Adaptive functioning in children and young adults with monogenic neurodevelopmental disorders

被引:0
|
作者
Baker, Emma K. [1 ,2 ,3 ]
St John, Miya [1 ,4 ]
Braden, Ruth [1 ,4 ]
Morison, Lottie D. [1 ,4 ]
Forbes, Elana J. [1 ]
Lelik, Fatma [1 ]
Hearps, Stephen J. C. [5 ,6 ]
Amor, David J. [2 ,7 ]
Morgan, Angela T. [1 ,4 ,8 ]
机构
[1] Murdoch Childrens Res Inst, Speech & Language, Parkville, Vic 3032, Australia
[2] Univ Melbourne, Dept Paediat, Melbourne, Vic, Australia
[3] La Trobe Univ, Sch Psychol & Publ Hlth, Melbourne, Vic, Australia
[4] Univ Melbourne, Dept Audiol & Speech Pathol, Melbourne, Vic, Australia
[5] Murdoch Childrens Res Inst, Brain & Mind, Parkville, Vic, Australia
[6] Univ Melbourne, Dept Crit Care, Melbourne, Vic, Australia
[7] Murdoch Childrens Res Inst, Neurodisabil & Rehabil, Parkville, Vic, Australia
[8] Royal Childrens Hosp, Speech Pathol Dept, Parkville, Vic, Australia
来源
DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY | 2025年
基金
英国医学研究理事会; 澳大利亚国家健康与医学研究理事会;
关键词
AUTISM;
D O I
10.1111/dmcn.16227
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
AimTo 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.MethodThis 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.ResultsLinear 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.InterpretationTransdiagnostic approaches to understand adaptive behaviour in monogenic NDDs provide a better understanding of individual strengths and challenges, enabling more targeted support.
引用
收藏
页数:10
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