Rosales Alberto Sierra, Rodríguez Eduardo Alberto Villaseñor, González Christian Lorena López, Arellano Edy David Rubio, Rubio Susan Andrea Gutiérrez, Cobián Teresa Arcelia García
Departamento de Clínicas Odontológicas Integrales, Centro Universitario de Ciencias de la Salud, Universidad de Guadalajara.
Instituto de Terapéutica Experimental y Clínica, CUCS - Centro Universitario de Ciencias de la Salud; Universidad de Guadalajara.
Braz Dent J. 2020 Mar-Apr;31(2):152-156. doi: 10.1590/0103-6440202003037.
Anterior disc displacement with reduction (DDWR) is considered one of the most common disorders within the temporomandibular joint (TMJ), with a prevalence of 41% in adults. Matrix metalloproteinases play an important role in the degradation of the TMJ and the matrix metalloproteinase 1 (MMP1) 1607 1G/2G polymorphism increases the local expression of MMP1 thus leading to accelerated degradation of the extracellular matrix. The objective of this study was to evaluate the association between the 1607 1G/2G polymorphism of MMP1 gene and DDWR in a group of Mexican individuals from western Mexico. A total of 67 unrelated individuals, between the ages of 18 and 36 years, of both genders, were included in this study. Study participants with DDWR were required to meet the Research Diagnostic Criteria for Temporomandibular Disorders (RDC/TMD), while a second control group of 90 individuals without DDWR were also included. Both groups were required to have paternal and maternal ancestry (grandparents) of the same geographic and ethnic region. Genotypes were determined using the nested PCR technique. The 1G/2G polymorphism was found in 68.7%, followed by 2G/2G in 25.4% and 1G/1G in 6.0% of the cases group. While the prevalence in the control group was 55.5% for the 1G/2G polymorphism, 26.6% for 1G/1G and 17.7% for 2G/2G. An association was found between the 2G allele of the 1607 1G/2G polymorphism of MMP1 gene and the presence of DDWR in the patients of western Mexico.
可复性盘前移位(DDWR)被认为是颞下颌关节(TMJ)最常见的疾病之一,在成年人中的患病率为41%。基质金属蛋白酶在TMJ的降解中起重要作用,基质金属蛋白酶1(MMP1)1607 1G/2G多态性会增加MMP1的局部表达,从而导致细胞外基质加速降解。本研究的目的是评估墨西哥西部一组个体中MMP1基因1607 1G/2G多态性与DDWR之间的关联。本研究共纳入了67名年龄在18至36岁之间、男女不限的无亲缘关系个体。患有DDWR的研究参与者需符合颞下颌关节紊乱病研究诊断标准(RDC/TMD),同时还纳入了90名无DDWR的第二对照组个体。两组个体均要求其父母(祖父母)来自相同的地理和种族区域。使用巢式PCR技术确定基因型。病例组中1G/2G多态性的发生率为68.7%,其次2G/2G为25.4%,1G/1G为6.0%。而对照组中1G/2G多态性的患病率为55.5%,1G/1G为26.6%,2G/2G为17.7%。在墨西哥西部患者中,发现MMP1基因1607 1G/2G多态性的2G等位基因与DDWR的存在之间存在关联。