Aji Nur Rahman Ahmad Seno, Yucel-Lindberg Tülay, Räisänen Ismo T, Kuula Heidi, Nieminen Mikko T, Mc Crudden Maelíosa T C, Listyarifah Dyah, Lundmark Anna, Lundy Fionnuala T, Gupta Shipra, Sorsa Timo
Department of Oral and Maxillofacial Diseases, Head and Neck Center, University of Helsinki and Helsinki University Hospital, 00290 Helsinki, Finland.
Department of Periodontics, Faculty of Dentistry, Universitas Gadjah Mada, Jalan Denta No. 1 Sekip Utara, 10 Sleman, Yogyakarta 55281, Indonesia.
Diagnostics (Basel). 2024 May 15;14(10):1011. doi: 10.3390/diagnostics14101011.
This study investigated in vivo regulation and levels of active matrix metalloproteinase-8 (aMMP-8), a major collagenolytic protease, in periodontitis.
Twenty-seven adults with chronic periodontitis (CP) and 30 periodontally healthy controls (HC) were enrolled in immunohistochemistry and transcriptomics analytics in order to assess (Td) dentilisin and MMP-8 immunoexpression, mRNA expression of MMP-8 and its regulators (IL-1β, MMP-2, MMP-7, TIMP-1). Furthermore, the periodontal anti-infective treatment effect was monitored by four different MMP-8 assays (aMMP-8-IFMA, aMMP-8-Oralyzer, MMP-8-activity [RFU/minute], and total MMP-8 by ELISA) among 12 CP (compared to 25 HC).
Immunohistochemistry revealed significantly more -dentilisin and MMP-8 immunoreactivities in CP vs. HC. Transcriptomics revealed significantly elevated IL-1β and MMP-7 RNA expressions, and MMP-2 RNA was slightly reduced. No significant differences were recorded in the relatively low or barely detectable levels of MMP-8 mRNAs. Periodontal treatment significantly decreased all MMP-8 assay levels accompanied by the assessed clinical indices (periodontal probing depths, bleeding-on-probing, and visual plaque levels). However, active but not total MMP-8 levels persisted higher in CP than in periodontally healthy controls.
In periodontal health, there are low aMMP-8 levels. The presence of -dentilisin in CP gingivae is associated with elevated aMMP-8 levels, potentially contributing to a higher risk of active periodontal tissue collagenolysis and progression of periodontitis. This can be detected by aMMP-8-specific assays and online/real-time aMMP-8 chair-side testing.
本研究调查了牙周炎中主要的胶原溶解蛋白酶——活性基质金属蛋白酶8(aMMP-8)的体内调节及水平。
纳入27名慢性牙周炎(CP)成人患者和30名牙周健康对照者(HC)进行免疫组织化学和转录组学分析,以评估牙本质素(Td)和MMP-8免疫表达、MMP-8及其调节因子(IL-1β、MMP-2、MMP-7、TIMP-1)的mRNA表达。此外,在12名CP患者(与25名HC对照)中,通过四种不同的MMP-8检测方法(aMMP-8免疫荧光微球法、aMMP-8口腔分析仪、MMP-8活性[相对荧光单位/分钟]以及ELISA法检测总MMP-8)监测牙周抗感染治疗效果。
免疫组织化学显示,与HC相比,CP患者中牙本质素和MMP-8免疫反应性显著更高。转录组学显示,IL-1β和MMP-7的RNA表达显著升高,MMP-2的RNA略有降低。MMP-8 mRNA水平相对较低或几乎检测不到,未记录到显著差异。牙周治疗使所有MMP-8检测水平显著降低,同时伴有评估的临床指标(牙周探诊深度、探诊出血和可见菌斑水平)改善。然而,CP患者中活性MMP-8水平而非总MMP-8水平仍高于牙周健康对照者。
在牙周健康状态下,aMMP-8水平较低。CP牙龈中牙本质素的存在与aMMP-8水平升高有关,可能导致牙周组织胶原溶解活性增加和牙周炎进展风险更高。这可通过aMMP-8特异性检测以及在线/实时aMMP-8椅旁检测来发现。