Evidence map›Paper›PMID 31069401›Full record

ArticleDiabetologia2019

ApoAI-derived peptide increases glucose tolerance and prevents formation of atherosclerosis in mice.

Shelley J Edmunds, Rebeca Liébana-García, Oktawia Nilsson, Joan Domingo-Espín, Caitriona Grönberg, Karin G Stenkula, Jens O Lagerstedt

Open access · hybridAbstract read
In one paragraph

Article in Diabetologia, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
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.

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

14 citing papers in PubMed, 25 citations in OpenAlex.

  1. Article
  2. Review
  3. New Player in an Old Field? Ecto-FArteriosclerosis, thrombosis, and vascular biology · 2024
    Article
  4. Article
  5. Article
  6. Review
  7. Review
  8. Review
  9. HDL Cholesterol and Non-Cardiovascular Disease: A Narrative Review.International journal of molecular sciences · 2021
    Review
  10. Review
  11. APOA1: a Protein with Multiple Therapeutic Functions.Current atherosclerosis reports · 2021
    Review
  12. Article
  13. Article
  14. Review
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 1 institution in 1 country.

Shelley J EdmundsDepartment of Experimental Medical Science, Biomedical Center Floor C13, Lund University, Tornavagen 10, 221 84, Lund, Sweden.
Rebeca Liébana-GarcíaDepartment of Experimental Medical Science, Biomedical Center Floor C13, Lund University, Tornavagen 10, 221 84, Lund, Sweden.
Oktawia NilssonDepartment of Experimental Medical Science, Biomedical Center Floor C13, Lund University, Tornavagen 10, 221 84, Lund, Sweden.
Joan Domingo-EspínDepartment of Experimental Medical Science, Biomedical Center Floor C13, Lund University, Tornavagen 10, 221 84, Lund, Sweden.
Caitriona GrönbergDepartment of Experimental Medical Science, Biomedical Center Floor C13, Lund University, Tornavagen 10, 221 84, Lund, Sweden.
Karin G StenkulaDepartment of Experimental Medical Science, Biomedical Center Floor C13, Lund University, Tornavagen 10, 221 84, Lund, Sweden.
Jens O LagerstedtDepartment of Experimental Medical Science, Biomedical Center Floor C13, Lund University, Tornavagen 10, 221 84, Lund, Sweden. jens.lagerstedt@med.lu.se.
Lund University · SE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aims/hypothesisFinding new treatment alternatives for individuals with diabetes with severe insulin resistance is highly desired. To identify novel mechanisms that improve glucose uptake in skeletal muscle, independently from insulin levels and signalling, we have explored the therapeutic potential of a short peptide sequence, RG54, derived from apolipoprotein A-I (ApoA-I).

methodsINS-1E rat clonal beta cells, C2C12 rat muscle myotubes and J774 mouse macrophages were used to study the impact of RG54 peptide on glucose-stimulated insulin secretion, glucose uptake and cholesterol efflux, respectively. GTTs were carried out on diet-induced insulin-resistant and Lepr

resultsThe synthetic RG54 peptide induced glucose uptake in cultured muscle myotubes by a similar amount as insulin, and also primed pancreatic beta cells for improved glucose-stimulated insulin secretion. The findings were verified in diet-induced insulin-resistant and Lepr CONCLUSIONS/

interpretationThe RG54 peptide exhibits good prospects for providing glucose control and reducing the risk of cardiovascular disease in individuals with severe insulin resistance.

Indexed as

AnimalsApolipoprotein A-IAtherosclerosisBlood GlucoseDiabetes Mellitus, ExperimentalDiabetes Mellitus, Type 2GlucoseInsulin ResistanceMaleMiceMice, Inbred C57BLPeptidesApolipoprotein A-IBlood GlucoseGlucosePeptidesApoA-IAtherosclerosisCardiovascular diseaseDiabetesGlucose tolerance testGlycaemic controlHDLInsulinPeptideRG54

Identifiers

PMID31069401
PMCPMC6560211
OpenAlexW2943899390

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.