Volume 28, Issue 3 pp. 955-964
ORIGINAL ARTICLE

Genetic profile and clinical characteristics of Chinese patients with spinocerebellar ataxia type 2: A multicenter experience over 10 years

Lu Yang

Lu Yang

Department of Neurology and Research Center of Neurology in Second Affiliated Hospital, and Key Laboratory of Medical Neurobiology of Zhejiang Province, Zhejiang University School of Medicine, Hangzhou, China

Contribution: Data curation (supporting), Formal analysis (lead), ​Investigation (lead), Methodology (lead), Project administration (lead), Visualization (lead), Writing - original draft (lead)

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Yi Dong

Yi Dong

Department of Neurology and Research Center of Neurology in Second Affiliated Hospital, and Key Laboratory of Medical Neurobiology of Zhejiang Province, Zhejiang University School of Medicine, Hangzhou, China

Department of Neurology, Huashan Hospital, Fudan University, Shanghai, China

Contribution: Conceptualization (equal), Data curation (supporting), Funding acquisition (supporting), Resources (lead), Writing - review & editing (supporting)

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Yin Ma

Yin Ma

Department of Neurology and Research Center of Neurology in Second Affiliated Hospital, and Key Laboratory of Medical Neurobiology of Zhejiang Province, Zhejiang University School of Medicine, Hangzhou, China

Contribution: ​Investigation (supporting), Methodology (supporting), Software (lead), Visualization (supporting)

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Wang Ni

Wang Ni

Department of Neurology and Research Center of Neurology in Second Affiliated Hospital, and Key Laboratory of Medical Neurobiology of Zhejiang Province, Zhejiang University School of Medicine, Hangzhou, China

Department of Neurology, First Affiliated Hospital, Fujian Medical University, Fuzhou, China

Contribution: Project administration (supporting), Software (supporting), Supervision (lead), Visualization (supporting)

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Zhi-Ying Wu

Corresponding Author

Zhi-Ying Wu

Department of Neurology and Research Center of Neurology in Second Affiliated Hospital, and Key Laboratory of Medical Neurobiology of Zhejiang Province, Zhejiang University School of Medicine, Hangzhou, China

CAS Center for Excellence in Brain Science and Intelligence Technology, Shanghai, China

Correspondence

Zhi-Ying Wu, Department of Neurology and Research Center of Neurology in Second Affiliated Hospital, and Key Laboratory of Medical Neurobiology of Zhejiang Province, Zhejiang University School of Medicine, 88 Jiefang Road, Hangzhou 310009, China.

Email: [email protected]

Contribution: Conceptualization (equal), Data curation (lead), Funding acquisition (lead), Writing - review & editing (lead)

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First published: 18 October 2020
Citations: 6

Abstract

Background and purpose

Spinocerebellar ataxia type 2 (SCA2) is the second most common type of spinocerebellar ataxia in China. However, data on the clinical and genetic features of Chinese SCA2 patients are scarce. This study aims to provide a comprehensive description of in the Chinese SCA2 cohort.

Methods

A total of 135 patients with SCA2 from 92 families and 104 unrelated normal controls were recruited from three medical centers between 2008 and 2020. Sanger sequencing and TA cloning were used to determine the CAG repeat length and intrinsic structure. The clinical data of patients with SCA2, including electromyography, magnetic resonance imaging, positron-emission tomography, and clinical scale scores, were recorded.

Results

The mean ± SD age at onset of SCA2 patients was 32.6 ± 11.9 years and the corresponding CAG repeat length was 42.1 ± 3.6. CAG repeat length accounted for 64% of the age-at-onset variance. We observed that patients had a significantly lower proportion of (CAG)8CAA(CAG)4CAA(CAG)8 within normal alleles than normal controls (48.8% vs. 64.9%; p = 0.003), while the distribution of the proportion of (CAG)13CAA (CAG)8 was the opposite. Peripheral neuropathy was frequent, occurring in 75.9% of the patients. Parkinsonism was relatively common, with a frequency of 11.8%. Two patients with parkinsonism had a significantly more severe reduction in dopamine transporter levels in the bilateral striatum than the one patient with pure ataxia. An infant-onset case of SCA2 with more than 180 CAG repeats was characterized by global development delay, hypotonia and hearing impairment.

Conclusions

This study describes the genetic profile and clinical characteristics of the largest SCA2 cohort to date in the Chinese population and analyzes inter-population differences. Many aspects of this study population were different from other populations with SCA2.

CONFLICT OF INTEREST

The authors declare no financial or other conflicts of interest.

DATA AVAILABILITY STATEMENT

The data that support the findings of this study are available from the corresponding author upon reasonable request.

AUTHOR CONTRIBUTIONS

L. Yang: DataCuration (supporting); FormalAnalysis (lead); Investigation (lead); Methodology (lead); ProjectAdministration (lead); Visualization (lead); WritingOriginalDraft (lead). Y. Dong: Conceptualization (equal); DataCuration (supporting); Fundingacquisition (supporting); Resources (lead); WritingReviewEditing (supporting). Y. Ma: Investigation (supporting); Methodology (supporting); Software (lead); Visualization (supporting). W. Ni: ProjectAdministration (supporting); Software (supporting); Supervision (lead); Visualization (supporting). Z.-Y. Wu: Conceptualization (equal); DataCuration (lead); Fundingacquisition (lead); WritingReviewEditing (lead).

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