Evidence map›Paper›PMID 29186427›Full record

ArticleEndocrinology2018

Insulinlike Growth Factor-Binding Protein-1 Improves Vascular Endothelial Repair in Male Mice in the Setting of Insulin Resistance.

Amir Aziz, Natalie J Haywood, Paul A Cordell, Jess Smith, Nadira Y Yuldasheva, Anshuman Sengupta, Noman Ali, Ben N Mercer, Romana S Mughal, Kirsten Riches and 4 more

Open access · bronzeAbstract read
In one paragraph

Article in Endocrinology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
0.6field-weighted citation impact, top 33% 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

13 citing papers in PubMed, 15 citations in OpenAlex.

  1. Observational
  2. Article
  3. Article
  4. Review
  5. Impaired Angiogenic Function of Fetal Endothelial Progenitor Cells viaInternational journal of molecular sciences · 2023
    Article
  6. Article
  7. Plasma human growth cytokines in children with vasovagal syncope.Frontiers in cardiovascular medicine · 2022
    Article
  8. Article
  9. Review
  10. Protein Biomarkers and Risk of Atrial Fibrillation: The FHS.Circulation. Arrhythmia and electrophysiology · 2020
    Article
  11. Article
  12. Article
  13. Article
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

14 authors at 2 institutions in 1 country.

Amir AzizLeeds Institute of Cardiovascular and Metabolic Medicine and Multidisciplinary Cardiovascular Research Centre, University of Leeds, Leeds, United Kingdom.
Natalie J HaywoodLeeds Institute of Cardiovascular and Metabolic Medicine and Multidisciplinary Cardiovascular Research Centre, University of Leeds, Leeds, United Kingdom.
Paul A CordellLeeds Institute of Cardiovascular and Metabolic Medicine and Multidisciplinary Cardiovascular Research Centre, University of Leeds, Leeds, United Kingdom.
Jess SmithLeeds Institute of Cardiovascular and Metabolic Medicine and Multidisciplinary Cardiovascular Research Centre, University of Leeds, Leeds, United Kingdom.
Nadira Y YuldashevaLeeds Institute of Cardiovascular and Metabolic Medicine and Multidisciplinary Cardiovascular Research Centre, University of Leeds, Leeds, United Kingdom.
Anshuman SenguptaLeeds Institute of Cardiovascular and Metabolic Medicine and Multidisciplinary Cardiovascular Research Centre, University of Leeds, Leeds, United Kingdom.
Noman AliLeeds Institute of Cardiovascular and Metabolic Medicine and Multidisciplinary Cardiovascular Research Centre, University of Leeds, Leeds, United Kingdom.
Ben N MercerLeeds Institute of Cardiovascular and Metabolic Medicine and Multidisciplinary Cardiovascular Research Centre, University of Leeds, Leeds, United Kingdom.
Romana S MughalLeeds Institute of Cardiovascular and Metabolic Medicine and Multidisciplinary Cardiovascular Research Centre, University of Leeds, Leeds, United Kingdom.
Kirsten RichesSchool of Chemistry and Biosciences, University of Bradford, Bradford, United Kingdom.
Richard M CubbonLeeds Institute of Cardiovascular and Metabolic Medicine and Multidisciplinary Cardiovascular Research Centre, University of Leeds, Leeds, United Kingdom.
Karen E PorterLeeds Institute of Cardiovascular and Metabolic Medicine and Multidisciplinary Cardiovascular Research Centre, University of Leeds, Leeds, United Kingdom.
Mark T KearneyLeeds Institute of Cardiovascular and Metabolic Medicine and Multidisciplinary Cardiovascular Research Centre, University of Leeds, Leeds, United Kingdom.
Stephen B WheatcroftLeeds Institute of Cardiovascular and Metabolic Medicine and Multidisciplinary Cardiovascular Research Centre, University of Leeds, Leeds, United Kingdom.
University of Leeds · GBUniversity of Bradford · GB

Funding

British Heart Foundation CH/13/1/30086British Heart Foundation FS/11/44/28820British Heart Foundation FS/11/73/29014British Heart Foundation FS/11/94/29180British Heart Foundation FS/12/51/29584British Heart Foundation FS/12/80/29821British Heart Foundation RG/15/7/31521
6 · The paper itself

Abstract

Insulin resistance is associated with impaired endothelial regeneration in response to mechanical injury. We recently demonstrated that insulinlike growth factor-binding protein-1 (IGFBP1) ameliorated insulin resistance and increased nitric oxide generation in the endothelium. In this study, we hypothesized that IGFBP1 would improve endothelial regeneration and restore endothelial reparative functions in the setting of insulin resistance. In male mice heterozygous for deletion of insulin receptors, endothelial regeneration after femoral artery wire injury was enhanced by transgenic expression of human IGFBP1 (hIGFBP1). This was not explained by altered abundance of circulating myeloid angiogenic cells. Incubation of human endothelial cells with hIGFBP1 increased integrin expression and enhanced their ability to adhere to and repopulate denuded human saphenous vein ex vivo. In vitro, induction of insulin resistance by tumor necrosis factor α (TNFα) significantly inhibited endothelial cell migration and proliferation. Coincubation with hIGFBP1 restored endothelial migratory and proliferative capacity. At the molecular level, hIGFBP1 induced phosphorylation of focal adhesion kinase, activated RhoA and modulated TNFα-induced actin fiber anisotropy. Collectively, the effects of hIGFBP1 on endothelial cell responses and acceleration of endothelial regeneration in mice indicate that manipulating IGFBP1 could be exploited as a putative strategy to improve endothelial repair in the setting of insulin resistance.

Indexed as

Insulin ResistanceAnimalsCell MovementEndothelial CellsEndothelium, VascularFemaleFocal Adhesion Protein-Tyrosine KinasesHumansInsulin-Like Growth Factor Binding Protein 1IntegrinsMaleMiceMice, Inbred C57BLMice, TransgenicPhosphorylationTumor Necrosis Factor-alphaFocal Adhesion Protein-Tyrosine KinasesInsulin-Like Growth Factor Binding Protein 1IntegrinsTumor Necrosis Factor-alpha

Identifiers

PMID29186427
PMCPMC5776633
OpenAlexW2768956134

What OpenQuestion holds

Textmetadata
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.