Evidence mapPaperPMID 39441910Full record

ReviewArteriosclerosis, thrombosis, and vascular biology2024

What Is the Best Experimental Model for Developing Novel Therapeutics in Peripheral Artery Disease?

Anne Lejay, Winona W Wu, Salomé H Kuntz, Mark W Feinberg

Abstract readReview
In one paragraph

Review in Arteriosclerosis, thrombosis, and vascular biology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
field-weighted citation impact
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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. 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

4 authors.

Anne Lejay *Department of Vascular Surgery and Kidney Transplantation, University Hospital of Strasbourg, France (A.L., S.H.K.).ORCID 0000-0002-1041-0893
Winona W Wu *Cardiovascular Division, Department of Medicine, Brigham and Women's Hospital (W.W.W., M.W.F.), Harvard Medical School, Boston, MA.
Salomé H KuntzDepartment of Vascular Surgery and Kidney Transplantation, University Hospital of Strasbourg, France (A.L., S.H.K.).ORCID 0000-0002-3350-2264
Mark W FeinbergCardiovascular Division, Department of Medicine, Brigham and Women's Hospital (W.W.W., M.W.F.), Harvard Medical School, Boston, MA.ORCID 0000-0001-9523-3859

Funding

HARVARD-LONGWOOD RESEARCH TRAINING IN VASCULAR SURGERYT32HL007734 · BETH ISRAEL DEACONESS MEDICAL CENTER · 1993 to 2005
$1.7M
miR-130b, angiogenesis, and diabetic critical limb ischemiaR01HL167905 · BRIGHAM AND WOMEN'S HOSPITAL · 2025 to 2025
$660k
NHLBI NIH HHS R01 HL115141NHLBI NIH HHS R01 HL148207NHLBI NIH HHS R01 HL148355NHLBI NIH HHS R01 HL153356NHLBI NIH HHS R01 HL167905NHLBI NIH HHS T32 HL007734
6 · The paper itself

Abstract

clinical problemMore than 200 million people worldwide have peripheral artery disease (PAD). PAD affects the quality of life and is associated with significant morbidity and mortality. Standard treatment for severe cases of PAD is surgical or endovascular revascularization. However, up to 30% of patients are not candidates for open or endovascular procedures, due to high operative risk or unfavorable vascular involvement. Furthermore, revascularization procedures may be insufficient to adequately improve microvascular tissue perfusion, wound healing, or limb salvage. Accordingly, regardless of advances in treatment modalities, outcomes of patients with PAD have remained unfavorable. Therefore, new medical therapeutic approaches are much needed. Small animal models are indispensable tools for the understanding of PAD physiopathology and the development of novel medical therapies. RECOMMENDATIONS FOR INCREASING TRANSLATION FROM ANIMAL MODELS: Development of animal models that more closely mimic the pathophysiology (with occlusive atherothrombosis and chronic development of limb ischemia) can incorporate the cardiovascular risk factors associated with this disease state, and focus on more clinically relevant outcomes is critical. In practice, this means using both animals that develop atherosclerosis and methods for the application of gradual arterial occlusion to induce hind limb ischemia. Doing so will likely help identify novel targets for intervention and overcome some principal challenges confronted by previous clinical trials. While various rodent models are discussed, the optimal animal model is yet to be defined.

Indexed as

Disease Models, AnimalPeripheral Arterial DiseaseAnimalsHumansheart disease risk factorsmodels, animalmorbiditythrombosiswound healing

Identifiers

PMID39441910
PMCPMC11501046

What Socratic holds

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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 Socratic graph.