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Sleep disorders in spinocerebellar ataxia type 10
Author(s) -
London Ester,
Camargo Carlos H. F.,
Zanatta Alessandra,
Crippa Ana C.,
Raskin Salmo,
Munhoz Renato P.,
Ashizawa Tetsuo,
Teive Hélio A. G.
Publication year - 2018
Publication title -
journal of sleep research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.297
H-Index - 117
eISSN - 1365-2869
pISSN - 0962-1105
DOI - 10.1111/jsr.12688
Subject(s) - spinocerebellar ataxia , epworth sleepiness scale , ataxia , polysomnography , excessive daytime sleepiness , audiology , arousal , medicine , sleep disorder , psychology , physical therapy , insomnia , apnea , psychiatry , neuroscience
Summary As sleep disturbances have been reported in spinocerebellar ataxias (SCAs), including types SCA1, SCA2, SCA3, SCA6 and SCA13, identification and management of these disturbances can help minimise their impact on SCA patients' overall body functions and quality of life. To our knowledge, there are no studies that investigate sleep disturbances in SCA10. Therefore, the aim of this study was to assess sleep disturbances in patients with SCA10. Twenty‐three SCA10 patients and 23 healthy controls were recruited. Patients were evaluated in terms of their demographic and clinical data, including disease severity (Scale for the Assessment and Rating of Ataxia, SARA) and excessive daytime sleepiness (Epworth Sleepiness Scale, ESS), and underwent polysomnography. SCA10 patients had longer rapid eye movement (REM) sleep ( p  = .04) and more REM arousals than controls ( p < .0001). There was a correlation of REM sleep onset with the age of onset of symptoms ( r  = .459), and with disease duration ( r  = −.4305). There also was correlation between the respiratory disturbance index (RDI) and SARA ( r  = −.4013), and a strong indirect correlation between arousal index and age at onset of symptoms ( r  = −.5756). In conclusion, SCA10 patients had sleep abnormalities that included more REM arousals and higher RDI than controls. Our SCA10 patients had sleep disorders related to shorter disease duration and lower severity of ataxia, in a pattern similar to that of other neurodegenerative diseases.

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