Poorsattar Bejeh-Mir Arash, Parsian Hadi, Akbari Khoram Maryam, Ghasemi Nafiseh, Bijani Ali, Khosravi-Samani Mahmoud
Dental Materials Research Center, Dentistry School, Babol University of Medical Sciences, Babol, Iran.
Social Determinants of Health Research Center, Babol University of Medical Sciences, Babol, Iran ; Biochemistry and Biophysics Department, Babol University of Medical Sciences, Babol, Iran.
Int J Mol Cell Med. 2014 Summer;3(3):138-45.
Diagnosis of subclinical and early stage clinical periodontal dysfunction could prevent from further socioeconomic burden. The aim of this study was to assess the diagnostic applicability of nitric oxide and its end-metabolites in periodontal tissue health and disease. Forty-two patients were enrolled and divided into three groups according to gingivitis (GI) and clinical attachment level (CAL) indices: a healthy group (GI<1, CAL<1), b: gingivitis (GI>1, CAL>1) and c: periodontitis (CAL>1) with 14 patients in each group. Unstimulated saliva and gingival crevicular fluid (GCF) were collected. Samples were evaluated for nitrite, nitrate and total nitric oxide contents with the ELISA method. In addition, CAL, GI, plaque index (PI), decay, missing, filling (DMFT) and bleeding index (BI) scores were also recorded. Except for GCF nitrite content (P= 0.89), there was an increasing trend for measured biomarkers in both saliva and GCF (Periodontitis> gingivitis> healthy periodontium, P< 0.05). Data remained stable after simultaneous adjustment for DMFT and BI scores as confounding factors. Sensitivity, specificity, positive predictive value, negative predictive value, cut point and p- value were as the followings: GCF nitrate (0.71, 0.11, 0.29,0.43, 4.97, P= 0.04), nitric oxide GCF ( 0.64, 0.18, 0.28, 0.5, 10.12, P= 0.04), nitrite saliva (0.93, 0.96,0.93,0.96,123.48, P< 0.001), salivary nitrate (0.93, 0.96, 0.93, 0.96, 123.6, P< 0.001), salivary nitric oxide (0.93, 0.96, 0.93, 0.96, 246.65, P <0.001). Our results revealed that NO plays an important role in the process of destruction of periodontal tissues. Within the limitation of our study, detecting NO biomarker and its end metabolites in saliva is of more value to assess the periodontal health comparing to GCF.
亚临床和早期临床牙周功能障碍的诊断可以避免进一步的社会经济负担。本研究的目的是评估一氧化氮及其终末代谢产物在牙周组织健康和疾病中的诊断适用性。纳入42例患者,根据牙龈炎(GI)和临床附着水平(CAL)指数分为三组:健康组(GI<1,CAL<1),b:牙龈炎组(GI>1,CAL>1)和c:牙周炎组(CAL>1),每组14例。收集非刺激性唾液和龈沟液(GCF)。采用ELISA法检测样本中的亚硝酸盐、硝酸盐和总一氧化氮含量。此外,还记录了CAL、GI、菌斑指数(PI)、龋失补(DMFT)和出血指数(BI)评分。除GCF亚硝酸盐含量外(P = 0.89),唾液和GCF中检测到的生物标志物均呈上升趋势(牙周炎>牙龈炎>健康牙周组织,P<0.05)。将DMFT和BI评分作为混杂因素进行同时调整后,数据保持稳定。敏感性、特异性、阳性预测值、阴性预测值、切点和p值如下:GCF硝酸盐(0.71,0.11,0.29,0.43,4.97,P = 0.04),GCF一氧化氮(0.64,0.18,0.28,0.5,10.12,P = 0.04),唾液亚硝酸盐(0.93,0.96,0.93,0.96,123.48,P<0.001),唾液硝酸盐(0.93,0.96,0.93,0.96,123.6,P<0.001),唾液一氧化氮(0.93,0.96,0.93,0.96,246.65,P<0.001)。我们的结果表明,NO在牙周组织破坏过程中起重要作用。在我们研究的局限性内,与GCF相比,检测唾液中的NO生物标志物及其终末代谢产物对评估牙周健康更有价值。