Evidence map›Paper›PMID 29938884›Full record

ArticleDiabetes, obesity & metabolism2018

Running on mixed fuel-dual agonistic approach of GLP-1 and GCG receptors leads to beneficial impact on body weight and blood glucose control: A comparative study between mice and non-human primates.

Ralf Elvert, Andreas W Herling, Martin Bossart, Tilo Weiss, Baohong Zhang, Pierre Wenski, Jörn Wandschneider, Sabrina Kleutsch, Uwe Butty, Aimo Kannt and 7 more

Open access · bronzeAbstract readComparative Study
In one paragraph

Article in Diabetes, obesity & metabolism, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
2.4field-weighted citation impact, top 10% 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

18 citing papers in PubMed, 40 citations in OpenAlex.

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  12. The incretin/glucagon system as a target for pharmacotherapy of obesity.Obesity reviews : an official journal of the International Association for the Study of Obesity · 2022 · on this map
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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

17 authors at 2 institutions in 1 country.

Ralf ElvertSanofi-Aventis Deutschland GmbH, Frankfurt, Germany.ORCID http://orcid.org/0000-0003-1216-307X
Andreas W HerlingSanofi-Aventis Deutschland GmbH, Frankfurt, Germany.
Martin BossartSanofi-Aventis Deutschland GmbH, Frankfurt, Germany.
Tilo WeissSanofi-Aventis Deutschland GmbH, Frankfurt, Germany.
Baohong ZhangKunming Biomed International, Yunnan, China.
Pierre WenskiSanofi-Aventis Deutschland GmbH, Frankfurt, Germany.
Jörn WandschneiderSanofi-Aventis Deutschland GmbH, Frankfurt, Germany.
Sabrina KleutschSanofi-Aventis Deutschland GmbH, Frankfurt, Germany.
Uwe ButtySanofi-Aventis Deutschland GmbH, Frankfurt, Germany.
Aimo KanntSanofi-Aventis Deutschland GmbH, Frankfurt, Germany.
Michael WagnerSanofi-Aventis Deutschland GmbH, Frankfurt, Germany.
Torsten HaackSanofi-Aventis Deutschland GmbH, Frankfurt, Germany.
Andreas EversSanofi-Aventis Deutschland GmbH, Frankfurt, Germany.
Angela DuddaSanofi-Aventis Deutschland GmbH, Frankfurt, Germany.
Martin LorenzSanofi-Aventis Deutschland GmbH, Frankfurt, Germany.
Stefanie KeilSanofi-Aventis Deutschland GmbH, Frankfurt, Germany.
Philip J LarsenSanofi-Aventis Deutschland GmbH, Frankfurt, Germany.
Sanofi (Germany) · DEHeidelberg University · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimWe performed acute and chronic studies in healthy and diet-induced obese animals using mouse-specific or monkey-specific dual GLP-1R/GCGR agonists to investigate their effects on food intake, body weight, blood glucose control and insulin secretion. The selective GLP-1R agonist liraglutide was used as comparator.

methodsThe mouse-specific dual agonist and liraglutide were tested in lean wild type, GLP-1R knockout and diet-induced obese mice at different doses. A chronic study was performed in DIO mice to investigate the effect on body weight, food consumption and total energy expenditure (TEE) in obese and diabetic monkeys with a focus on body weight and energy intake.

resultsThe mouse-specific dual agonist and liraglutide similarly affected glycaemic control. A higher loss in body weight was measured in dual agonist-treated obese mice. The dual agonist significantly enhanced plasma glucose excursion in overnight fed GLP-1R

conclusionsIn DIO mice and non-human primates, dual agonists elicited robust glycaemic control, similar to the marketed GLP-1R agonist, while eliciting greater effects on body weight. Results from DIO mice suggest that the increase in TEE is caused not only by increased fat oxidation but also by an increase in carbohydrate oxidation.

Indexed as

Glucagon-Like Peptide-1 Receptor AgonistsAnimalsAnimals, Outbred StrainsAppetite DepressantsBody WeightDiabetes Mellitus, Type 2Diet, High-FatDose-Response Relationship, DrugDrug Therapy, CombinationEnergy IntakeEnergy MetabolismFemaleGlucagon-Like Peptide-1 ReceptorHyperglycemiaHypoglycemic AgentsInsulin SecretionAppetite DepressantsGlucagon-Like Peptide-1 ReceptorGlucagon-Like Peptide-1 Receptor AgonistsHypoglycemic AgentsReceptors, Glucagondiabetesdiet-induced obesitydual agonism, energy expenditureGLP-1glucagonmousenon-human primates

Identifiers

PMID29938884
PMCPMC6055720
OpenAlexW2810819338

What OpenQuestion holds

Textmetadata
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 OpenQuestion graph.