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一生中的磨牙症以及[具体基因名称1]、[具体基因名称2]和[具体基因名称3]中的变体

Bruxism Throughout the Lifespan and Variants in , and .

作者信息

Vieira Alexandre R, Scariot Rafaela, Gerber Jennifer T, Arid Juliana, Küchler Erika C, Sebastiani Aline M, Palinkas Marcelo, Díaz-Serrano Kranya V, Torres Carolina P, Regalo Simone C H, Nelson-Filho Paulo, Bussaneli Diego G, Deeley Kathleen, Modesto Adriana

机构信息

Department of Oral Biology, University of Pittsburgh School of Dental Medicine, 412 Salk Pavilion, 335 Sutherland Drive, Pittsburgh, PA 15261, USA.

Department of Pediatric Dentistry, University of Pittsburgh School of Dental Medicine, Pittsburgh, PA 15213, USA.

出版信息

J Pers Med. 2020 May 27;10(2):44. doi: 10.3390/jpm10020044.

Abstract

Bruxism is a masticatory muscle activity characterized by grinding of the teeth and clenching of the jaw that causes tooth wear and breakage, temporomandibular joint disorders, muscle pain, and headache. Bruxism occurs in both adults and children. Clinical characteristics and habits were evaluated in an adult sample. Moreover, we used DNA samples from 349 adults and 151 children to determine the presence of association with specific genes. Genomic DNA was obtained from saliva. The markers and (metalloproteinase 2 ()), and (metalloproteinase 9 ()), and (cathecol-o-methyltransferase ()) were genotyped. Data were submitted to statistical analysis with a significance level of 0.05. In adults, in univariate logistic regression, presence of caries, attrition, and use of alcohol were increased in bruxism individuals ( < 0.05). In addition, in adults, there was an association between bruxism and (, = 0.0001) and bruxism and (, = 0.003). In children, a borderline association was observed for (, = 0.08). When we performed multivariate logistic regression analyses in adults, the same clinical characteristics remained associated with bruxism, and orthodontic treatment was also associated, besides , in the AG genotype ( = 0.015, OR: 3.40 (1.27-9.07)). For the first time, we provide statistical evidence that these genes are associate with bruxism.

摘要

磨牙症是一种咀嚼肌活动,其特征为牙齿磨动和牙关紧闭,可导致牙齿磨损与折断、颞下颌关节紊乱、肌肉疼痛和头痛。磨牙症在成人和儿童中均有发生。我们在一个成人样本中评估了临床特征和习惯。此外,我们使用了来自349名成人和151名儿童的DNA样本,以确定与特定基因的关联情况。基因组DNA取自唾液。对基质金属蛋白酶2(MMP2)的标记rs243865和rs2070737、基质金属蛋白酶9(MMP9)的标记rs3918242和rs17576、儿茶酚-O-甲基转移酶(COMT)的标记rs4680进行了基因分型。数据提交至显著性水平为0.05的统计分析。在成人中,单因素逻辑回归显示,磨牙症患者的龋齿、磨耗情况及饮酒情况增加(P<0.05)。此外,在成人中,磨牙症与MMP2(P = 0.0001)以及磨牙症与MMP9(P = 0.003)之间存在关联。在儿童中,观察到COMT存在临界关联(P = 0.08)。当我们在成人中进行多因素逻辑回归分析时,相同的临床特征仍与磨牙症相关,并且除MMP9外,正畸治疗在AG基因型中也与之相关(P = 0.015,OR:3.40(1.27 - 9.07))。我们首次提供了这些基因与磨牙症相关的统计证据。

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