Department of Surgical Sciences, Specialization School of Orthodontics, Dental School, University of Torino, Via Nizza 230, 10126 Torino, Italy.
Department of Surgical Sciences, Specialization School of Orthodontics, Dental School, University of Torino, Via Nizza 230, 10126 Torino, Italy; Department of Surgical Sciences, Gnathology Unit, Dental School, University of Torino, Via Nizza 230, 10126 Torino, Italy.
Arch Oral Biol. 2017 Nov;83:25-32. doi: 10.1016/j.archoralbio.2017.07.002. Epub 2017 Jul 5.
The aim of this article was to systematically review the literature to assess the relationship between risk factors and sleep bruxism (SB) in adults (age ≥18 years).
A systematic search of the following databases was carried out: PubMed, Embase, Scopus, Cochrane Oral Health Group's Trial Register and Cochrane Register of Controlled Trials, Web of Science, LILACs and SciELO. Nine out of the 4583 initially identified articles were selected. This review was conducted according to the guidelines from the Cochrane Handbook for Systematic Reviews of Interventions, with reporting in agreement to the Preferred Reporting Items for Systematic Reviews and Meta-analyses guidelines.
Among the nine analyzed articles, associations between SB and gastro-esophageal reflux disease (GERD) (OR=6.6, CI=1.4-30.9) was found in one randomized clinical trial (RCT). Four cross-sectional studies suggested history of SB during childhood (OR=8.1 CI=5.4-12-2), age (OR=3.1, CI=2.3-4.1) and chronic migraine (OR=3.8, C.I=1.8-7.8) as determinant factors for the development of SB. In one case-control study, patients with genetic polymorphisms were more likely to present SB (OR=4.3, CI=1.6-11.3). Smoking (OR=2.8, CI=2.2-3.5) and alcohol intake (OR=1.9, CI=1.2-2.8) showed moderate association in two case-control studies.
History of SB during childhood, gastro-esophageal reflux disease and genetic polymorphisms seem to be important risk factors associated to SB in adults. Dry mouth on awakening seems to be a protective factor. Association does not infer with causality. Even if the evidence emerged from the considered studies was clinically relevant, further studies are requested to better understand the biological mechanisms behind the described associations.
本文旨在系统回顾文献,评估成年人(年龄≥18 岁)中风险因素与磨牙症(SB)之间的关系。
对以下数据库进行系统检索:PubMed、Embase、Scopus、Cochrane 口腔健康组试验登记处和 Cochrane 对照试验登记处、Web of Science、LILACs 和 SciELO。从最初确定的 4583 篇文章中选出了 9 篇。本综述按照 Cochrane 干预系统评价手册的指南进行,报告符合系统评价和荟萃分析指南的首选报告项目。
在分析的 9 篇文章中,一项随机临床试验(RCT)发现 SB 与胃食管反流病(GERD)之间存在关联(OR=6.6,CI=1.4-30.9)。四项横断面研究表明,儿童时期有 SB 病史(OR=8.1,CI=5.4-12-2)、年龄(OR=3.1,CI=2.3-4.1)和慢性偏头痛(OR=3.8,CI=1.8-7.8)是 SB 发展的决定因素。在一项病例对照研究中,具有遗传多态性的患者更有可能出现 SB(OR=4.3,CI=1.6-11.3)。两项病例对照研究表明,吸烟(OR=2.8,CI=2.2-3.5)和饮酒(OR=1.9,CI=1.2-2.8)呈中度关联。
儿童时期有 SB 病史、胃食管反流病和遗传多态性似乎是成年人 SB 的重要危险因素。晨起口干似乎是一个保护因素。关联并不意味着因果关系。即使考虑到研究的证据具有临床相关性,但仍需要进一步的研究来更好地理解所描述关联背后的生物学机制。