Evidence map›Paper›PMID 39353946›Full record

ArticleNature communications2024

Superior metabolic improvement of polycystic ovary syndrome traits after GLP1-based multi-agonist therapy.

Miguel A Sánchez-Garrido, Víctor Serrano-López, Francisco Ruiz-Pino, María Jesús Vázquez, Andrea Rodríguez-Martín, Encarnación Torres, Inmaculada Velasco, Ana Belén Rodríguez, Eduardo Chicano-Gálvez, Marina Mora-Ortiz and 11 more

Abstract read
In one paragraph

Article in Nature communications, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
–field-weighted citation impact
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

31 citing papers in PubMed.

  1. Article
  2. The Role and Mechanism of Incretins in Gynaecologic Diseases.Endocrinology, diabetes & metabolism · 2026
    Review
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  4. Review
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  6. Review
  7. Review
  8. Article
  9. Review
  10. Review
  11. Article
  12. Article
  13. Review
  14. Living with PCOS: A Narrative of its Biology, Diagnosis, and Evolving Treatment.Endocrine, metabolic & immune disorders drug targets · 2026
    Review
  15. Article
  16. Article
  17. Article
  18. Review
  19. Article
  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

21 authors.

Miguel A Sánchez-Garrido *Instituto Maimónides de Investigación Biomédica de Córdoba (IMIBIC), Córdoba, Spain. b12sanom@uco.es.ORCID 0000-0002-1010-5012
Víctor Serrano-López *Instituto Maimónides de Investigación Biomédica de Córdoba (IMIBIC), Córdoba, Spain.
Francisco Ruiz-PinoInstituto Maimónides de Investigación Biomédica de Córdoba (IMIBIC), Córdoba, Spain.
María Jesús VázquezInstituto Maimónides de Investigación Biomédica de Córdoba (IMIBIC), Córdoba, Spain.
Andrea Rodríguez-MartínInstituto Maimónides de Investigación Biomédica de Córdoba (IMIBIC), Córdoba, Spain.
Encarnación TorresInstituto Maimónides de Investigación Biomédica de Córdoba (IMIBIC), Córdoba, Spain.
Inmaculada VelascoInstituto Maimónides de Investigación Biomédica de Córdoba (IMIBIC), Córdoba, Spain.
Ana Belén RodríguezDepartment of Cell Biology, Physiology and Immunology, University of Córdoba, Córdoba, Spain.
Eduardo Chicano-GálvezInstituto Maimónides de Investigación Biomédica de Córdoba (IMIBIC), Córdoba, Spain.
Marina Mora-OrtizInstituto Maimónides de Investigación Biomédica de Córdoba (IMIBIC), Córdoba, Spain.ORCID 0000-0002-6662-2932
Claes OhlssonCentre for Bone and Arthritis Research, Institute of Medicine, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden.ORCID 0000-0002-9633-2805
Matti PoutanenCentre for Bone and Arthritis Research, Institute of Medicine, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden.
Leonor PinillaInstituto Maimónides de Investigación Biomédica de Córdoba (IMIBIC), Córdoba, Spain.
Francisco GaytánInstituto Maimónides de Investigación Biomédica de Córdoba (IMIBIC), Córdoba, Spain.
Jonathan D DourosNovo Nordisk Research Center Indianapolis, Indianapolis, IN, USA.
Bin YangNovo Nordisk Research Center Indianapolis, Indianapolis, IN, USA.
Timo D MüllerInstitute for Diabetes and Obesity, Helmholtz Zentrum München, Neuherberg, Germany.
Richard D DiMarchiDepartment of Chemistry, Indiana University, Bloomington, IN, USA.ORCID 0000-0003-0220-4085
Matthias H TschöpInstitute for Diabetes and Obesity, Helmholtz Zentrum München, Neuherberg, Germany.ORCID 0000-0002-4744-371X
Brian FinanNovo Nordisk Research Center Indianapolis, Indianapolis, IN, USA.
Manuel Tena-SempereInstituto Maimónides de Investigación Biomédica de Córdoba (IMIBIC), Córdoba, Spain. fi1tesem@uco.es.ORCID 0000-0002-4741-5567

Funding

Ministry of Economy and Competitiveness | Agencia Estatal de Investigación (Spanish Agencia Estatal de Investigación) BFU2017-83934-PMinistry of Economy and Competitiveness | Agencia Estatal de Investigación (Spanish Agencia Estatal de Investigación) PID2020-118660GB-I00Ministry of Economy and Competitiveness | Instituto de Salud Carlos III (Institute of Health Carlos III) PIE14-00005
6 · The paper itself

Abstract

Polycystic ovary syndrome (PCOS) is a heterogeneous condition, defined by oligo-/anovulation, hyper-androgenism and/or polycystic ovaries. Metabolic complications are common in patients suffering PCOS, including obesity, insulin resistance and type-2 diabetes, which severely compromise the clinical course of affected women. Yet, therapeutic options remain mostly symptomatic and of limited efficacy for the metabolic and reproductive alterations of PCOS. We report here the hormonal, metabolic and gonadal responses to the glucagon-like peptide-1 (GLP1)-based multi-agonists, GLP1/Estrogen (GLP1/E), GLP1/gastric inhibitory peptide (GLP1/GIP) and GLP1/GIP/Glucagon, in two mouse PCOS models, with variable penetrance of metabolic and reproductive traits, and their comparison with metformin. Our data illustrate the superior efficacy of GLP1/E vs. other multi-agonists and metformin in the management of metabolic complications of PCOS; GLP1/E ameliorates also ovarian cyclicity in an ovulatory model of PCOS, without direct estrogenic uterotrophic effects. In keeping with GLP1-mediated brain targeting, quantitative proteomics reveals changes in common and distinct hypothalamic pathways in response to GLP1/E between the two PCOS models, as basis for differential efficiency. Altogether, our data set the basis for the use of GLP1-based multi-agonists, and particularly GLP1/E, in the personalized management of PCOS.

Indexed as

Disease Models, AnimalGlucagon-Like Peptide 1MetforminPolycystic Ovary SyndromeAnimalsEstrogensFemaleGastric Inhibitory PolypeptideHumansInsulin ResistanceMiceMice, Inbred C57BLOvaryEstrogensGastric Inhibitory PolypeptideGlucagon-Like Peptide 1Metformin

Identifiers

PMID39353946
PMCPMC11445520

What Socratic holds

Texttitle and abstract
LicenceCC BY-NC-ND
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.