Evidence map›Paper›PMID 26769912›Full record

ArticleThe Journal of endocrinology2016

Endogenous GLP1 and GLP1 analogue alter CNS responses to palatable food consumption.

Jennifer S Ten Kulve, Dick J Veltman, Liselotte van Bloemendaal, Paul F C Groot, Henricus G Ruhé, Frederik Barkhof, Michaela Diamant, Richard G Ijzerman

Registry-linked trialOpen access · bronzeAbstract read
PubMed Publisher
In one paragraph

Article in The Journal of endocrinology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT03361098 (Combined Effects of SGLT2 Inhibition and GLP-1 Receptor Agonism on Food Intake, Body Weight and Central Satiety and Reward Circuits in Obese T2DM Patients), which is not on this map. Cited by 41 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed, 3 pooled it
2.9field-weighted citation impact, top 9% 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.

NCT03361098 phase4completedstarted 2017, after this paper: background citation

Combined Effects of SGLT2 Inhibition and GLP-1 Receptor Agonism on Food Intake, Body Weight and Central Satiety and Reward Circuits in Obese T2DM Patients

Ran2017Enrolled65Registered outcomes18Posted comparisons0ConditionsObesity, Type 2 Diabetes MellitusArmsDapagliflozin 10mg, exenatide, placebo dapagliflozin, placebo exenatide
Open the trial in the graph
3 · Its place in the literature

Who cites it

41 citing papers in PubMed, 3 syntheses or guidelines pooled it, 66 citations in OpenAlex.

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  12. Sex Differences in [Diabetes, obesity & metabolism · 2026
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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

8 authors at 3 institutions in 1 country.

Jennifer S Ten KulveDiabetes Center/Department of Internal MedicineVU University Medical Center, Amsterdam, The Netherlands js.tenkulve@vumc.nl.
Dick J VeltmanDepartment of PsychiatryVU University Medical Center, Amsterdam, The Netherlands.
Liselotte van BloemendaalDiabetes Center/Department of Internal MedicineVU University Medical Center, Amsterdam, The Netherlands.
Paul F C GrootDepartment of RadiologyAcademic Medical Center, Amsterdam, The Netherlands.
Henricus G RuhéDepartment of PsychiatryAcademic Medical Center, Amsterdam, The Netherlands University of GroningenUniversity Medical Center Groningen, Department of Psychiatry, Groningen, The Netherlands.
Frederik BarkhofDepartment of Radiology & Nuclear MedicineVU University Medical Center, Amsterdam, The Netherlands.
Michaela DiamantDiabetes Center/Department of Internal MedicineVU University Medical Center, Amsterdam, The Netherlands.
Richard G IjzermanDiabetes Center/Department of Internal MedicineVU University Medical Center, Amsterdam, The Netherlands.
Amsterdam UMC Location VUmc · NLAcademic Medical Center · NLUniversity of Groningen · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Glucagon-like peptide-1 (GLP1) affects appetite, supposedly mediated via the central nervous system (CNS). In this study, we investigate whether modulation of CNS responses to palatable food consumption may be a mechanism by which GLP1 contributes to the central regulation of feeding. Using functional MRI, we determined the effects of endogenous GLP1 and treatment with the GLP1 analogue liraglutide on CNS activation to chocolate milk receipt. Study 1 included 20 healthy lean individuals and 20 obese patients with type 2 diabetes (T2DM). Scans were performed on two occasions: during infusion of the GLP1 receptor antagonist exendin 9-39 (blocking actions of endogenous GLP1) and during placebo infusion. Study 2 was a randomised, cross-over intervention study carried out in 20 T2DM patients, comparing treatment with liraglutide to insulin, after 10 days and 12 weeks. Compared with lean individuals, T2DM patients showed reduced activation to chocolate milk in right insula (P = 0.04). In lean individuals, blockade of endogenous GLP1 effects inhibited activation in bilateral insula (P ≤ 0.03). Treatment in T2DM with liraglutide, vs insulin, increased activation to chocolate milk in right insula and caudate nucleus after 10 days (P ≤ 0.03); however, these effects ceased to be significant after 12 weeks. Our findings in healthy lean individuals indicate that endogenous GLP1 is involved in the central regulation of feeding by affecting central responsiveness to palatable food consumption. In obese T2DM, treatment with liraglutide may improve the observed deficit in responsiveness to palatable food, which may contribute to the induction of weight loss observed during treatment. However, no long-term effects of liraglutide were observed.

Indexed as

AppetiteBlood GlucoseCase-Control StudiesCentral Nervous SystemDiabetes Mellitus, Type 2EatingFemaleGlucagon-Like Peptide 1HumansLiraglutideMagnetic Resonance ImagingMaleMiddle AgedObesityPeptide FragmentsBlood Glucoseexendin (9-39)Glucagon-Like Peptide 1LiraglutidePeptide FragmentsfMRIGLP1obesitypalatable foodtype 2 diabetes

Identifiers

PMID26769912
OpenAlexW2340188550

What Socratic holds

Texttitle and abstract
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 Socratic graph.