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眼球震颤可能是脊髓小脑性共济失调 3 型早期阶段的首个神经学迹象。

Nystagmus may be the first neurological sign in early stages of spinocerebellar ataxia type 3.

机构信息

Universidade Federal de São Paulo, Departamento de Neurologia, Unidade de Ataxia, São Paulo SP, Brazil.

Universidade de Campinas, Departamento de Neurologia, Campinas SP, Brazil.

出版信息

Arq Neuropsiquiatr. 2021 Oct;79(10):891-894. doi: 10.1590/0004-282X-ANP-2020-0386.

Abstract

BACKGROUND

Spinocerebellar ataxia type 3 (SCA3) is the most common autosomal dominant spinocerebellar ataxia worldwide. Almost all patients with SCA3 exhibit nystagmus and/or saccades impairment.

OBJECTIVE

To investigate the presence of nystagmus as an early neurological manifestation, before ataxia, in some patients with SCA3 in the first six months of the disease.

METHODS

We evaluated a series of 155 patients with clinically and molecularly proven SCA3 between 2013 and 2020. Data regarding sex, age, age at onset, disease duration, CAG repeat expansion length, first symptom, presence of ataxia, scores on SARA and ICARS scales, and presence and characteristics of nystagmus were collected.

RESULTS

We identified seven patients with symptomatic SCA3 who presented with isolated nystagmus. In these seven individuals the age at onset ranged from 24 to 57 years, and disease duration from four to six months.

CONCLUSIONS

Our study showed that nystagmus may be the first neurological sign in SCA3. This clinical observation reinforces the idea that the neurodegenerative process in SCA3 patients may start in vestibular system connections or in flocculonodular lobe. This study adds relevant information about pre-symptomatic features in SCA3 that may work as basis for a better understanding of brain degeneration and for future therapeutic clinical trials.

摘要

背景

脊髓小脑性共济失调 3 型(SCA3)是全球最常见的常染色体显性遗传性脊髓小脑性共济失调。几乎所有 SCA3 患者均存在眼球震颤和/或扫视运动障碍。

目的

研究在疾病的前 6 个月内,一些 SCA3 患者在出现共济失调之前,眼球震颤是否作为早期神经系统表现存在。

方法

我们评估了 2013 年至 2020 年间临床和分子确诊的 155 例 SCA3 患者。收集的数据包括性别、年龄、发病年龄、病程、CAG 重复扩展长度、首发症状、是否存在共济失调、SARA 和 ICARS 评分、眼球震颤的存在和特征。

结果

我们发现了 7 例出现症状性 SCA3 的患者,他们仅表现为孤立性眼球震颤。这 7 例患者的发病年龄为 24-57 岁,病程为 4-6 个月。

结论

我们的研究表明,眼球震颤可能是 SCA3 的首发神经系统症状。这一临床观察结果进一步证实,SCA3 患者的神经退行性过程可能始于前庭系统连接或绒球小结叶。本研究增加了关于 SCA3 患者的症状前特征的重要信息,这可能为更好地了解大脑退化以及未来的治疗性临床试验提供依据。

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