Evidence map›Paper›PMID 33822469›Full record

Trial reportDiabetes, obesity & metabolism2021

Improved postprandial glucose metabolism in type 2 diabetes by the dual glucagon-like peptide-1/glucagon receptor agonist SAR425899 in comparison with liraglutide.

Michele Schiavon, Roberto Visentin, Britta Göbel, Michela Riz, Claudio Cobelli, Thomas Klabunde, Chiara Dalla Man

Open access · hybridAbstract readRandomized Controlled Trial
In one paragraph

Trial report in Diabetes, obesity & metabolism, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed, 2 pooled it
5.1field-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

27 citing papers in PubMed, 2 syntheses or guidelines pooled it, 46 citations in OpenAlex.

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  16. The Current and Future Role of Insulin Therapy in the Management of Type 2 Diabetes: A Narrative Review.Diabetes therapy : research, treatment and education of diabetes and related disorders · 2024
    Review
  17. Article
  18. Article
  19. Future therapies for obesity.Clinical medicine (London, England) · 2023
    Review
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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

7 authors at 2 institutions in 3 countries.

Michele SchiavonDepartment of Information Engineering, University of Padova, Padova, Italy.ORCID 0000-0003-0590-2399
Roberto VisentinDepartment of Information Engineering, University of Padova, Padova, Italy.ORCID 0000-0002-5848-5990
Britta GöbelR&D Data & Data Science, Sanofi-Aventis Deutschland GmbH, Frankfurt am Main, Germany.
Michela RizR&D Data & Data Science, Sanofi-Aventis Deutschland GmbH, Frankfurt am Main, Germany.
Claudio CobelliDepartment of Information Engineering, University of Padova, Padova, Italy.
Thomas KlabundeR&D Data & Data Science, Sanofi-Aventis Deutschland GmbH, Frankfurt am Main, Germany.
Chiara Dalla ManDepartment of Information Engineering, University of Padova, Padova, Italy.ORCID 0000-0002-4908-0596
University of Padua · ITSanofi (France) · FR

Funding

MIUR (Italian Minister for Education) LAW 232/2016Sanofi
6 · The paper itself

Abstract

aimTo gain further insights into the efficacy of SAR425899, a dual glucagon-like peptide-1/glucagon receptor agonist, by providing direct comparison with the glucagon-like peptide-1 receptor agonist, liraglutide, in terms of key outcomes of glucose metabolism. RESEARCH DESIGN AND

methodsSeventy overweight to obese subjects with type 2 diabetes (T2D) were randomized to receive once-daily subcutaneous administrations of SAR425899 (0.12, 0.16 or 0.20 mg), liraglutide (1.80 mg) or placebo for 26 weeks. Mixed meal tolerance tests were conducted at baseline (BSL) and at the end of treatment (EOT). Metabolic indices of insulin action and secretion were assessed via Homeostasis Model Assessment (HOMA2) and oral minimal model (OMM) methods.

resultsFrom BSL to EOT (median [25th, 75th] percentile), HOMA2 quantified a significant improvement in basal insulin action in liraglutide (35% [21%, 74%]), while secretion enhanced both in SAR425899 (125% [63%, 228%]) and liraglutide (73% [43%, 147%]). OMM quantified, both in SAR425899 and liraglutide, a significant improvement in insulin sensitivity (203% [58%, 440%] and 36% [21%, 197%]), basal beta-cell responsiveness (67% [34%, 112%] and 40% [16%, 59%]), and above-basal beta-cell responsiveness (139% [64%, 261%] and 69% [-15%, 120%]). A significant delay in glucose absorption was highlighted in SAR425899 (37% [52%,18%]).

conclusionsSAR425899 and liraglutide improved postprandial glucose control in overweight to obese subjects with T2D. A significantly higher enhancement in beta-cell function was shown by SAR425899 than liraglutide.

Indexed as

Diabetes Mellitus, Type 2LiraglutideBlood GlucoseGlucagon-Like Peptide-1 ReceptorGlucoseHumansHypoglycemic AgentsInsulinReceptors, GlucagonBlood GlucoseGlucagon-Like Peptide-1 ReceptorGlucoseHypoglycemic AgentsInsulinLiraglutideReceptors, Glucagonbeta-cell functiondisposition indexdual agonistglucagonglucagon-like peptide-1insulin sensitivityliraglutidemixed meal tolerance testoral minimal model

Identifiers

PMID33822469
PMCPMC8359969
OpenAlexW3144177610

What Socratic holds

Texttitle and abstract
LicenceCC BY-NC
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.