The pathogenesis of multiple system atrophy: Past, present, and future
Identifieur interne : 007237 ( Main/Merge ); précédent : 007236; suivant : 007238The pathogenesis of multiple system atrophy: Past, present, and future
Auteurs : Evelyn Jaros [Royaume-Uni] ; David J. Burn [Royaume-Uni]Source :
- Movement Disorders [ 0885-3185 ] ; 2000-09.
English descriptors
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 α‐synuclein accumulation in these inclusions. The latter finding links multiple system atrophy as an “α‐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.
Url:
DOI: 10.1002/1531-8257(200009)15:5<784::AID-MDS1004>3.0.CO;2-P
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ISTEX:C58766726A53DEE4F4832254D08A7EB034AE2028Le document en format XML
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<front><div type="abstract" xml:lang="en">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 α‐synuclein accumulation in these inclusions. The latter finding links multiple system atrophy as an “α‐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.</div>
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