Teles Flavia R F, Chandrasekaran Ganesh, Martin Lynn, Patel Michele, Kallan Michael J, Furquim Camila, Hamza Tahir, Cucchiara Andrew J, Kantarci Alpdogan, Urquhart Olivia, Sugai James, Giannobile William V
Department of Basic and Translational Sciences, School of Dental Medicine, University of Pennsylvania, Philadelphia, Pennsylvania, USA.
Center for Innovation and Precision Dentistry (CiPD), University of Pennsylvania, Philadelphia, Pennsylvania, USA.
J Clin Periodontol. 2024 Dec;51(12):1619-1631. doi: 10.1111/jcpe.14048. Epub 2024 Aug 5.
To identify serum- and salivary-derived inflammatory biomarkers of periodontitis progression and determine their response to non-surgical treatment.
Periodontally healthy (H; n = 113) and periodontitis patients (P; n = 302) were monitored bi-monthly for 1 year without therapy. Periodontitis patients were re-examined 6 months after non-surgical periodontal therapy (NSPT). Participants were classified according to disease progression: P0 (no sites progressed; P1: 1-2 sites progressed; P2: 3 or more sites progressed). Ten salivary and five serum biomarkers were measured using Luminex. Log-transformed levels were compared over time according to baseline diagnosis, progression trajectory and after NSPT. Significant differences were sought using linear mixed models.
P2 presented higher levels (p < .05) of salivary IFNγ, IL-6, VEGF, IL-1β, MMP-8, IL-10 and OPG over time. Serum analytes were not associated with progression. NSPT led to clinical improvement and significant reduction of IFNγ, IL-6, IL-8, IL-1β, MMP-8, IL-10, OPG and MMP-9 in saliva and of CRP, MMP-8, MMP-9 and MPO in serum.
Periodontitis progression results from a sustained pro-inflammatory milieu that is reflected in salivary biomarkers, but less so in serum, likely because of the limited amount of progression per patient. NSPT can significantly decrease the levels of several salivary analytes.
识别牙周炎进展过程中血清和唾液来源的炎症生物标志物,并确定它们对非手术治疗的反应。
对牙周健康者(H组;n = 113)和牙周炎患者(P组;n = 302)进行为期1年的每两个月一次的监测,期间不进行治疗。牙周炎患者在接受非手术牙周治疗(NSPT)6个月后再次接受检查。参与者根据疾病进展情况进行分类:P0(无部位进展);P1(1 - 2个部位进展);P2(3个或更多部位进展)。使用Luminex检测10种唾液和5种血清生物标志物。根据基线诊断、进展轨迹以及NSPT后情况,对经对数转换后的水平随时间进行比较。使用线性混合模型寻找显著差异。
随着时间推移,P2组唾液中IFNγ、IL - 6、VEGF、IL - 1β、MMP - 8、IL - 10和OPG水平较高(p < 0.05)。血清分析物与疾病进展无关。NSPT使临床症状改善,唾液中IFNγ、IL - 6、IL - 8、IL - 1β、MMP - 8、IL - 10、OPG和MMP - 9以及血清中CRP、MMP - 8、MMP - 9和MPO显著降低。
牙周炎进展源于持续的促炎环境,这在唾液生物标志物中有所体现,但在血清中体现较少,可能是因为每位患者的进展程度有限。NSPT可显著降低多种唾液分析物的水平。