Suppr超能文献

有先兆和无先兆偏头痛中的亚临床前庭小脑功能障碍。

Subclinical vestibulocerebellar dysfunction in migraine with and without aura.

作者信息

Harno H, Hirvonen T, Kaunisto M A, Aalto H, Levo H, Isotalo E, Kallela M, Kaprio J, Palotie A, Wessman M, Färkkilä M

机构信息

Department of Neurology, Helsinki University Central Hospital, Finland.

出版信息

Neurology. 2003 Dec 23;61(12):1748-52. doi: 10.1212/01.wnl.0000098882.82690.65.

Abstract

OBJECTIVE

In patients with migraine, neurotologic symptoms and signs occur commonly. The authors' aim was to determine whether neurotologic findings are in accordance with the type of migraine and whether test findings differ from those of healthy controls.

METHODS

The authors examined 36 patients with various types of migraine classified by International Headache Society criteria. Comprehensive neurotologic tests were performed between attacks: video-oculography (VOG), electronystagmography, static posturography, and audiometry on 12 patients with migraine with aura (MA) and 24 patients with migraine without aura (MO). Results were compared to those of test-specific nonmigrainous control groups. Only eight migraineurs (six with MA and two with MO) had vertigo or dizziness.

RESULTS

Despite the absence of clinical neurotologic symptoms, most of the patients with migraine (83%) showed abnormalities in at least one of these tests. Both migraine types differed significantly from the control group (in VOG, in saccadic accuracy, and in static posturography). Vestibular findings tended to be more severe in MA than in MO.

CONCLUSIONS

These data suggest that interictal neurotologic dysfunction in MA and MO share similar features and that the defective oculomotor function is mostly of vestibulocerebellar origin.

摘要

目的

偏头痛患者常出现神经耳科症状和体征。作者旨在确定神经耳科检查结果是否与偏头痛类型相符,以及检查结果与健康对照者是否不同。

方法

作者检查了36例根据国际头痛协会标准分类的不同类型偏头痛患者。在发作间期进行了全面的神经耳科检查:对12例有先兆偏头痛(MA)患者和24例无先兆偏头痛(MO)患者进行了视频眼震图(VOG)、眼震电图、静态姿势描记法和听力测定。将结果与特定检查的非偏头痛对照组进行比较。只有8例偏头痛患者(6例MA和2例MO)有眩晕或头晕症状。

结果

尽管没有临床神经耳科症状,但大多数偏头痛患者(83%)至少在其中一项检查中出现异常。两种类型的偏头痛与对照组相比均有显著差异(在VOG、扫视准确性和静态姿势描记法方面)。MA的前庭检查结果往往比MO更严重。

结论

这些数据表明,MA和MO的发作间期神经耳科功能障碍具有相似特征,且动眼功能缺陷主要源于前庭小脑。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验