Baker Emma K, St John Miya, Braden Ruth, Morison Lottie D, Forbes Elana J, Lelik Fatma, Hearps Stephen J C, Amor David J, Morgan Angela T
Speech and Language, Murdoch Children's Research Institute, Parkville, Victoria, Australia.
Department of Paediatrics, University of Melbourne, Melbourne, Victoria, Australia.
Dev Med Child Neurol. 2025 Jul;67(7):953-962. doi: 10.1111/dmcn.16227. Epub 2025 Jan 23.
To examine the adaptive behaviour profiles of children with monogenic neurodevelopmental disorders (NDDs) to determine whether syndrome-specific or transdiagnostic approaches provide a better understanding of the adaptive behavioural phenotypes of these NDDs.
This cross-sectional study included parents and caregivers of 243 (48% female) individuals (age range = 1-25 years; mean = 8 years 10 months, SD = 5 years 8 months) with genetically confirmed monogenic NDDs (CDK13, DYRK1A, FOXP2, KAT6A, KANSL1, SETBP1, BRPF1, and DDX3X). Parents and caregivers completed the Vineland Adaptive Behavior Scales, Third Edition to assess communication, daily living, socialization, and motor skills.
Linear regression models comparing mean adaptive behaviours between monogenic NDDs, adjusting for the presence of intellectual disability, revealed few group differences. Children with variants in BRPF1 or KANSL1 had better adaptive behaviour skills compared to children with variants in CDK13, DDX3X, DYRK1A, and KAT6A, although group differences varied across domains. A latent profile analysis showed compelling evidence for a five-profile model. These profiles were homogeneous, with similar delays across the subdomain scores in each profile. Additionally, each monogenic NDD was represented in each profile, with a few exceptions.
Transdiagnostic approaches to understand adaptive behaviour in monogenic NDDs provide a better understanding of individual strengths and challenges, enabling more targeted support.
研究单基因神经发育障碍(NDDs)儿童的适应性行为特征,以确定综合征特异性方法或跨诊断方法是否能更好地理解这些NDDs的适应性行为表型。
这项横断面研究纳入了243名(48%为女性)经基因确诊的单基因NDDs(CDK13、DYRK1A、FOXP2、KAT6A、KANSL1、SETBP1、BRPF1和DDX3X)患者的父母和照料者(年龄范围=1至25岁;平均=8岁10个月,标准差=5岁8个月)。父母和照料者完成了《文兰适应性行为量表》第三版,以评估沟通、日常生活、社交和运动技能。
在对智力残疾的存在进行调整后,比较单基因NDDs之间平均适应性行为的线性回归模型显示,组间差异很少。与携带CDK13、DDX3X、DYRK1A和KAT6A变异的儿童相比,携带BRPF1或KANSL1变异的儿童具有更好的适应性行为技能,尽管各领域的组间差异有所不同。潜在剖面分析为一个五剖面模型提供了有力证据。这些剖面是同质的,每个剖面中的子领域得分都有类似的延迟。此外,每个单基因NDD在每个剖面中都有体现,只有少数例外。
采用跨诊断方法来理解单基因NDDs中的适应性行为,能更好地了解个体的优势和挑战,从而提供更有针对性的支持。