Evidence map›Paper›PMID 29110715›Full record

ArticleCardiovascular diabetology2017

Liraglutide dictates macrophage phenotype in apolipoprotein E null mice during early atherosclerosis.

Robyn Bruen, Sean Curley, Sarina Kajani, Daniel Crean, Marcella E O'Reilly, Margaret B Lucitt, Catherine G Godson, Fiona C McGillicuddy, Orina Belton

Registry-linked trialOpen access · goldFull text read
In one paragraph

Article in Cardiovascular diabetology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT04137328 (Clinical Study on the Improvement of Diabetic Neuropathic Pain by Liraglutide), which is not on this map. Cited by 47 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
47citing papers in PubMed, 1 pooled it
3.4field-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.

NCT04137328 naunknown statusstarted 2019, after this paper: background citation

Clinical Study on the Improvement of Diabetic Neuropathic Pain by Liraglutide

Ran2019Enrolled60Registered outcomes3Posted comparisons0ConditionsDiabetic Neuropathic PainArmsInsulin, liraglutide
Open the trial in the graph
3 · Its place in the literature

Who cites it

47 citing papers in PubMed, 1 synthesis or guideline pooled it, 83 citations in OpenAlex.

  1. Exploring the Role of GLP-1 Agents in Managing Diabetic Foot Ulcers: A Narrative and Systematic Review.Wound repair and regeneration : official publication of the Wound Healing Society [and] the European Tissue Repair Society
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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

9 authors at 2 institutions in 1 country.

Robyn BruenDiabetes Complications Research Centre, School of Biomolecular and Biomedical Science, UCD Conway Institute, University College Dublin, Dublin 4, Ireland.
Sean CurleyDiabetes Complications Research Centre, School of Medicine, UCD Conway Institute, University College Dublin, Dublin 4, Ireland.
Sarina KajaniDiabetes Complications Research Centre, School of Medicine, UCD Conway Institute, University College Dublin, Dublin 4, Ireland.
Daniel CreanDiabetes Complications Research Centre, School of Veterinary Medicine, UCD Conway Institute, University College Dublin, Dublin 4, Ireland.
Marcella E O'ReillyDiabetes Complications Research Centre, School of Medicine, UCD Conway Institute, University College Dublin, Dublin 4, Ireland.
Margaret B LucittSchool of Medicine, Department of Pharmacology and Therapeutics, Trinity College Dublin, The University of Dublin, College Green, Dublin 2, Ireland.
Catherine G GodsonDiabetes Complications Research Centre, School of Medicine, UCD Conway Institute, University College Dublin, Dublin 4, Ireland.
Fiona C McGillicuddyDiabetes Complications Research Centre, School of Medicine, UCD Conway Institute, University College Dublin, Dublin 4, Ireland.
Orina BeltonDiabetes Complications Research Centre, School of Biomolecular and Biomedical Science, UCD Conway Institute, University College Dublin, Dublin 4, Ireland. orina.belton@ucd.ie.ORCID 0000-0002-7701-6540
University College Dublin · IETrinity College Dublin · IE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMacrophages play a pivotal role in atherosclerotic plaque development. Recent evidence has suggested the glucagon-like peptide-1 receptor (GLP-1R) agonist, liraglutide, can attenuate pro-inflammatory responses in macrophages. We hypothesized that liraglutide could limit atherosclerosis progression in vivo via modulation of the inflammatory response.

methodsHuman THP-1 macrophages and bone marrow-derived macrophages, from both wild-type C57BL/6 (WT) and apolipoprotein E null mice (ApoE

resultsLiraglutide decreased atherosclerotic lesion formation in ApoE

conclusionsThis data supports a therapeutic role for liraglutide as an atheroprotective agent via modulating macrophage cell fate towards MΦ2 pro-resolving macrophages.

Indexed as

PhenotypeAnimalsApolipoproteins EAtherosclerosisCell LineHumansHypoglycemic AgentsLeukocytes, MononuclearLiraglutideMacrophagesMiceMice, Inbred C57BLMice, KnockoutApolipoproteins EHypoglycemic AgentsLiraglutideAnti-inflammatoryAtherosclerosisMonocytesMΦ2 macrophagesPlaque microenvironment

Identifiers

PMID29110715
PMCPMC5674826
OpenAlexW2767936163

What OpenQuestion holds

Textfull text, public
LicenceCC BY
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.