Evidence map›Paper›PMID 38127286›Full record

ReviewDrugs2024

Poly-Agonist Pharmacotherapies for Metabolic Diseases: Hopes and New Challenges.

Camille Allard, Daniela Cota, Carmelo Quarta

Abstract readReview
PubMed Publisher
In one paragraph

Review in Drugs, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
3.0field-weighted citation impact, top 7% 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

9 citing papers in PubMed, 15 citations in OpenAlex.

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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

3 authors at 1 institution in 1 country.

Camille AllardUniversity of Bordeaux, INSERM, Neurocentre Magendie, U1215, 33000, Bordeaux, France.ORCID http://orcid.org/0000-0002-2198-6011
Daniela CotaUniversity of Bordeaux, INSERM, Neurocentre Magendie, U1215, 33000, Bordeaux, France.ORCID http://orcid.org/0000-0002-6909-2156
Carmelo QuartaUniversity of Bordeaux, INSERM, Neurocentre Magendie, U1215, 33000, Bordeaux, France. carmelo.quarta@inserm.fr.ORCID http://orcid.org/0000-0002-1352-4239
Université de Bordeaux · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The use of glucagon-like peptide-1 (GLP-1) receptor-based multi-agonists in the treatment of type 2 diabetes and obesity holds great promise for improving glycaemic control and weight management. Unimolecular dual and triple agonists targeting multiple gut hormone-related pathways are currently in clinical trials, with recent evidence supporting their efficacy. However, significant knowledge gaps remain regarding the biological mechanisms and potential adverse effects associated with these multi-target agents. The mechanisms underlying the therapeutic efficacy of GLP-1 receptor-based multi-agonists remain somewhat mysterious, and hidden threats may be associated with the use of gut hormone-based polyagonists. In this review, we provide a critical analysis of the benefits and risks associated with the use of these new drugs in the management of obesity and diabetes, while also exploring new potential applications of GLP-1-based pharmacology beyond the field of metabolic disease.

Indexed as

Diabetes Mellitus, Type 2Metabolic DiseasesGlucagon-Like Peptide 1Glucagon-Like Peptide-1 ReceptorHumansHypoglycemic AgentsObesityGlucagon-Like Peptide 1Glucagon-Like Peptide-1 ReceptorHypoglycemic Agents

Identifiers

PMID38127286
OpenAlexW4390070643

What OpenQuestion holds

Textmetadata
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.