Evidence map›Paper›PMID 8897012›Full record

Trial reportDiabetologia1996

GLP-1 does not not acutely affect insulin sensitivity in healthy man.

L Orskov, J J Holst, J Møller, C Orskov, N Møller, K G Alberti, O Schmitz

Registry-linked trialAbstract readClinical TrialControlled Clinical Trial
PubMed Publisher
In one paragraph

Trial report in Diabetologia, 1996. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT01159847 (Protective Effects of Sitagliptin on β Cell Function in Patients With Adult-onset Latent Autoimmune Diabetes), which is not on this map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
4.0field-weighted citation impact, top 6% 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.

NCT01159847 phase1 / phase2completednot on this mapstarted 2010, after this paper: background citation

Protective Effects of Sitagliptin on β Cell Function in Patients With Adult-onset Latent Autoimmune Diabetes (LADA)

TypeinterventionalSponsorEuropean Foundation for the Study of DiabetesRan2010 to 2012Enrolled30ConditionsType 1 DiabetesArmssitagliptin, Insulin
3 · Its place in the literature

Who cites it

25 citing papers in PubMed, 116 citations in OpenAlex.

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  6. Effects of Glucagon-Like Peptide-1 Receptor Agonists (Mono and Combination Therapy) on Energy Expenditure: A Scoping Review.Obesity reviews : an official journal of the International Association for the Study of Obesity · 2026
    Article
  7. Review
  8. 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
    Review
  9. Article
  10. Review
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  12. Effects of intraportal exenatide on hepatic glucose metabolism in the conscious dog.American journal of physiology. Endocrinology and metabolism · 2013
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  13. Article
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  16. Neonatal exendin-4 treatment reduces oxidative stress and prevents hepatic insulin resistance in intrauterine growth-retarded rats.American journal of physiology. Regulatory, integrative and comparative physiology · 2009
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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 3 institutions in 2 countries.

L OrskovInstitute of Experimental Clinical Research Arhus University Hospital, Denmark.
J J Holst
J Møller
C Orskov
N Møller
K G Alberti
O Schmitz
Aarhus University Hospital · DKUniversity of Copenhagen · DKNewcastle University · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Previous studies have suggested that glucagon-like peptide-1 (GLP-1) (7-36 amide) may have the direct effect of increasing insulin sensitivity in healthy man. To evaluate this hypothesis we infused GLP-1 in seven lean healthy men during a hyper insulinaemic (0.8 mU.kg-1.min-1), euglycaemic (5 mmol/l) clamp. Somatostatin (450 micrograms/h was infused to suppress endogenous insulin secretion, and growth hormone (3 ng.kg-1.min-1) and glucagon (0.8 ng.kg-1.min-1) were infused to maintain basal levels. GLP-1 (50 pmol.kg-1.h-1) or 154 mmol/l NaCl (placebo) was infused after 3 h of equilibration, i.e. from 180-360 min. GLP-1 infusion resulted in GLP-1 levels of approximately 40 pmol/l. Plasma glucose, insulin, growth hormone, and glucagon levels were similar throughout the clamps. The rate of glucose infusion required to maintain euglycaemia was similar with or without GLP-1 infusion (7.69 +/- 1.17 vs 7.76 +/- 0.95 mg kg-1.min-1 at 150-180 min and 8.56 +/- 1.13 vs 8.55 +/- 0.68 mg.kg-1.min-1 at 330-360 min) and there was no difference in isotopically determined hepatic glucose production rates (-0.30 +/- 0.23 vs -0.16 +/- 0.22 mg.kg-1.min-1 at 330-360 min). Furthermore, arteriovenous glucose differences across the forearm were similar with or without GLP-1 infusion (1.43 +/- 0.23 vs 1.8 +/- 0.29 mmol/l), (ANOVA; p > 0.60, in all instances). In conclusion, GLP-1 (7-36 amide) administered for 3 h, leading to circulating levels within the physiological range, does not affect insulin sensitivity in healthy man.

Indexed as

3-Hydroxybutyric AcidAdultAlanineAnalysis of VarianceBlood GlucoseCalorimetry, IndirectC-PeptideFatty Acids, NonesterifiedGlucagonGlucagon-Like Peptide 1Glucagon-Like PeptidesGlucose Clamp TechniqueHumansHydroxybutyratesInfusions, IntravenousInsulin3-Hydroxybutyric AcidAlanineBlood GlucoseC-PeptideFatty Acids, NonesterifiedGlucagonGlucagon-Like Peptide 1glucagon-like peptide 1 (7-36)amideGlucagon-Like PeptidesHydroxybutyratesInsulinLactatesNeurotransmitter AgentsPeptide FragmentsSomatostatin

Identifiers

PMID8897012
OpenAlexW1995482720

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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.