The North American Multiple System Atrophy Study Group

被引:64
作者
Gilman, S
May, SJ
Shults, CW
Tanner, CM
Kukull, W
Lee, VMY
Masliah, E
Low, P
Sandroni, P
Trojanowski, JQ
Ozelius, L
Foroud, T
机构
[1] Univ Michigan, Dept Neurol, Ann Arbor, MI 48109 USA
[2] Univ Calif San Diego, Dept Family & Prevent Med, La Jolla, CA 92093 USA
[3] VA San Diego Healthcare Syst, San Diego, CA USA
[4] Parkinsons Inst, Dept Clin Res, Sunnyvale, CA USA
[5] Univ Washington, Dept Epidemiol, Seattle, WA 98195 USA
[6] Univ Penn, Dept Pathol & Lab Med, Ctr Neurol Dis Res, Philadelphia, PA 19104 USA
[7] Univ Calif San Diego, Dept Neurosci, La Jolla, CA 92093 USA
[8] Mayo Clin, Dept Neurol, Rochester, MA USA
[9] Albert Einstein Coll Med, Dept Mol Genet, Bronx, NY 10467 USA
[10] Indiana Univ, Sch Med, Dept Med & Mol Genet, Indianapolis, IN 46204 USA
关键词
multiple system atrophy; parkinsonism; cerebellar ataxia; autonomic failure;
D O I
10.1007/s00702-005-0381-6
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
The North American Multiple System Atrophy Study Group involves investigators in 12 US medical centers funded by a grant from the National Institutes of Health. The objectives are to examine the environmental and genetic risk factors for MSA; elucidate pathogenic mechanisms underlying the disorder; and refine evaluations used for assessment. During its first year, the group enrolled 87 patients, implemented four cores, and initiated four scientific projects. Most patients among the 87 had parkinsonian features, which frequently began asymmetrically and remained asymmetrical; one-third responded to levodopa and many developed levodopa complications; almost two-thirds of the patients had cerebellar dysfunction, of these 90% had ataxia; urinary incontinence occurred commonly, and sleep disorders affected most. The investigators studied the effects of oxidative and nitrative stress upon the formation of alpha-synuclein inclusions; generated transgenic models of alpha-synuclein accumulation that recapitulate several behavioral and neuropathological features of MSA; and compared the severity of the autonomic features of MSA, Parkinson's disease and dementia with Lewy bodies.
引用
收藏
页码:1687 / 1694
页数:8
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