适度
神经纤维瘤病
共病
干预(咨询)
医学
心理学
临床心理学
联想(心理学)
发展心理学
纵向研究
幼儿
精神科
注意力缺陷
遗传(遗传算法)
纵向数据
生活质量研究
注意缺陷多动障碍
精神共病
年轻人
作者
Dan Liu,Pamela L. Wolters,Bonnie Klein-Tasman,Karin S. Walsh,Jonathan M. Payne,Natalie A. Pride,Stephanie M. Morris,Yang Hou
出处
期刊:Cancers
[Multidisciplinary Digital Publishing Institute]
日期:2026-02-06
卷期号:18 (3): 529-529
标识
DOI:10.3390/cancers18030529
摘要
Objective: The current study tested (1) how ADHD symptoms and internalizing or externalizing problems covaried across ages 3–18 in children with neurofibromatosis type 1 (NF1), and (2) whether demographic and NF1-specific factors moderated the associations. Method: We analyzed integrated cross-sectional data of 685 observations from 455 children and adolescents with NF1 (Mage = 9.79 years, SD = 3.88; 43% female) across six institutions in the United States and Australia. ADHD symptoms (inattention and hyperactivity/impulsivity) and internalizing/externalizing problems were assessed via parent-report measures. Time-varying effect modeling was employed to examine the age-specific associations between ADHD symptoms and internalizing/externalizing problems. Moderation analyses tested effects of sex, parental education, and NF1 inheritance mode (familial vs. sporadic). Results: Inattention and hyperactivity/impulsivity symptoms were associated with greater internalizing and externalizing problems across ages 3–17. Inattention links were similar across ages, while the hyperactivity/impulsivity-externalizing link was stronger in early childhood than during adolescence. NF1 inheritance mode significantly moderated the inattention-externalizing link, with stronger associations observed among children with familial NF1. Other moderators were nonsignificant. Conclusions: ADHD symptoms are robustly linked to internalizing and externalizing problems from childhood to middle adolescence in children with NF1, with familial NF1 emerging as a potentially elevated risk factor. Future longitudinal and experimental research is needed to inform integrated intervention approaches, especially for those with familial NF1.
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