Arreguin-Cano Juan Antonio, Ayerdi-Nájera Brenda, Tacuba-Saavedra Arvey, Navarro-Tito Napoleón, Dávalos-Martínez Alfonso, Emigdio-Vargas Abel, Barrera-Rodríguez Elia, Blanco-García Nubia, Gutiérrez-Venegas Gloria, Ventura-Molina Elías, León-Dorantes Gladys
Unit of Clinical and Epidemiological Innovation of the State of Guerrero, Secretary of Health of the State of Guerrero, Av. Juan R. Escudero No. 158 Col. C.D. Renacimiento, 39715 Acapulco, Guerrero Mexico.
Laboratory of Cellular Biology of Cancer, School of Chemical Sciences-Biological, University Autonomy of Guerrero, Chilpancingo, Guerrero Mexico.
Diabetol Metab Syndr. 2019 Dec 30;11:113. doi: 10.1186/s13098-019-0510-2. eCollection 2019.
Type 2 diabetes mellitus (T2DM) and periodontitis are chronic inflammatory diseases with a bidirectional relationship. The uncontrolled levels of glucose in T2DM patients change the pathophysiology and balance of inflammatory mediators. Matrix Metalloproteinase-2 (MMP-2) is a zinc-dependent endopeptidase that is responsible for tissue remodeling and degradation of the extracellular matrix in periodontal tissue. Therefore, the uncontrolled levels of glucose in T2DM could lead to an imbalance in MMP-2 activity in saliva, favoring the development of periodontitis.
Ninety-seven T2DM patients from Hospital Dr. Donato Alarcon were included in the study. Following clinical examination, the patients were classified into four groups according to the presence and degree of periodontal disease and glycemic control. Blood and whole saliva samples (WSS) were collected from each patient. Blood samples were used for Hba1c and polymorphonuclear cells count determination, while WSS were used to determine MMP-2 activity, TIMP-1 and nitrite. MMP-2 activity was determined by zymography. TIMP-1 were determined by Western blotting, and nitric oxide (NO) levels were determined by the Griess method.
Of the 97 patients with T2DM, 66 had periodontitis of different severities: 18 patients had mild periodontitis, 15 had moderate and 33 had severe. Salivary MMP-2 activity, HbA1c and TIMP-1 were positively correlated with the severity of periodontitis. On the other hand, the increase in HbA1c was negatively correlated with MMP-2 activity and quantity of TIMP-1 but was positively correlated with nitrite levels.
T2DM with glycemic uncontrol conditions, distinct clinical alterations in periodontal tissue were identified, including a decrease in the gingival redness, increased the clinical attachment loss and imbalance of MMP-2/TIMP-1, as the possible causes of disorders promoting the progression of periodontitis. Accelerated periodontitis development with poor glycemic uncontrol likely results from the altered response of host defenses and decreased activity of polymorphonuclear cells. Taken together, these findings identify MMP-2 as a promising molecular market for periodontitis.
2型糖尿病(T2DM)和牙周炎是具有双向关系的慢性炎症性疾病。T2DM患者血糖水平失控会改变病理生理学以及炎症介质的平衡。基质金属蛋白酶-2(MMP-2)是一种锌依赖性内肽酶,负责牙周组织的组织重塑和细胞外基质降解。因此,T2DM患者血糖水平失控可能导致唾液中MMP-2活性失衡,从而促进牙周炎的发展。
纳入了来自多纳托·阿拉尔孔医生医院的97例T2DM患者。经过临床检查后,根据牙周疾病的存在情况和严重程度以及血糖控制情况将患者分为四组。采集每位患者的血液和全唾液样本(WSS)。血液样本用于测定糖化血红蛋白(Hba1c)和多形核细胞计数,而WSS用于测定MMP-2活性、组织金属蛋白酶抑制剂-1(TIMP-1)和亚硝酸盐。MMP-2活性通过酶谱法测定。TIMP-1通过蛋白质印迹法测定,一氧化氮(NO)水平通过格里斯方法测定。
在97例T2DM患者中,66例患有不同严重程度的牙周炎:18例患有轻度牙周炎,15例患有中度牙周炎,33例患有重度牙周炎。唾液MMP-2活性、糖化血红蛋白(HbA1c)和TIMP-1与牙周炎的严重程度呈正相关。另一方面,HbA1c的升高与MMP-2活性和TIMP-1的量呈负相关,但与亚硝酸盐水平呈正相关。
在血糖控制不佳的T2DM患者中,发现牙周组织存在明显的临床改变,包括牙龈红肿减轻、临床附着丧失增加以及MMP-2/TIMP-1失衡,这些可能是促进牙周炎进展的紊乱的原因。血糖控制不佳导致牙周炎加速发展可能是由于宿主防御反应改变和多形核细胞活性降低。综上所述,这些发现表明MMP-2是牙周炎一个有前景的分子指标。