遗传性神经发育障碍中的眩晕和头晕:一项国际横断面研究。

IF 4.8 2区 医学 Q1 CLINICAL NEUROLOGY
Christophe Lopez, Pauline Burger, Jean-Louis Mandel, Romain Coutelle
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引用次数: 0

摘要

背景:具有遗传基础的神经发育障碍(ndd)通常与神经和感觉障碍相关;然而,前庭症状仍未得到充分认识。眩晕、头晕和失衡可显著影响日常功能,但其在ndd患者中的患病率和遗传关联尚不清楚。本研究旨在评估遗传性ndd患者前庭症状的发生情况。方法:我们使用来自GenIDA数据库的数据进行了一项国际前瞻性横断面研究,其中包括确诊的遗传疾病,智力发育障碍和/或其他ndd的个体。护理人员完成了一项调查,评估眩晕、头晕、平衡问题、情绪困扰、精神合并症以及偏头痛和癫痫等相关疾病的发生情况。我们分析了过去12个月眩晕的患病率,并探讨了潜在的遗传因素。结果:在过去的12个月里,遗传性ndd患者的眩晕发生率(11.8%)和失衡发生率(27.7%)明显高于普通人群。然而,只有不到40%的患者接受了正式的眩晕诊断。值得注意的是,眩晕与感觉不快乐和抑郁的可能性增加显著相关。20个与ndd有因果关系的遗传异常被确定为眩晕的潜在诱因,包括22q11.2微缺失和ANKRD11、MED13L、PACS1和SHANK3的变异。讨论:眩晕在遗传性ndd患者中似乎非常普遍,但未得到充分诊断。发现的遗传异常表明:(1)眩晕可能是ndd的内在组成部分,反映了导致内耳畸形、前庭网络功能障碍、小脑异常和癫痫以及其他神经发育特征的共同遗传途径;和/或(2)早期前庭功能障碍可能加重神经发育障碍。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Vertigo and dizziness in genetic neurodevelopmental disorders: an international cross-sectional study.

Background: Neurodevelopmental disorders (NDDs) with a genetic basis are frequently associated with neurological and sensory impairments; yet vestibular symptoms remain underrecognized. Vertigo, dizziness, and imbalance can significantly impact daily functioning, but their prevalence and genetic associations in individuals with NDDs are poorly understood. This study aimed to assess the occurrence of vestibular symptoms in individuals with genetic NDDs.

Methods: We conducted an international, prospective cross-sectional study using data from the GenIDA database, which includes individuals with confirmed genetic disorders, intellectual developmental disorders and/or other NDDs. Caregivers completed a survey assessing the occurrence of vertigo, dizziness, and balance issues, as well as emotional distress, psychiatric comorbidities, and associated conditions such as migraine and epilepsy. We analyzed the prevalence of vertigo in the past 12 months and explored potential genetic contributors.

Results: The occurrence rate of vertigo (11.8%) and imbalance (27.7%) in the past 12 months was dramatically increased in individuals with genetic NDDs compared to that observed in the general population. However, less than 40% of patients had received a formal diagnosis for their vertigo. Notably, vertigo was significantly associated with an increased likelihood of feeling unhappy and depressed. Twenty genetic anomalies causally involved in NDDs were identified as potential contributors to vertigo, including 22q11.2 microdeletions and variants in ANKRD11, MED13L, PACS1 and SHANK3.

Discussion: Vertigo appears highly prevalent, yet underdiagnosed, in individuals with genetic NDDs. The identified genetic anomalies suggest that (1) vertigo may be an intrinsic component of NDDs, reflecting shared genetic pathways leading to inner ear malformations, vestibular network dysfunction, cerebellar abnormalities, and epilepsy, alongside other neurodevelopmental features; and/or (2) early vestibular dysfunction may exacerbate neurodevelopmental impairments.

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来源期刊
Journal of Neurology
Journal of Neurology 医学-临床神经学
CiteScore
10.00
自引率
5.00%
发文量
558
审稿时长
1 months
期刊介绍: The Journal of Neurology is an international peer-reviewed journal which provides a source for publishing original communications and reviews on clinical neurology covering the whole field. In addition, Letters to the Editors serve as a forum for clinical cases and the exchange of ideas which highlight important new findings. A section on Neurological progress serves to summarise the major findings in certain fields of neurology. Commentaries on new developments in clinical neuroscience, which may be commissioned or submitted, are published as editorials. Every neurologist interested in the current diagnosis and treatment of neurological disorders needs access to the information contained in this valuable journal.
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