Department of Orthodontics, Faculty of Medicine, University of Murcia, Murcia, Spain.
Department of Integral Pediatric Dentistry, Hospital Morales Meseguer, University of Murcia, 2ª Planta, C/Marqués de los Vélez s/n, 30008, Murcia, Murcia, Spain.
Sci Rep. 2020 Nov 16;10(1):19895. doi: 10.1038/s41598-020-76984-5.
The aim of this study was to evaluate the craniofacial cephalometric characteristics of individuals with Down syndrome (DS), comparing them with healthy subjects. An electronic search was made in Pubmed, Embase, Lilacs, Scopus, Medline and Web of Science without imposing limitations on publication date or language. Studies were selecting following the Preferred Reporting Items for Systematic Reviews and Meta-analyses (PRISMA) statement. The PECO acronym was applied as follows: P (population), individuals with DS; E, (exposition) diagnosis of DS; C (comparison), individuals without DS; O (outcomes) craniofacial characteristics based on cephalometric measurements. Independent reviewers performed data extraction and assessed the methodological quality of the articles using the Newcastle-Ottawa Quality-Assessment-scale. Seven case-control studies were included in meta-analysis. Given the variability of the cephalometric measurements used, only those that had been reported in at least three or more works could be included. Anterior cranial base length (SN), posterior cranial base length (SBa), total cranial base length (BaN), effective length of the maxilla (CoA), sagittal relationship between subspinale and supramentale (ANB), anterior facial height (NMe), and posterior facial height (SGo) values were significantly lower in the DS population than among control subjects. No significant differences were found in sagittal position of subspinale relative to cranial base (SNA) and sagittal position of supramentale relative to cranial base (SNB). Summarizing, individuals with DS present a shorter and flatter cranial base than the general population, an upper jaw of reduced sagittal dimension, as well as a tendency toward prognatic profile, with the medium third of the face flattened and a reduced anterior and posterior facial heights.
本研究旨在评估唐氏综合征(Down syndrome,DS)患者的颅面头影测量特征,并与健康个体进行比较。在 Pubmed、Embase、Lilacs、Scopus、Medline 和 Web of Science 中进行了电子检索,未对发表日期或语言施加限制。研究按照系统评价和荟萃分析的首选报告项目(PRISMA)声明进行选择。PECO 缩写如下:P(人群),DS 患者;E(暴露),DS 诊断;C(比较),无 DS 个体;O(结局),基于头影测量的颅面特征。独立审查员使用 Newcastle-Ottawa 质量评估量表提取数据并评估文章的方法学质量。有 7 项病例对照研究被纳入荟萃分析。由于所使用的头影测量值存在变异性,只有至少有 3 项或更多研究报告的测量值才能被纳入。颅前底长度(SN)、颅后底长度(SBa)、总颅底长度(BaN)、上颌有效长度(CoA)、subspinale 与 supramentale 之间的矢状关系(ANB)、前面部高度(NMe)和后面部高度(SGo)在 DS 人群中明显低于对照组。subspinale 相对于颅底的矢状位置(SNA)和 supramentale 相对于颅底的矢状位置(SNB)在两组之间无显著差异。总之,DS 患者的颅底比一般人群更短、更平坦,上颌矢状维度减小,呈现出前突倾向,面部中三分之一变平,前后面高减小。