학술논문

Coenzyme Q10 and spinocerebellar ataxias
Document Type
article
Source
Movement Disorders. 30(2)
Subject
Complementary and Integrative Health
Prevention
Nutrition
Clinical Research
Brain Disorders
Aetiology
2.1 Biological and endogenous factors
Adult
Age of Onset
Aged
Disease Progression
Female
Humans
Huntington Disease
Male
Middle Aged
Severity of Illness Index
Spinocerebellar Ataxias
Surveys and Questionnaires
Treatment Outcome
Ubiquinone
coenzyme Q10
statins
spinocerebellar ataxias
neurodegeneration
Clinical Sciences
Human Movement and Sports Sciences
Neurosciences
Neurology & Neurosurgery
Language
Abstract
The aim of this study was to investigate the association between drug exposure and disease severity in SCA types 1, 2, 3 and 6. The Clinical Research Consortium for Spinocerebellar Ataxias (CRC-SCA) enrolled 319 participants with SCA1, 2, 3, and 6 from 12 medical centers in the United States and repeatedly measured clinical severity by the Scale for Assessment and Rating of Ataxia (SARA), the Unified Huntington's Disease Rating Scale part IV (UHDRS-IV), and the 9-item Patient Health Questionnaire during July 2009 to May 2012. We employed generalized estimating equations in regression models to study the longitudinal effects of coenzyme Q10 (CoQ10), statin, and vitamin E on clinical severity of ataxia after adjusting for age, sex, and pathological CAG repeat number. Cross-sectionally, exposure to CoQ10 was associated with lower SARA and higher UHDRS-IV scores in SCA1 and 3. No association was found between statins, vitamin E, and clinical outcome. Longitudinally, CoQ10, statins, and vitamin E did not change the rates of clinical deterioration indexed by SARA and UHDRS-IV scores within 2 years. CoQ10 is associated with better clinical outcome in SCA1 and 3. These drug exposures did not appear to influence clinical progression within 2 years. Further studies are warranted to confirm the association.