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The pathogenesis of multiple system atrophy: past, present, and future.
- Source :
-
Movement disorders : official journal of the Movement Disorder Society [Mov Disord] 2000 Sep; Vol. 15 (5), pp. 784-8. - Publication Year :
- 2000
-
Abstract
- Multiple system atrophy is a sporadic, adult-onset neurodegenerative disease of unknown etiology. The condition may be unique among neurodegenerative diseases by the prominent, if not primary, role played by the oligodendroglial cell in the pathogenetic process. Recent developments in our understanding of multiple system atrophy have included the detection of glial cytoplasmic inclusions and alpha-synuclein accumulation in these inclusions. The latter finding links multiple system atrophy as an "alpha-synucleinopathy" to Parkinson's disease and dementia with Lewy bodies. This article reviews recent important findings of potential relevance to the pathogenesis of multiple system atrophy. We also speculate on areas in which further advances may be made to progress our understanding of this devastating condition.
- Subjects :
- Biomarkers
Brain metabolism
Gene Expression Regulation
Genes, Regulator
Humans
Inclusion Bodies pathology
Multiple System Atrophy classification
Multiple System Atrophy genetics
Multiple System Atrophy metabolism
Multiple System Atrophy pathology
Nerve Tissue Proteins metabolism
Neuregulins genetics
Oligodendroglia metabolism
Polymorphism, Genetic
Synucleins
alpha-Synuclein
tau Proteins metabolism
Brain pathology
Inclusion Bodies metabolism
Multiple System Atrophy etiology
Mutation
Nerve Tissue Proteins genetics
Oligodendroglia pathology
Subjects
Details
- Language :
- English
- ISSN :
- 0885-3185
- Volume :
- 15
- Issue :
- 5
- Database :
- MEDLINE
- Journal :
- Movement disorders : official journal of the Movement Disorder Society
- Publication Type :
- Academic Journal
- Accession number :
- 11009180
- Full Text :
- https://doi.org/10.1002/1531-8257(200009)15:5<784::aid-mds1004>3.0.co;2-p