Evidence map›Paper›PMID 32629616›Full record

ArticleiScience2020

Obstruction of Small Arterioles in Patients with Critical Limb Ischemia due to Partial Endothelial-to-Mesenchymal Transition.

Jacqueline Chevalier, Hao Yin, John-Michael Arpino, Caroline O'Neil, Zengxuan Nong, Kevin J Gilmore, Jason J Lee, Emma Prescott, Matthew Hewak, Charles L Rice and 4 more

Open access · goldAbstract read
In one paragraph

Article in iScience, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed, 1 pooled it
3.5field-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.

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

23 citing papers in PubMed, 1 synthesis or guideline pooled it, 31 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. ILK-Dependent Modulation of DPP4 Prevents Progression of Calcific Aortic Valve Disease.Arteriosclerosis, thrombosis, and vascular biology · 2026
    Article
  4. Article
  5. Article
  6. Article
  7. Intussusceptive angiogenesis-on-a-chip: Evidence for transluminal vascular bridging by endothelial delamination.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  8. Article
  9. Review
  10. Article
  11. Endothelial-to-Mesenchymal Transition in Cardiovascular Pathophysiology.International journal of molecular sciences · 2024
    Review
  12. Article
  13. Review
  14. Article
  15. Endothelial-to-Mesenchymal Transition: Potential Target of Doxorubicin-Induced Cardiotoxicity.American journal of cardiovascular drugs : drugs, devices, and other interventions · 2023
    Review
  16. Article
  17. Review
  18. Article
  19. Article
  20. 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 1 institution in 1 country.

Jacqueline ChevalierRobarts Research Institute, Schulich School of Medicine and Dentistry, Western University, London, Canada; Department of Medical Biophysics, Schulich School of Medicine and Dentistry, Western University, London, Canada.
Hao YinRobarts Research Institute, Schulich School of Medicine and Dentistry, Western University, London, Canada.
John-Michael ArpinoRobarts Research Institute, Schulich School of Medicine and Dentistry, Western University, London, Canada; Department of Medical Biophysics, Schulich School of Medicine and Dentistry, Western University, London, Canada.
Caroline O'NeilRobarts Research Institute, Schulich School of Medicine and Dentistry, Western University, London, Canada.
Zengxuan NongRobarts Research Institute, Schulich School of Medicine and Dentistry, Western University, London, Canada.
Kevin J GilmoreDepartment of Anatomy and Cell Biology, Schulich School of Medicine and Dentistry, Western University, London, Canada; School of Kinesiology, Faculty of Health Sciences, Western University, London, Canada.
Jason J LeeRobarts Research Institute, Schulich School of Medicine and Dentistry, Western University, London, Canada; Department of Medicine, Schulich School of Medicine and Dentistry, Western University, London, Canada; Department of Medical Biophysics, Schulich School of Medicine and Dentistry, Western University, London, Canada.
Emma PrescottRobarts Research Institute, Schulich School of Medicine and Dentistry, Western University, London, Canada; Department of Medical Biophysics, Schulich School of Medicine and Dentistry, Western University, London, Canada.
Matthew HewakDepartment of Anatomy and Cell Biology, Schulich School of Medicine and Dentistry, Western University, London, Canada.
Charles L RiceDepartment of Anatomy and Cell Biology, Schulich School of Medicine and Dentistry, Western University, London, Canada; School of Kinesiology, Faculty of Health Sciences, Western University, London, Canada.
Luc DuboisDepartment of Surgery, Schulich School of Medicine and Dentistry, Western University, London, Canada.
Adam H PowerDepartment of Surgery, Schulich School of Medicine and Dentistry, Western University, London, Canada.
Douglas W HamiltonDepartment of Anatomy and Cell Biology, Schulich School of Medicine and Dentistry, Western University, London, Canada.
J Geoffrey PickeringRobarts Research Institute, Schulich School of Medicine and Dentistry, Western University, London, Canada; Department of Medicine, Schulich School of Medicine and Dentistry, Western University, London, Canada; Department of Medical Biophysics, Schulich School of Medicine and Dentistry, Western University, London, Canada; Department of Biochemistry, Schulich School of Medicine and Dentistry, Western University, London, Canada. Electronic address: gpickering@robarts.ca.
Western University · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Critical limb ischemia (CLI) is a hazardous manifestation of atherosclerosis and treatment failure is common. Abnormalities in the arterioles might underlie this failure but the cellular pathobiology of microvessels in CLI is poorly understood. We analyzed 349 intramuscular arterioles in lower limb specimens from individuals with and without CLI. Arteriolar densities were 1.8-fold higher in CLI muscles. However, 33% of small (<20 μm) arterioles were stenotic and 9% were completely occluded. The lumens were closed by bulky, re-oriented endothelial cells expressing abundant N-cadherin that uniquely localized between adjacent and opposing endothelial cells. S100A4 and SNAIL1 were also expressed, supporting an endothelial-to-mesenchymal transition. SMAD2/3 was activated in occlusive endothelial cells and TGFβ1 was increased in the adjacent mural cells. These findings identify a microvascular closure process based on mesenchymal transitions in a hyper-TGFß environment that may, in part, explain the limited success of peripheral artery revascularization procedures.

Indexed as

Clinical FindingHuman SpecimenPathophysiology

Identifiers

PMID32629616
PMCPMC7322363
OpenAlexW3033547751

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.