Distinct attentional and executive profiles in neurofibromatosis type 1: Is there difference with primary attention deficit-hyperactivity disorder?

IF 2.3 3区 医学 Q3 CLINICAL NEUROLOGY European Journal of Paediatric Neurology Pub Date : 2024-06-01 DOI:10.1016/j.ejpn.2024.05.016
Laura Routier , Laurent Querné , Cécile Fontaine , Patrick Berquin , Anne-Gaëlle Le Moing
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Abstract

Purpose

Attentional and executive dysfunctions are the most frequent cognitive disorders in neurofibromatosis type 1 (NF1), with a high prevalence of attention deficit-hyperactivity disorder (ADHD). We (i) compared attentional profiles between NF1 children with and without ADHD and children with primary ADHD criteria and (ii) investigated the possible relationship between attentional disorders and “unidentified bright objects” (UBOs) in NF1.

Methods

This retrospective study included 47 NF1 children, 25 with ADHD criteria (NF1+adhd group), matched for age, sex, and cognitive level with 47 children with primary ADHD (ADHD group). We collected computer task (sustained-attention, visuomotor-decision, inhibition, and cognitive-flexibility tasks) scores normalized for age and sex, and brain magnetic resonance imaging data.

Results

(i) Working memory was impaired in all groups. (ii) Omissions (p < 0.002) and response-time variability (p < 0.05) in sustained-attention and visuomotor-decision tasks and errors (p < 0.02) in the cognitive-flexibility task were lower for the NFI+adhd and ADHD groups than for the NF1-no-adhd group. (iii) The NF1+adhd group had slower response times (p ≤ 0.02) for inhibition and visuomotor-decision tasks than the other groups. (iv) We found no relevant association between cognitive performance and UBOs.

Conclusions

NF1 children with ADHD have an attentional and executive functions deficit profile similar to that of children with primary ADHD, but with a slower response-time, increasing learning difficulties. The atypical connectivity of fronto-striatal pathways, poorer dopamine homeostasis, and increased GABA inhibition observed in NF1 renders vulnerable the development of the widely distributed neural networks that support attentional, working-memory, and executive functions.

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神经纤维瘤病 1 型的注意和执行特征与原发性注意缺陷多动障碍有区别吗?
目的 注意力和执行功能障碍是1型神经纤维瘤病(NF1)最常见的认知障碍,其中注意力缺陷多动障碍(ADHD)的发病率很高。我们(i)比较了有多动症和无多动症的 NF1 儿童与有原发性多动症标准的儿童之间的注意力状况,(ii)调查了注意力障碍与 NF1 儿童 "不明亮物"(UBO)之间可能存在的关系。方法这项回顾性研究纳入了 47 名 NF1 儿童,其中 25 名有多动症标准(NF1+adhd 组),与 47 名有原发性多动症的儿童(ADHD 组)在年龄、性别和认知水平上相匹配。我们收集了计算机任务(持续注意力任务、视觉运动决策任务、抑制任务和认知灵活性任务)的得分(按年龄和性别归一化)以及脑磁共振成像数据。(ii) NFI+adhd 组和 ADHD 组在持续注意力和视觉运动决策任务中的遗漏(p < 0.002)和反应时间变异性(p < 0.05)以及认知灵活性任务中的错误(p < 0.02)均低于 NF1 无 adhd 组。(iii) 与其他组相比,NF1+adhd 组在抑制和视觉运动决策任务中的反应时间较慢(p ≤ 0.02)。(结论NF1多动症儿童的注意力和执行功能缺陷与原发性多动症儿童相似,但反应时间较慢,增加了学习困难。在 NF1 中观察到的前额纹状体通路的非典型连接、较差的多巴胺稳态和 GABA 抑制增加,使支持注意力、工作记忆和执行功能的广泛分布的神经网络的发展变得脆弱。
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来源期刊
CiteScore
6.30
自引率
3.20%
发文量
115
审稿时长
81 days
期刊介绍: The European Journal of Paediatric Neurology is the Official Journal of the European Paediatric Neurology Society, successor to the long-established European Federation of Child Neurology Societies. Under the guidance of a prestigious International editorial board, this multi-disciplinary journal publishes exciting clinical and experimental research in this rapidly expanding field. High quality papers written by leading experts encompass all the major diseases including epilepsy, movement disorders, neuromuscular disorders, neurodegenerative disorders and intellectual disability. Other exciting highlights include articles on brain imaging and neonatal neurology, and the publication of regularly updated tables relating to the main groups of disorders.
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