of estimating therapeutic efficacy in early onset RA.
基质溶解素-1(MMP-3)是一种金属蛋白酶,可降解类风湿关节炎(RA)患者的关节软骨基质。我们使用特异性夹心酶免疫测定法检测了RA患者和其他结缔组织疾病患者血清中的MMP-3,并研究了其在早发性RA中的临床意义。健康对照者(n = 170)中男性的MMP-3水平显著高于女性。RA患者的MMP-3水平显著且大幅高于健康对照者、骨关节炎、系统性红斑狼疮、进行性系统性硬化症、原发性干燥综合征、混合性结缔组织病、痛风性关节炎和创伤性关节炎患者。血清MMP-3与SLE患者的血清尿素氮或血清肌酐水平显著相关,但与RA患者无关。在早发性RA中,血清MMP-3水平显著升高。此外,当研究血清MMP-3水平与RA患者关节X线表现之间的关系时,发现即使在I期或II期MMP-3水平也会升高,且I期或II期与III期或IV期之间无统计学差异,这表明在仅见轻度软骨降解的初始炎症过程早期血清MMP-3水平就会升高。这些结果表明,检测血清MMP-3是诊断早发性RA的重要工具,血清MMP-3水平可能是软骨破坏的标志物以及评估早发性RA治疗效果的指标。