[THE HIDDEN VESTIBULAR FEATURES OF MACHADO JOSEPH DISEASE (SPINOCEREBELLAR ATAXIA 3)].

Harefuah Pub Date : 2023-08-01
Zohar Elyoseph, Dario Geisinger, Roy Zaltzman, Matti Mintz, Carlos R Gordon
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Abstract

Introduction: Machado-Joseph disease (MJD) is an inherited neurodegenerative disease with progressive cerebellar ataxia manifested through lack of coordination and balance. MJD patients also present significant Vestibulo-Ocular Reflex (VOR) deficit but their whole vestibular features have not been previously evaluated. We aimed to evaluate whether MJD patients have vestibular features fitting the diagnostic criteria of Bilateral Vestibulopathy established by the International Society for Neuro-otology.

Methods: Sixteen MJD patients and 21 healthy controls underwent a detailed clinical neuro-otological examination including a quantitative evaluation of the VOR gain using the video Head Impulse Test (vHIT). Vestibular-related symptoms were evaluated by the Dizziness Handicap Inventory (DHI), the Activities-specific Balance Confidence Scale (ABC), the Vertigo Visual Scale (VVS). In addition, anxiety that is frequently present in vestibular disorders, was evaluated by the Beck Anxiety Inventory (BAI).

Results: MJD patients had significantly reduced horizontal VOR gain with significantly higher scores in all vestibular-related symptoms questionnaires. These symptoms scores were like those reported in studies evaluating patients with bilateral peripheral vestibular loss.

Conclusions: Beyond the cerebellar deficits, MJD patients have vestibular signs and symptoms fitting the diagnostic criteria of Bilateral Vestibulopathy established by the International Society for Neuro-otology. These findings are of relevance not only for the diagnosis and evaluation of progressive cerebellar diseases but also for the possible beneficial effect of vestibular rehabilitation techniques on dizziness, balance and the emotional, physiological and functional aspects of MJD.

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[machado Joseph病(脊髓小脑性共济失调3)的隐蔽性前庭特征]。
简介:Machado-Joseph病(MJD)是一种遗传性神经退行性疾病,伴有进行性小脑共济失调,表现为缺乏协调性和平衡性。MJD患者也表现出明显的前庭-眼反射(VOR)缺陷,但他们的整个前庭功能尚未被评估。我们的目的是评估MJD患者是否具有符合国际神经耳科学会建立的双侧前庭病变诊断标准的前庭特征。方法:16例MJD患者和21例健康对照者进行了详细的临床神经-耳科检查,包括使用视频头部脉冲测试(vHIT)定量评估VOR增益。采用头晕障碍量表(DHI)、活动特异性平衡信心量表(ABC)、眩晕视觉量表(VVS)评估前庭相关症状。此外,通过贝克焦虑量表(BAI)评估前庭疾病中经常出现的焦虑。结果:MJD患者水平VOR增益显著降低,所有前庭相关症状问卷得分显著升高。这些症状评分与评估双侧前庭外周功能丧失患者的研究报告相似。结论:除了小脑缺陷,MJD患者的前庭体征和症状符合国际神经耳科学会建立的双侧前庭病变的诊断标准。这些发现不仅与进行性小脑疾病的诊断和评估有关,而且与前庭康复技术对MJD的头晕,平衡以及情绪,生理和功能方面的可能有益作用有关。
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