Escuela Superior de Odontología, Universidad Autónoma de Guerrero, Acapulco Guerrero, Mexico.
Escuela Superior de Ciencias Agropecuarias, Universidad Autónoma de Guerrero, Iguala Guerrero, Mexico.
Odontology. 2020 Jan;108(1):25-33. doi: 10.1007/s10266-019-00435-5. Epub 2019 Jun 18.
Periodontitis is modulated by a complex dysbiotic microbiota, these species stimulate upward the production of pro-inflammatory cytokines such as TNF-α, which, in turn, upregulates the production of bone resorption molecules. Enzymes such as MMP-8 and 9 have been associated with the destructive disease. This study evaluated the composition of periodontal microbiota with the checkerboard hybridization technique and its correlation with TNF-α, MMP-8, and MMP-9 evaluated with ELISA, of 80 patients (45 healthy, and 35 with chronic periodontitis). The frequency of the 18 species evaluated was higher in patients with bone loss compared with control group. TNF-α in gingival crevicular fluid was significantly higher in bone loss group (p < 0.01); MMP-8 (p = 0.34) by MMP-9 (p < 0.05) in bone loss group obtained lower values than in control group. Positive correlation of TNF-α was obtained with Aggregatibacter actinomycetemcomitans (rho = 0.38; p < 0.01), Fusobacterium nucleatum (rho = 0.25; p < 0.05) and Porphyromonas gingivalis (rho = 0.26; p < 0.05); negative correlation of MMP-8 with A. actinomycetemcomitans (rho = 0.26; p < 0.01), Capnocytophaga sputigena (rho = 0.33; p < 0.01), and F. nucleatum (rho = 0.21; p < 0.05); also negative correlation of MMP-9 with F. nucleatum (rho = 0.23; p < 0.05), P. gingivalis (rho = 0.23; p < 0.05), and Tannerella forsythia (rho = 0.26; p < 0.01). TNF-α increased due to the increase in each count of A. actinomycetemcomitans (β = 0.57; p = 0.00). The presence of A. actinomycetemcomitans (β = 1.88; p = 0.00), Campylobacter rectus (β = 0.78; p = 0.01), F. nucleatum (β = 0.65; p = 0.04), and P. gingivalis (β = 0.65; p = 0.04) significantly increases TNF-α levels. TNF-α in gingival crevicular fluid, despite the minimal amounts collected, is a good biomarker of periodontal disease; since levels of TNF-α increases with the increase of the most harmful species to the periodontium.
牙周炎受复杂的失调微生物群调节,这些物种会刺激促炎细胞因子如 TNF-α 的产生增加,而 TNF-α 反过来又会上调骨吸收分子的产生。MMP-8 和 9 等酶与破坏性疾病有关。本研究使用棋盘杂交技术评估牙周微生物群的组成,并使用 ELISA 评估其与 TNF-α、MMP-8 和 MMP-9 的相关性,共评估了 80 名患者(45 名健康者和 35 名慢性牙周炎患者)。与对照组相比,骨质流失患者中评估的 18 种物种的频率更高。骨损失组龈沟液中的 TNF-α 明显升高(p < 0.01);MMP-8(p = 0.34)和 MMP-9(p < 0.05)在骨损失组中获得的数值低于对照组。TNF-α与伴放线放线杆菌(rho = 0.38;p < 0.01)、核梭杆菌(rho = 0.25;p < 0.05)和牙龈卟啉单胞菌(rho = 0.26;p < 0.05)呈正相关;MMP-8 与伴放线放线杆菌(rho = 0.26;p < 0.01)、二氧化碳嗜纤维菌(rho = 0.33;p < 0.01)和核梭杆菌(rho = 0.21;p < 0.05)呈负相关;MMP-9 与核梭杆菌(rho = 0.23;p < 0.05)、牙龈卟啉单胞菌(rho = 0.23;p < 0.05)和福赛斯坦纳菌(rho = 0.26;p < 0.01)呈负相关。由于伴放线放线杆菌(β = 0.57;p = 0.00)计数的增加,TNF-α 增加。伴放线放线杆菌(β = 1.88;p = 0.00)、直肠弯曲杆菌(β = 0.78;p = 0.01)、核梭杆菌(β = 0.65;p = 0.04)和牙龈卟啉单胞菌(β = 0.65;p = 0.04)的存在显著增加 TNF-α 水平。尽管收集的龈沟液量很少,但龈沟液中的 TNF-α 是牙周病的良好生物标志物;因为 TNF-α 水平随着对牙周组织最有害的物种的增加而增加。