儿童和青少年单基因神经发育障碍的适应性功能。

IF 3.7 2区 医学 Q1 CLINICAL NEUROLOGY Developmental Medicine and Child Neurology Pub Date : 2025-01-23 DOI:10.1111/dmcn.16227
Emma K. Baker, Miya St John, Ruth Braden, Lottie D. Morison, Elana J. Forbes, Fatma Lelik, Stephen J. C. Hearps, David J. Amor, Angela T. Morgan
{"title":"儿童和青少年单基因神经发育障碍的适应性功能。","authors":"Emma K. Baker,&nbsp;Miya St John,&nbsp;Ruth Braden,&nbsp;Lottie D. Morison,&nbsp;Elana J. Forbes,&nbsp;Fatma Lelik,&nbsp;Stephen J. C. Hearps,&nbsp;David J. Amor,&nbsp;Angela T. Morgan","doi":"10.1111/dmcn.16227","DOIUrl":null,"url":null,"abstract":"<div>\n \n \n <section>\n \n <h3> Aim</h3>\n \n <p>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.</p>\n </section>\n \n <section>\n \n <h3> Method</h3>\n \n <p>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 (<i>CDK13</i>, <i>DYRK1A</i>, <i>FOXP2</i>, <i>KAT6A</i>, <i>KANSL1</i>, <i>SETBP1</i>, <i>BRPF1</i>, and <i>DDX3X</i>). Parents and caregivers completed the Vineland Adaptive Behavior Scales, Third Edition to assess communication, daily living, socialization, and motor skills.</p>\n </section>\n \n <section>\n \n <h3> Results</h3>\n \n <p>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 <i>BRPF1</i> or <i>KANSL1</i> had better adaptive behaviour skills compared to children with variants in <i>CDK13</i>, <i>DDX3X</i>, <i>DYRK1A,</i> and <i>KAT6A</i>, 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.</p>\n </section>\n \n <section>\n \n <h3> Interpretation</h3>\n \n <p>Transdiagnostic approaches to understand adaptive behaviour in monogenic NDDs provide a better understanding of individual strengths and challenges, enabling more targeted support.</p>\n </section>\n </div>","PeriodicalId":50587,"journal":{"name":"Developmental Medicine and Child Neurology","volume":"67 7","pages":"953-962"},"PeriodicalIF":3.7000,"publicationDate":"2025-01-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1111/dmcn.16227","citationCount":"0","resultStr":"{\"title\":\"Adaptive functioning in children and young adults with monogenic neurodevelopmental disorders\",\"authors\":\"Emma K. Baker,&nbsp;Miya St John,&nbsp;Ruth Braden,&nbsp;Lottie D. Morison,&nbsp;Elana J. Forbes,&nbsp;Fatma Lelik,&nbsp;Stephen J. C. Hearps,&nbsp;David J. Amor,&nbsp;Angela T. Morgan\",\"doi\":\"10.1111/dmcn.16227\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div>\\n \\n \\n <section>\\n \\n <h3> Aim</h3>\\n \\n <p>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.</p>\\n </section>\\n \\n <section>\\n \\n <h3> Method</h3>\\n \\n <p>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 (<i>CDK13</i>, <i>DYRK1A</i>, <i>FOXP2</i>, <i>KAT6A</i>, <i>KANSL1</i>, <i>SETBP1</i>, <i>BRPF1</i>, and <i>DDX3X</i>). Parents and caregivers completed the Vineland Adaptive Behavior Scales, Third Edition to assess communication, daily living, socialization, and motor skills.</p>\\n </section>\\n \\n <section>\\n \\n <h3> Results</h3>\\n \\n <p>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 <i>BRPF1</i> or <i>KANSL1</i> had better adaptive behaviour skills compared to children with variants in <i>CDK13</i>, <i>DDX3X</i>, <i>DYRK1A,</i> and <i>KAT6A</i>, 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.</p>\\n </section>\\n \\n <section>\\n \\n <h3> Interpretation</h3>\\n \\n <p>Transdiagnostic approaches to understand adaptive behaviour in monogenic NDDs provide a better understanding of individual strengths and challenges, enabling more targeted support.</p>\\n </section>\\n </div>\",\"PeriodicalId\":50587,\"journal\":{\"name\":\"Developmental Medicine and Child Neurology\",\"volume\":\"67 7\",\"pages\":\"953-962\"},\"PeriodicalIF\":3.7000,\"publicationDate\":\"2025-01-23\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://onlinelibrary.wiley.com/doi/epdf/10.1111/dmcn.16227\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Developmental Medicine and Child Neurology\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://onlinelibrary.wiley.com/doi/10.1111/dmcn.16227\",\"RegionNum\":2,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CLINICAL NEUROLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Developmental Medicine and Child Neurology","FirstCategoryId":"3","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1111/dmcn.16227","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CLINICAL NEUROLOGY","Score":null,"Total":0}
引用次数: 0

摘要

目的:研究单基因神经发育障碍(ndd)儿童的适应性行为特征,以确定综合征特异性或跨诊断方法是否能更好地了解这些ndd的适应性行为表型。方法:本横断面研究纳入243例(48%为女性)个体的父母和照顾者(年龄范围= 1-25岁;平均= 8年10个月,SD = 5年8个月),遗传上证实的单基因ndd (CDK13、DYRK1A、FOXP2、KAT6A、KANSL1、SETBP1、BRPF1和DDX3X)。家长和照顾者完成了Vineland适应行为量表,第三版,以评估沟通,日常生活,社交和运动技能。结果:线性回归模型比较单基因ndd之间的平均适应行为,调整了智力残疾的存在,结果显示组间差异不大。与CDK13、DDX3X、DYRK1A和KAT6A基因变异的儿童相比,BRPF1或KANSL1基因变异的儿童具有更好的适应行为技能,尽管不同基因域的组间差异有所不同。一项潜在剖面分析为五剖面模型提供了令人信服的证据。这些配置文件是同质的,在每个配置文件中具有相似的跨子域分数的延迟。此外,除了少数例外,每个单基因NDD在每个剖面中都有表示。解释:理解单基因ndd适应性行为的跨诊断方法可以更好地了解个体优势和挑战,从而提供更有针对性的支持。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

摘要图片

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
Adaptive functioning in children and young adults with monogenic neurodevelopmental disorders

Aim

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.

Method

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.

Results

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.

Interpretation

Transdiagnostic approaches to understand adaptive behaviour in monogenic NDDs provide a better understanding of individual strengths and challenges, enabling more targeted support.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
CiteScore
7.80
自引率
13.20%
发文量
338
审稿时长
3-6 weeks
期刊介绍: Wiley-Blackwell is pleased to publish Developmental Medicine & Child Neurology (DMCN), a Mac Keith Press publication and official journal of the American Academy for Cerebral Palsy and Developmental Medicine (AACPDM) and the British Paediatric Neurology Association (BPNA). For over 50 years, DMCN has defined the field of paediatric neurology and neurodisability and is one of the world’s leading journals in the whole field of paediatrics. DMCN disseminates a range of information worldwide to improve the lives of disabled children and their families. The high quality of published articles is maintained by expert review, including independent statistical assessment, before acceptance.
期刊最新文献
Neonates born at term with periventricular haemorrhagic infarction: Risk factors and clinical presentation. Paralisia cerebral no Brasil: Um estudo multicêntrico, transversal, e descritivo. Epidemiologia da paralisia cerebral no Brasil pela perspectiva da Classificação Internacional de Funcionalidade, Incapacidade e Saúde. Environmental supportiveness, physical activity, and sedentary time in children with cerebral palsy. Biomechanical and functional outcomes of high-burden and low-burden multilevel surgery in young people with cerebral palsy.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1