谷歌浏览器插件
订阅小程序
在清言上使用

Motor Function and Physiology in Youth with Neurofibromatosis Type 1.

Pediatric neurology(2023)

引用 0|浏览19
暂无评分
摘要
Background: Neurofibromatosis type 1 (NF1) is a genetic neurocutaneous disorder commonly associated with motor and cognitive symptoms that greatly impact quality of life. Transcranial magnetic stimulation (TMS) can quantify motor cortex physiology, reflecting the basis for impaired motor function as well as, possibly, clues for mechanisms of effective treatment. We hypothesized that children with NF1 have impaired motor function and altered motor cortex physiology compared to typically developing (TD) control children and children with attention-deficit/hyperactivity disorder (ADHD).Methods: Children aged 8-17 years with NF1 (n = 21) were compared to children aged 8-12 years with ADHD (n = 59) and TD controls (n = 88). Motor development was assessed using the Physical and Neurological Examination for Subtle Signs (PANESS) scale. The balance of inhibition and excitation in motor cortex was assessed using the TMS measures short-interval cortical inhibition (SICI) and intra-cortical facilitation (ICF). Measures were compared by diagnosis and tested using bivariate correlations and regression for association with clinical characteristics.Results: In NF1, ADHD severity scores were intermediate between the ADHD and TD cohorts, but total PANESS scores were markedly elevated (worse) compared to both (P < 0.001). Motor cortex ICF (excit-atory) was significantly lower in NF1 than in TD and ADHD (P < 0.001), but SICI (inhibitory) did not differ. However, in NF1, better PANESS scores correlated with lower SICI ratios (more inhibition; r = 0.62, P = 0.003) and lower ICF ratios (less excitation; r = 0.38, P = 0.06). Conclusions: TMS-evoked SICI and ICF may reflect processes underlying abnormal motor function in children with NF1.(c) 2023 Elsevier Inc. All rights reserved.
更多
查看译文
关键词
Neurofibromatosis,Transcranial magnetic stimulation,Pediatric neurology,Motor development,Biomarker
AI 理解论文
溯源树
样例
生成溯源树,研究论文发展脉络
Chat Paper
正在生成论文摘要