Evidence map›Paper›PMID 35054924›Full record

ReviewInternational journal of molecular sciences2022

GLP-1a: Going beyond Traditional Use.

Lucas Fornari Laurindo, Sandra Maria Barbalho, Elen Landgraf Guiguer, Maricelma da Silva Soares de Souza, Gabriela Achete de Souza, Thiago Marques Fidalgo, Adriano Cressoni Araújo, Heron F de Souza Gonzaga, Daniel de Bortoli Teixeira, Thais de Oliveira Silva Ullmann and 2 more

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 46 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
46citing papers in PubMed, 1 pooled it
12.4field-weighted citation impact, top 1% 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

46 citing papers in PubMed, 1 synthesis or guideline pooled it, 92 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Review
  4. Review
  5. Review
  6. Article
  7. Frontiers in aging neuroscience · 2026
    Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Review
  13. Article
  14. Review
  15. Article
  16. Advances in GLP-1 receptor agonists for pain treatment and their future potential.The journal of headache and pain · 2025 · on this map
    Review
  17. Review
  18. Review
  19. Spotlight on the Mechanism of Action of Semaglutide.Current issues in molecular biology · 2024
    Review
  20. Article
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

12 authors at 4 institutions in 2 countries.

Lucas Fornari LaurindoDepartment of Biochemistry and Pharmacology, School of Medicine, University of Marília, Avenida Higino Muzzi Filho, Marília 17525-902, SP, Brazil.ORCID 0000-0003-3159-0982
Sandra Maria BarbalhoDepartment of Biochemistry and Pharmacology, School of Medicine, University of Marília, Avenida Higino Muzzi Filho, Marília 17525-902, SP, Brazil.ORCID 0000-0002-5035-876X
Elen Landgraf GuiguerDepartment of Biochemistry and Pharmacology, School of Medicine, University of Marília, Avenida Higino Muzzi Filho, Marília 17525-902, SP, Brazil.ORCID 0000-0002-9930-9694
Maricelma da Silva Soares de SouzaDepartment of Biochemistry and Pharmacology, School of Medicine, University of Marília, Avenida Higino Muzzi Filho, Marília 17525-902, SP, Brazil.
Gabriela Achete de SouzaDepartment of Biochemistry and Pharmacology, School of Medicine, University of Marília, Avenida Higino Muzzi Filho, Marília 17525-902, SP, Brazil.
Thiago Marques FidalgoDepartment of Psychiatry, Federal University of São Paulo, R. Sena Madureira 04021-001, SP, Brazil.
Adriano Cressoni AraújoDepartment of Biochemistry and Pharmacology, School of Medicine, University of Marília, Avenida Higino Muzzi Filho, Marília 17525-902, SP, Brazil.ORCID 0000-0002-5716-2444
Heron F de Souza GonzagaDepartment of Biochemistry and Pharmacology, School of Medicine, University of Marília, Avenida Higino Muzzi Filho, Marília 17525-902, SP, Brazil.
Daniel de Bortoli TeixeiraPostgraduate Program in Animal Health, Production and Environment, University of Marilia, Marília 17525-902, SP, Brazil.
Thais de Oliveira Silva UllmannDepartment of Biochemistry and Pharmacology, School of Medicine, University of Marília, Avenida Higino Muzzi Filho, Marília 17525-902, SP, Brazil.
Katia Portero SloanTexas Institute for Kidney and Endocrine Disorders, Lufkin, TX 75904, USA.
Lance Alan SloanTexas Institute for Kidney and Endocrine Disorders, Lufkin, TX 75904, USA.
Universidade de Marília · BRFaculdade de Medicina de Marília · BRLankenau Institute for Medical Research · USUniversidade Federal de São Paulo · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Glucagon-like peptide-1 (GLP-1) is a human incretin hormone derived from the proglucagon molecule. GLP-1 receptor agonists are frequently used to treat type 2 diabetes mellitus and obesity. However, the hormone affects the liver, pancreas, brain, fat cells, heart, and gastrointestinal tract. The objective of this study was to perform a systematic review on the use of GLP-1 other than in treating diabetes. PubMed, Cochrane, and Embase were searched, and the PRISMA guidelines were followed. Nineteen clinical studies were selected. The results showed that GLP-1 agonists can benefit defined off-medication motor scores in Parkinson's Disease and improve emotional well-being. In Alzheimer's disease, GLP-1 analogs can improve the brain's glucose metabolism by improving glucose transport across the blood-brain barrier. In depression, the analogs can improve quality of life and depression scales. GLP-1 analogs can also have a role in treating chemical dependency, inhibiting dopaminergic release in the brain's reward centers, decreasing withdrawal effects and relapses. These medications can also improve lipotoxicity by reducing visceral adiposity and decreasing liver fat deposition, reducing insulin resistance and the development of non-alcoholic fatty liver diseases. The adverse effects are primarily gastrointestinal. Therefore, GLP-1 analogs can benefit other conditions besides traditional diabetes and obesity uses.

Indexed as

Clinical Trials as TopicDiabetes Mellitus, Type 2Disease ManagementGlucagon-Like Peptide 1Glucagon-Like Peptide-1 Receptor AgonistsHumansNeurodegenerative DiseasesObesityPeptide FragmentsTreatment OutcomeGlucagon-Like Peptide 1glucagon-like peptide 1 (7-36)amideGlucagon-Like Peptide-1 Receptor AgonistsPeptide FragmentsAlzheimer’s diseasedepressiondiabetesglucagon-like peptide-1non-alcoholic fatty liver diseaseobesityParkinson’s diseasevisceral insulin resistance adiposity syndrome

Identifiers

PMID35054924
PMCPMC8775408
OpenAlexW4205935861

What Socratic holds

Textmetadata
LicenceCC BY
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.