School of Communication Sciences and Disorders, College of Health Professions and Sciences, Biionix Cluster, University of Central Florida, Orlando, FL, USA.
Department of Communication Sciences and Disorders, East Carolina University, Greenville, NC, USA.
Cleft Palate Craniofac J. 2023 Oct;60(10):1250-1259. doi: 10.1177/10556656221100674. Epub 2022 May 15.
Velopharyngeal dysfunction (VPD) associated with 22q11.2 deletion syndrome (22q11.2DS) has a complex etiology. This study had 3 aims: (1) assess differences in velopharyngeal and levator muscle configuration during rest versus sustained speech production (2) compare differences in velopharyngeal changes between children with and without 22q11.2DS (3) examine the relationship between adenoid thickness, pharyngeal depth, and velopharyngeal changes.
Cross-sectional.
A total of 22 participants, 11 with 22q11.2DS and 11 controls with normal speech and velopharyngeal anatomy (ages 4-12 years), underwent nonsedated MRI at rest and during sustained /i/. Differences in velar and levator muscle contraction across the 2 different conditions were analyzed, using matched paired -tests. Mean differences across participant groups were examined. Correlation analyses were also conducted.
When comparing differences between rest and sustained phoneme production (aim 1), significant ( < .05) differences were noted for all velar and levator muscle variables. For differences in velopharyngeal changes between children with and without 22q11.2DS (aim 2), VP ratio and effective VP ratio were noted to be significantly different. Pharyngeal depth and adenoid thickness were correlated with velar and levator muscle change measures and ratios (aim 3).
Results from this study provide quantitative in vivo measurements of the contracted levator muscle and velum in young children with 22q11.2DS. Results demonstrated that VP ratio and EVP ratio are significantly different between children with and without 22q11.2DS and that pharyngeal depth is a strong clinical determinant of VPD in children with 22q11.2DS.
与 22q11.2 缺失综合征(22q11.2DS)相关的咽腔功能障碍(VPD)具有复杂的病因。本研究有 3 个目的:(1)评估在休息和持续言语产生时,软腭和提腭肌的结构差异;(2)比较 22q11.2DS 儿童与无 22q11.2DS 儿童之间的咽腔变化差异;(3)研究腺样体厚度、咽腔深度与咽腔变化的关系。
横断面研究。
共 22 名参与者,11 名患有 22q11.2DS,11 名具有正常言语和咽腔解剖结构的对照者(年龄 4-12 岁),在非镇静状态下进行 MRI 检查,分别在休息和持续发/i/音时进行。采用配对样本 t 检验分析 2 种不同条件下软腭和提腭肌收缩的差异。比较了各组参与者之间的平均差异。还进行了相关性分析。
在比较休息和持续发音时的软腭和提腭肌差异(目的 1)时,所有软腭和提腭肌变量均有显著差异(<0.05)。在比较有无 22q11.2DS 儿童之间的咽腔变化差异(目的 2)时,VP 比值和有效 VP 比值有显著差异。咽腔深度和腺样体厚度与软腭和提腭肌变化的测量值和比值相关(目的 3)。
本研究结果为患有 22q11.2DS 的幼儿提供了活体收缩提腭肌和软腭的定量测量。结果表明,有无 22q11.2DS 儿童的 VP 比值和 EVP 比值有显著差异,并且咽腔深度是 22q11.2DS 儿童 VPD 的重要临床决定因素。