Sleep Disorders in Spinocerebellar Ataxia Type 2 Patients

• Published in: Neuro-degenerative diseases Vol. 8; no. 6; pp. 447 - 454
• Main Authors: Velázquez-Pérez, Luis, Voss, Ursula, Rodríguez-Labrada, Roberto, Auburger, Georg, Canales Ochoa, Nalia, Sánchez Cruz, Gilberto, Galicia Polo, Lourdes, Haro Valencia, Reyes, Aguilera Rodríguez, Raúl, Medrano Montero, Jacqueline, Laffita Mesa, Jose M., Tuin, Inka
• Format: Journal Article
• Language: English
• Published: Basel, Switzerland S. Karger AG 01.01.2011
• Subjects: Adolescent; Adult; Biomarkers; DNA - genetics; Electromyography; Female; Humans; Male; Middle Aged; Neurologic Examination; Original Paper; Phenotype; Polysomnography; Reverse Transcriptase Polymerase Chain Reaction; Sleep Wake Disorders - etiology; Sleep, REM - physiology; Spinocerebellar Ataxias - complications; Spinocerebellar Ataxias - genetics; Trinucleotide Repeat Expansion; Young Adult; Biomarkers; Sleep disorders; Periodic leg movements; REM sleep, without atonia; Spinocerebellar ataxia
• ISSN: 1660-2854; 1660-2862
• DOI: 10.1159/000324374

Background: Sleep disturbances are common features in spinocerebellar ataxias (SCAs). Nevertheless, sleep data on SCA2 come from scarce studies including few patients, limiting the evaluation of the prevalence and determinants of sleep disorders. Objective: To assess the frequency and possible determinants of sleep disorders in the large and homogeneous SCA2 Cuban population. Methods: Thirty-two SCA2 patients and their age- and sex-matched controls were studied by video-polysomnography and sleep interviews. Results: The most striking video-polysomnography features were rapid eye movement (REM) sleep pathology and periodic leg movements (PLMs). REM sleep abnormalities included a consistent reduction of the REM sleep percentage and REM density as well as an increase in REM sleep without atonia (RWA). REM sleep and REM density decreases were closely related to the increase in ataxia scores, whereas the RWA percentage was influenced by the cytosine-adenine-guanine (CAG) repeats. PLMs were observed in 37.5% of cases. The PLM index showed a significant association with the ataxia score and disease duration but not with CAG repeats. Conclusions: REM sleep pathology and PLMs are closely related to SCA2 severity, suggesting their usefulness as disease progression markers. The RWA percentage is influenced by the CAG repeats and might thus be a sensitive parameter for reflecting polyglutamine toxicity. Finally, as PLMs are sensible to drug treatment, they represents a new therapeutic target for the symptomatic treatment of SCA2.