Evidence map›Paper›PMID 32412796›Full record

ReviewExpert opinion on investigational drugs2020

Glucagon-like peptide-1 (GLP-1)-based receptor agonists as a treatment for Parkinson's disease.

Elliot J Glotfelty, Lars Olson, Tobias E Karlsson, Yazhou Li, Nigel H Greig

Open access · greenAbstract readReview
In one paragraph

Review in Expert opinion on investigational drugs, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed, 3 pooled it
4.5field-weighted citation impact, top 4% 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

43 citing papers in PubMed, 3 syntheses or guidelines pooled it, 58 citations in OpenAlex.

  1. Pooled it
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  3. GLP-1a: Going beyond Traditional Use.International journal of molecular sciences · 2022
    Pooled it
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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

5 authors at 2 institutions in 2 countries.

Elliot J GlotfeltyTranslational Gerontology Branch, Intramural Research Program, National Institute on Aging, National Institutes of Health , Baltimore, MD, USA.
Lars OlsonDepartment of Neuroscience, Karolinska Institutet , Stockholm, Sweden.
Tobias E KarlssonDepartment of Neuroscience, Karolinska Institutet , Stockholm, Sweden.
Yazhou LiTranslational Gerontology Branch, Intramural Research Program, National Institute on Aging, National Institutes of Health , Baltimore, MD, USA.
Nigel H GreigTranslational Gerontology Branch, Intramural Research Program, National Institute on Aging, National Institutes of Health , Baltimore, MD, USA.ORCID https://orcid.org/0000-0002-3032-1468
National Institutes of Health · USKarolinska Institutet · SE

Funding

Neuroprotective role of GLP-1 receptor agonists (Neurodegenerative disorders & Alzheimer's disease)ZIAAG000333 · NIA · NATIONAL INSTITUTE ON AGING · PI GREIG, NIGEL H. · 2009 to 2025
$10.9M
Intramural NIH HHS Z99 AG999999Intramural NIH HHS ZIA AG000333
6 · The paper itself

Abstract

introductionAccumulating evidence supports the evaluation of glucagon-like peptide-1 (GLP-1) receptor (R) agonists for the treatment of the underlying pathology causing Parkinson's Disease (PD). Not only are these effects evident in models of PD and other neurodegenerative disorders but recently in a randomized, double-blind, placebo-controlled clinical trial, a GLP-1R agonist has provided improved cognition motor functions in humans with moderate PD. AREAS COVERED: In this mini-review, we describe the development of GLP-1R agonists and their potential therapeutic value in treating PD. Many GLP-1R agonists are FDA approved for the treatment of metabolic disorders, and hence can be rapidly repositioned for PD. Furthermore, we present preclinical data offering insights into the use of monomeric dual- and tri-agonist incretin-based mimetics for neurodegenerative disorders. These drugs combine active regions of GLP-1 with those of glucose-dependent insulinotropic peptide (GIP) and/or glucagon (Gcg). EXPERT OPINION: GLP-1Ragonists offer a complementary and enhanced therapeutic value to other drugs used to treat PD. Moreover, the use of the dual- or tri-agonist GLP-1-based mimetics may provide combinatory effects that are even more powerful than GLP-1R agonism alone. We advocate for further investigations into the repurposing of GLP-1R agonists and the development of classes of multi-agonists for PD treatment.

Indexed as

Glucagon-Like Peptide-1 Receptor AgonistsAnimalsAntiparkinson AgentsDrug DevelopmentDrug RepositioningHumansNeurodegenerative DiseasesParkinson DiseaseRandomized Controlled Trials as TopicAntiparkinson AgentsGlucagon-Like Peptide-1 Receptor Agonistsbrain traumaglucagon (Gcg)Glucagon-like peptide-1 (GLP-1)glucose-dependent insulinotropic peptide (GIP)incretin mimeticsmicroglianeurodegenerationParkinson’s disease

Identifiers

PMID32412796
PMCPMC10477949
OpenAlexW3025383706

What Socratic 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 Socratic graph.