Quantitative assessment of postural instability in spinocerebellar ataxia type 3 patients

Objective Spinocerebellar ataxia type 3 (SCA3) is one of the most common hereditary neurodegenerative diseases, with balance instability as main symptom. Balance quantification is crucial for evaluating the efficacy of therapeutic interventions. However, balance evaluation in SCA3 is often subject t...

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Veröffentlicht in:Annals of clinical and translational neurology 2020-08, Vol.7 (8), p.1360-1370
Hauptverfasser: Liu, Xia‐Hua, Li, Ying, Xu, Hao‐Ling, Sikandar, Arif, Lin, Wei‐Hong, Li, Gui‐He, Li, Xiao‐Fen, Alimu, Alimire, Yu, Sheng‐Bin, Ye, Xiang‐Hui, Wang, Ning, Ni, Jun, Chen, Wan‐Jin, Gan, Shi‐Rui
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Sprache:eng
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Zusammenfassung:Objective Spinocerebellar ataxia type 3 (SCA3) is one of the most common hereditary neurodegenerative diseases, with balance instability as main symptom. Balance quantification is crucial for evaluating the efficacy of therapeutic interventions. However, balance evaluation in SCA3 is often subject to bias. Here, we aimed to quantitatively evaluate postural instability and investigate the relationship between postural instability and clinical characteristics in SCA3 patients. Methods Sixty‐two SCA3 patients and 62 normal controls were recruited, and their postural balance was measured using a posturographic platform. Principal component analysis was performed as data reduction to identify postural instability factors. Multivariable linear regression was used to investigate potential risk factors for postural instability and to explore whether postural instability predicts the severity and progression of ataxia in SCA3 patients. Results We found SCA3 patients experience postural instability characterized by significant impairment in static and dynamic stability. The condition without visual feedback was the most sensitive measure in differentiating SCA3 from controls. Regression analyses revealed that ataxia severity predicted both static (P = 0.014) and dynamic stability (P = 0.001). Likewise, along with expanded CAG repeats (P 
ISSN:2328-9503
2328-9503
DOI:10.1002/acn3.51124