GM1 ganglioside treatment of Parkinson's disease: an open pilot study of safety and efficacy.

Abstract:

:We performed an open-label study testing the effects of GM1 ganglioside on 10 Parkinson's disease (PD) patients. Patients received 1,000 mg of GM1 by IV infusion after the last of three baseline functional assessments. Patients then self-administered GM1 at a dose of 200 mg/d, by subcutaneous injection, for 18 weeks. Under these conditions, GM1 ganglioside proved to be safe and well tolerated. There were no serious adverse events and none of the patients developed elevated anti-GM1 antibody titers. Improvements on at least some functional measures were present in most patients, beginning after 4 to 8 weeks of GM1 treatment. When functional improvements occurred, they lasted for the duration of the study. These results suggest that GM1 ganglioside is well tolerated and may be a useful adjunct to the treatment of PD, and that a double-blind, placebo-controlled study is now warranted.

journal_name

Neurology

journal_title

Neurology

authors

Schneider JS,Roeltgen DP,Rothblat DS,Chapas-Crilly J,Seraydarian L,Rao J

doi

10.1212/wnl.45.6.1149

subject

Has Abstract

pub_date

1995-06-01 00:00:00

pages

1149-54

issue

6

eissn

0028-3878

issn

1526-632X

journal_volume

45

pub_type

临床试验,杂志文章
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    pub_type: 临床试验,杂志文章

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    doi:10.1212/WNL.0000000000002238

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    doi:10.1212/01.wnl.0000277455.08067.9c

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    pub_type: 杂志文章

    doi:10.1212/WNL.0000000000003696

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