| Literature DB >> 30363880 |
Santiago Perez-Lloret1,2, Olivier Flabeau3, Pierre-Olivier Fernagut4,5, Anne Pavy-Le Traon6,7, María Verónica Rey1,2, Alexandra Foubert-Samier4,5,8, Francois Tison4,5,8, Olivier Rascol6,7, Wassilios G Meissner4,5,8.
Abstract
MSA is a progressive neurodegenerative disorder characterized by autonomic failure and a variable combination of poor levodopa-responsive parkinsonism and cerebellar ataxia (CA). Current therapeutic management is based on symptomatic treatment. Almost one third of MSA patients may benefit from l-dopa for the symptomatic treatment of parkinsonism, whereas physiotherapy remains the best therapeutic option for CA. Only midodrine and droxidopa were found to be efficient for neurogenic hypotension in double-blind, controlled studies, whereas other symptoms of autonomic failure may be managed with off-label treatments. To date, no curative treatment is available for MSA. Recent results of neuroprotective and -restorative trials have provided some hope for future advances. Considerations for future clinical trials are also discussed in this review.Entities:
Keywords: ataxia; atypical parkinsonism; autonomic dysfunction; multiple system atrophy; treatment
Year: 2015 PMID: 30363880 PMCID: PMC6183186 DOI: 10.1002/mdc3.12145
Source DB: PubMed Journal: Mov Disord Clin Pract ISSN: 2330-1619