P Popat Ravi, Bhavsar Neeta V, Popat Parita R
Govt. Dental College & Hospital, Civil Hospital Campus, Asarwa, Ahmedabad, Gujarat, India.
Govt. Dental College & Hospital, Civil Hospital Campus, Asarwa, Ahmedabad, Gujarat, India.
Singapore Dent J. 2014 Dec;35:59-64. doi: 10.1016/j.sdj.2014.07.003.
Matrix Metalloproteinases (MMPs) are directly responsible for pathogenesis of periodontal diseases and their activity is regulated by Tissue Inhibitor of Metalloproteinases (TIMPs). This study was aimed to evaluate changes in gingival crevicular fluid (GCF) levels of MMP-1 and TIMP-1 in periodontal health and disease.
Clinical parameters were recorded and GCF samples were collected from 30 subjects with chronic generalised periodontitis and 20 periodontally healthy subjects. Subjects with periodontitis underwent scaling and root planing (SRP). GCF samples were collected and clinical parameters were recorded again after 1 month of SRP. GCF levels of MMP-1 and TIMP-1 were detected by ELISA.
GCF levels of MMP-1 were significantly increased in subjects with periodontitis at baseline (P0) as compared to periodontally healthy subjects (C). GCF levels of MMP-1 reduced significantly in subjects with periodontitis after treatment (P1) as compared to P0. GCF levels of TIMP-1 were significantly reduced in P0 as compared to C. GCF levels of TIMP-1 increased significantly in P1 as compared to P0.
Substantial elevation in GCF levels of MMP-1 and reduction in TIMP-1 were found in periodontitis as compared to healthy subjects. GCF levels of MMP-1 and TIMP-1 improved significantly after treatment.
基质金属蛋白酶(MMPs)直接导致牙周疾病的发病机制,其活性受金属蛋白酶组织抑制剂(TIMPs)调节。本研究旨在评估牙周健康和疾病状态下龈沟液(GCF)中MMP - 1和TIMP - 1水平的变化。
记录临床参数,并从30名慢性广泛性牙周炎患者和20名牙周健康受试者中收集GCF样本。牙周炎患者接受龈上洁治和根面平整(SRP)治疗。在SRP治疗1个月后再次收集GCF样本并记录临床参数。通过酶联免疫吸附测定(ELISA)检测GCF中MMP - 1和TIMP - 1的水平。
与牙周健康受试者(C组)相比,牙周炎患者基线时(P0)GCF中MMP - 1水平显著升高。与P0相比,牙周炎患者治疗后(P1)GCF中MMP - 1水平显著降低。与C组相比,P0中TIMP - 1的GCF水平显著降低。与P0相比,P1中TIMP - 1的GCF水平显著升高。
与健康受试者相比,牙周炎患者GCF中MMP - 1水平大幅升高,TIMP - 1水平降低。治疗后,GCF中MMP - 1和TIMP - 1水平显著改善。