Alvarenga María Olimpia Paz, Ferreira Railson de Oliveira, Magno Marcela Baraúna, Fagundes Nathalia Carolina Fernandes, Maia Lucianne Cople, Lima Rafael Rodrigues
Laboratory of Functional and Structural Biology, Institute of Biological Sciences, Federal University of Pará, Belém, Brazil.
Department of Pediatric Dentistry and Orthodontics, School of Dentistry, Federal University of Rio de Janeiro, Rio de Janeiro, Brazil.
Front Physiol. 2019 Jul 3;10:832. doi: 10.3389/fphys.2019.00832. eCollection 2019.
An amount of cognition decline is normal with aging; however, intrinsic and extrinsic risk factors may exacerbate it, affecting social and occupational tasks. Masticatory dysfunction (MD), as a general term, refers to an impairment in the masticatory function triggered by a structural factor, such as tooth loss; functional factors, such as weaker bite force or a poorer masticatory performance; or both factors. MD acting as a source of chronic stress, promotes functional and morphological changes on the hippocampus, a brain area crucial for learning and memory abilities. This study aimed to synthesize evidence on the association between MD and cognitive deficit (CD), and demonstrate whether might be adequately considered as a risk factor. Observational studies were screened in seven online databases; the search strategy (PECO) was focused in observational studies with humans as a population (P), presenting groups exposed (E), and non-exposed (C) to tooth loss, in which cognition parameters were measured and compared between groups (O). The final selection included only those studies comparing the effect in cognition between subjects having ≥20 remaining teeth and <20 remaining teeth, considering the latter as a structural factor triggering MD by the literature. Searching and data extraction were conducted following PRISMA guidelines. Qualitative and risk of bias evaluations were performed. The meta-analysis (MA) was constructed including the odds ratio (OR) and its 95% confidence interval (CI) comparing two groups-with/without MD. The level of evidence was rated by Grading Recommendations Assessment, Development and Evaluation (GRADE) approach. In total, 5,666 citations were identified, 14 accomplished our eligibility criteria, and nine were include in the MA. The MA demonstrates that individuals with MD had 46% higher chance to presented CD (OR 2.24 [1.73, 2.90], < 0.00001, = 46%). The level of evidence was rated as low by GRADE. Despite the low certainty in evidence, according to our MA, MD is positively associated with increased risk of CD. However, more studies including other factors underlying MD and similar measurements should be conducted to obtain a strong estimate of the risk.
随着年龄增长,一定程度的认知能力下降是正常的;然而,内在和外在风险因素可能会加剧这种情况,影响社交和职业任务。咀嚼功能障碍(MD)作为一个通用术语,指的是由结构因素(如牙齿缺失)、功能因素(如咬合力较弱或咀嚼性能较差)或两者共同引发的咀嚼功能损害。MD作为慢性应激源,会促使海马体发生功能和形态变化,海马体是对学习和记忆能力至关重要的脑区。本研究旨在综合关于MD与认知缺陷(CD)之间关联的证据,并证明MD是否可被充分视为一个风险因素。在七个在线数据库中筛选观察性研究;搜索策略(PECO)聚焦于以人类为研究对象(P)的观察性研究,这些研究呈现出暴露于牙齿缺失的组(E)和未暴露于牙齿缺失的组(C),在其中测量并比较两组之间的认知参数(O)。最终入选的仅为那些比较剩余牙齿≥20颗和<20颗的受试者在认知方面影响的研究,根据文献,将后者视为引发MD的结构因素。按照PRISMA指南进行搜索和数据提取。进行定性和偏倚风险评估。构建荟萃分析(MA),包括比较有/无MD两组的优势比(OR)及其95%置信区间(CI)。证据水平采用推荐分级评估、制定与评价(GRADE)方法进行评级。总共识别出5666条引文,14项符合我们的纳入标准,9项纳入荟萃分析。荟萃分析表明,患有MD的个体出现CD的几率高46%(OR 2.24 [1.73, 2.90],P<0.00001,I² = 46%)。证据水平经GRADE评定为低。尽管证据的确定性较低,但根据我们的荟萃分析,MD与CD风险增加呈正相关。然而,需要开展更多纳入MD潜在其他因素及类似测量的研究,以获得对该风险的有力估计。