Teng Y T, Sodek J, McCulloch C A
Faculty of Dentistry, University of Toronto, Canada.
J Periodontal Res. 1992 Sep;27(5):544-52. doi: 10.1111/j.1600-0765.1992.tb01830.x.
Collagenolytic enzymes released by neutrophils are associated with the destruction of periodontium in periodontal diseases. Measurement of these enzymes in gingival crevicular fluid (GCF) could be used to test for periodontal diseases and thereby simplify diagnosis. To test this hypothesis, gelatinase (MMP-9) was analyzed in GCF samples with a simple assay system. GCF was collected by a mouthrinse method from 10 patients with gingivitis (G); 10 well-treated and maintained periodontitis patients (TP) without detectable loss of attachment; and 9 patients with recurrent loss of periodontal attachment (greater than 2 mm) and/or abscess formation (RP). Clinical measurements including tooth mobility (MOB) and gingival attachment level (GAL) were made monthly for a maximum of 10 months. Active and latent forms of gelatinase were measured by a functional assay using gelatin substrate-gel enzymography and the activities were quantified by laser densitometry. Reproducibility analysis demonstrated that the assay (inter-gel, inter-assay, inter-scan) and diurnal variations were small compared to biological variation. The presence of active gelatinase was detected in 97.8% of TP samples, 86.4% of RP samples, but in only 11.4% of G samples. In addition, the mean active gelatinase activity was found to be significantly higher (p less than 0.001) in the RP (71,006 U) than the TP (43,814 U) groups, both of which were higher (p less than 0.001) than the G group (2824 U). During periods of attachment loss, samples from the RP group exhibited a 2-fold increase of mean active gelatinase activity (129,414 U).(ABSTRACT TRUNCATED AT 250 WORDS)
中性粒细胞释放的胶原酶与牙周疾病中牙周组织的破坏有关。检测龈沟液(GCF)中的这些酶可用于检测牙周疾病,从而简化诊断。为验证这一假设,采用简单的检测系统分析了GCF样本中的明胶酶(MMP-9)。通过漱口法从10例牙龈炎患者(G组)、10例治疗良好且病情稳定、无附着丧失的牙周炎患者(TP组)以及9例有牙周附着反复丧失(大于2mm)和/或脓肿形成的患者(RP组)中收集GCF。每月进行包括牙齿松动度(MOB)和牙龈附着水平(GAL)在内的临床测量,最长持续10个月。使用明胶底物凝胶酶谱法通过功能检测测量明胶酶的活性和潜伏形式,并通过激光密度测定法定量活性。重复性分析表明,与生物学变异相比,该检测方法(凝胶间、检测间、扫描间)和昼夜变化较小。在97.8%的TP组样本、86.4%的RP组样本中检测到活性明胶酶,但G组样本中仅11.4%检测到。此外,发现RP组(71,006 U)的平均活性明胶酶活性显著高于TP组(43,814 U)(p<0.001),两组均高于G组(2824 U)(p<0.001)。在附着丧失期间,RP组样本的平均活性明胶酶活性增加了2倍(129,414 U)。(摘要截短至250字)