Evidence map›Paper›PMID 23199590›Full record

Trial reportJournal of the neurological sciences2013

A randomized, controlled, delayed start trial of GM1 ganglioside in treated Parkinson's disease patients.

Jay S Schneider, Stephen M Gollomp, Stephanie Sendek, Amy Colcher, Franca Cambi, Wei Du

Abstract readRandomized Controlled Trial
In one paragraph

Trial report in Journal of the neurological sciences, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 84 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
84citing papers in PubMed, 1 pooled it
6.4field-weighted citation impact, top 3% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

84 citing papers in PubMed, 1 synthesis or guideline pooled it, 142 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Trial
  4. Gangliosides in molecular interactions and cell regulation.The Journal of biological chemistry · 2026
    Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Review
  10. Review
  11. Review
  12. Review
  13. Review
  14. Article
  15. Ganglioside GM1 and the Central Nervous System.International journal of molecular sciences · 2023
    Review
  16. Review
  17. Article
  18. Review
  19. Review
  20. Gangliosides in Neurodegenerative Diseases.Advances in neurobiology · 2023
    Article

24 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors at 3 institutions in 1 country.

Jay S SchneiderDept. of Pathology, Anatomy and Cell Biology and Parkinson's Disease Research Unit, Thomas Jefferson University, Philadelphia, PA 19107, USA. jay.schneider@jefferson.edu
Stephen M Gollomp
Stephanie Sendek
Amy Colcher
Franca Cambi
Wei Du
Thomas Jefferson University · USUniversity of Kentucky · USUniversity of Pennsylvania · US

Funding

GM1 GANGLIOSIDE EFFECTS ON PARKINSONS DISEASER01NS038681 · NINDS · THOMAS JEFFERSON UNIVERSITY · PI SCHNEIDER, JAY S · 1999 to 2007
$5.5M
NINDS NIH HHS NS038681NINDS NIH HHS R01 NS038681
6 · The paper itself

Abstract

The present single center, double-blind, delayed start study was conducted to examine possible symptomatic and disease-modifying effects of GM1 ganglioside in Parkinson's disease (PD). Seventy-seven subjects with PD were randomly assigned to receive GM1 for 120 weeks (early-start group) or placebo for 24 weeks followed by GM1 for 96 weeks (delayed-start group). Washout evaluations occurred at 1 and 2 years after the end of treatment. Seventeen additional subjects who received standard-of-care were followed for comparative information about disease progression. Primary outcome was change from baseline Unified Parkinson's Disease Rating Scale (UPDRS) motor scores. At week 24, the early-start group had significant improvement in UPDRS motor scores vs. a significant worsening of scores in the delayed-start group. The early-start group also showed a sustained benefit vs. the delayed-start group at week 72 and at week 120. Both groups had significant symptom worsening during washout. This study provides evidence that GM1 use for 24 weeks was superior to placebo for improving motor symptoms and that extended GM1 use (up to 120 weeks) resulted in a lower than expected rate of symptom progression. The data from this small study suggest that GM1 may have symptomatic and potentially disease modifying effects on PD.

Indexed as

Analysis of VarianceAntiparkinson AgentsDisease ProgressionDopamine AgonistsDouble-Blind MethodFemaleFollow-Up StudiesG(M1) GangliosideHumansMaleMiddle AgedNeuropsychological TestsParkinson DiseaseTreatment OutcomeAntiparkinson AgentsDopamine AgonistsG(M1) Ganglioside

Identifiers

PMID23199590
PMCPMC3532888
OpenAlexW2110127543

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.