成人1型神经纤维瘤病的神经认知功能——一项全国性的基于人群的研究

IF 3.6 2区 医学 Q2 GENETICS & HEREDITY Orphanet Journal of Rare Diseases Pub Date : 2024-11-28 DOI:10.1186/s13023-024-03454-w
Karoline Doser, Jens Richardt Møllegaard Jepsen, Line Kenborg, Kamilla Woznica Miskowiak, Vanna Albieri, Susanne Oksbjerg Dalton, Anja Krøyer, Hanne Hove, John R Østergaard, Christoffer Johansen, Sven Asger Sørensen, John Mulvihill, Jeanette Falck Winther, Pernille Envold Bidstrup
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摘要

背景:1型神经纤维瘤病(NF1)是一种以各种躯体表现和认知障碍为特征的遗传病,但后者在成人中很少被描述。本研究旨在通过神经心理学测试和自我报告问卷来描述潜在的神经认知功能障碍。方法:在一项全国性的基于人群的研究中,包括103名患有NF1的成年人和38名年龄和性别匹配的NF1无对照者,我们使用综合神经认知测试来评估智力和视觉短期记忆、即时视觉空间回忆、反应时间、持续注意力、运动速度、计划、计划时间、工作记忆以及多任务处理,并使用问卷来评估执行功能。采用描述性统计、多变量方差分析(MANOVA)和具有重复测量方差分析(ANOVA)的一般线性模型。结果:我们观察到基于整体表现的认知功能有统计学上的显著差异。患有NF1的成年人在智力、视觉短期记忆、即时视觉空间回忆和持续注意力方面表现出显著的、中度至重度的损伤(p结论:这是第一个以人群为基础的NF1患者样本的研究,结果显示智力和其他认知功能受损。显著认知障碍和非显著认知功能差异的模式表明,NF1的认知特征是选择性的,而不是普遍性的认知缺陷。
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Neurocognitive functioning in adults with neurofibromatosis type 1- a nationwide population-based study.

Background: Neurofibromatosis type 1 (NF1) is a genetic condition characterized by various somatic manifestations and cognitive impairments, but the latter are sparsely described in adults. This study aimed at characterizing potential impairments of neurocognitive functions using neuropsychological tests as well as a self-report questionnaire.

Methods: In a nationwide, population-based study including 103 adults with NF1 and 38 age- and gender-matched NF1-free comparisons, we used a comprehensive neurocognitive test battery to assess intelligence and visual short-term memory, immediate visuospatial recall, reaction time, sustained attention, motor speed, planning, planning time, working memory as well as multitasking and a questionnaire to assess executive functions. Descriptive statistics, multivariate analysis of variance (MANOVA), and general linear models with repeated measure analysis of variance (ANOVA) were used.

Results: We observed a statistically significant difference in overall performance-based cognitive functioning. Adults with NF1 showed significant, moderate-to-severe impairments in intelligence, visual short-term memory, immediate visuospatial recall, sustained attention (p < 0.0001-0.002), and some executive functions (p = 0.008 - 0.001), whereas other cognitive functions (multitasking, reaction time, motor speed, spatial working memory, planning time, and planning efficacy as well as some self-reported executive functions) were unimpaired.

Conclusions: This is the first study with a population-based sample of persons with NF1 and the results show impairments of intelligence and other cognitive functions. The pattern of both significant cognitive impairments and non-significantly different cognitive functions suggests a cognitive profile of selective rather than generalized cognitive deficits in NF1.

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来源期刊
Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases 医学-医学:研究与实验
CiteScore
6.30
自引率
8.10%
发文量
418
审稿时长
4-8 weeks
期刊介绍: Orphanet Journal of Rare Diseases is an open access, peer-reviewed journal that encompasses all aspects of rare diseases and orphan drugs. The journal publishes high-quality reviews on specific rare diseases. In addition, the journal may consider articles on clinical trial outcome reports, either positive or negative, and articles on public health issues in the field of rare diseases and orphan drugs. The journal does not accept case reports.
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