Pecori Alessandro, Luppieri Valentina, Santin Aurora, Spedicati Beatrice, Zampieri Stefania, Cadenaro Milena, Girotto Giorgia, Concas Maria Pina
Institute for Maternal and Child Health-IRCCS "Burlo Garofolo", Via dell'Istria 65, 34137 Trieste, Italy.
Department of Medicine, Surgery and Health Sciences, University of Trieste, Strada di Fiume, 447, 34149 Trieste, Italy.
Biomedicines. 2024 Jan 28;12(2):304. doi: 10.3390/biomedicines12020304.
Bruxism is a worldwide oral health problem. Although there is a consensus about its multifactorial nature, its precise etiopathogenetic mechanisms are unclear. This study, taking advantage of a deeply characterized cohort of 769 individuals (aged 6-89 years) coming from Northern Italy's genetically isolated populations, aims to epidemiologically describe environmental risk factors for bruxism development and identify genes potentially involved through a Genome-Wide Association Study (GWAS) approach. Logistic mixed models adjusted for age and sex were performed to evaluate associations between bruxism and possible risk factors, e.g., anxiety, smoking, and alcohol and caffeine intake. A case-control GWAS (135 cases, 523 controls), adjusted for age, sex, and anxiety, was conducted to identify new candidate genes. The GTEx data analysis was performed to evaluate the identified gene expression in human body tissues. Statistical analyses determined anxiety as a bruxism risk factor (OR = 2.54; 95% CI: 1.20-5.38; -value = 0.015), and GWAS highlighted three novel genes potentially associated with bruxism: (topSNP = rs2046718; -value = 2.63 × 10), (topSNP = rs571497947; -value = 4.68 × 10), and (topSNP = rs2324342; -value = 7.47 × 10). The GTEx data analysis showed their expression in brain tissues. Overall, this work provided a deeper understanding of bruxism etiopathogenesis with the long-term perspective of developing personalized therapeutic approaches for improving affected individuals' quality of life.
磨牙症是一个全球性的口腔健康问题。尽管人们对其多因素性质已达成共识,但其确切的病因发病机制尚不清楚。本研究利用来自意大利北部基因隔离人群的769名个体(年龄在6 - 89岁之间)这一特征深入的队列,旨在从流行病学角度描述磨牙症发生的环境风险因素,并通过全基因组关联研究(GWAS)方法识别可能涉及的基因。采用经年龄和性别调整的逻辑混合模型来评估磨牙症与可能的风险因素之间的关联,例如焦虑、吸烟、饮酒和咖啡因摄入。进行了一项经年龄、性别和焦虑调整的病例对照GWAS(135例病例,523例对照),以识别新的候选基因。进行GTEx数据分析以评估所识别基因在人体组织中的表达。统计分析确定焦虑是磨牙症的一个风险因素(OR = 2.54;95% CI:1.20 - 5.38;P值 = 0.015),GWAS突出了三个可能与磨牙症相关的新基因: (顶级单核苷酸多态性 = rs2046718;P值 = 2.63 × 10)、 (顶级单核苷酸多态性 = rs571497947;P值 = 4.68 × 10)和 (顶级单核苷酸多态性 = rs2324342;P值 = 7.47 × 10)。GTEx数据分析显示它们在脑组织中表达。总体而言,这项工作从长期角度为开发个性化治疗方法以改善受影响个体的生活质量,对磨牙症的病因发病机制提供了更深入的理解。