[Treatment for Spinocerebellar Degeneration].


Journal

Brain and nerve = Shinkei kenkyu no shinpo
ISSN: 1881-6096
Titre abrégé: Brain Nerve
Pays: Japan
ID NLM: 101299709

Informations de publication

Date de publication:
May 2023
Historique:
medline: 18 5 2023
pubmed: 17 5 2023
entrez: 17 5 2023
Statut: ppublish

Résumé

No disease-modifying therapy has been established for spinocerebellar degeneration and multiple system atrophy, and only symptomatic therapy is currently available. Taltirelin and protirelin are drugs covered by health insurance for cerebellar ataxia symptoms, and are expected to suppress the progression of symptoms. Muscle relaxants are used for spasticity associated with spinocerebellar degeneration, and vasopressors and therapeutic agents for dysuria are used for autonomic symptoms of multiple system atrophy. It is necessary to develop a new therapeutic agent with a different mechanism of action, aimed specifically at modifying the disease progression in patients with spinocerebellar degeneration and multiple system atrophy.

Identifiants

pubmed: 37194519
pii: 1416202366
doi: 10.11477/mf.1416202366
doi:

Types de publication

English Abstract Journal Article

Langues

jpn

Sous-ensembles de citation

IM

Pagination

498-502

Auteurs

Masaaki Matsushima (M)

Department of Neurology, Faculty of Medicine and Graduate School of Medicine, Hokkaido University.

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Classifications MeSH