Evidence map›Paper›PMID 24893977›Full record

ArticleJournal of visualized experiments : JoVE2014

Inducing myointimal hyperplasia versus atherosclerosis in mice: an introduction of two valid models.

Mandy Stubbendorff, Xiaoqin Hua, Tobias Deuse, Ziad Ali, Hermann Reichenspurner, Lars Maegdefessel, Robert C Robbins, Sonja Schrepfer

Open access · bronzeAbstract readVideo-Audio Media
In one paragraph

Article in Journal of visualized experiments : JoVE, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.2field-weighted citation impact, top 40% 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

5 citing papers in PubMed, 8 citations in OpenAlex.

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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

8 authors at 5 institutions in 4 countries.

Mandy StubbendorffTransplant and Stem Cell Immunobiology Lab, Cardiovascular Research Center, University Hospital Hamburg; Cardiovascular Research Center (CVRC) and DZHK University Hamburg.
Xiaoqin HuaTransplant and Stem Cell Immunobiology Lab, Cardiovascular Research Center, University Hospital Hamburg; Cardiovascular Research Center (CVRC) and DZHK University Hamburg.
Tobias DeuseTransplant and Stem Cell Immunobiology Lab, Cardiovascular Research Center, University Hospital Hamburg; Cardiovascular Research Center (CVRC) and DZHK University Hamburg; Department of Cardiovascular Surgery, University Heart Center Hamburg.
Ziad AliCenter for Interventional Vascular Therapy, Division of Cardiology, Columbia University; Cardiovascular Research Foundation, New York.
Hermann ReichenspurnerCardiovascular Research Center (CVRC) and DZHK University Hamburg; Department of Cardiovascular Surgery, University Heart Center Hamburg.
Lars MaegdefesselKarolinska Institute, Stockholm.
Robert C RobbinsDepartment of Cardiothoracic Surgery, Stanford University School of Medicine, Falk Cardiovascular Research Center.
Sonja SchrepferTransplant and Stem Cell Immunobiology Lab, Cardiovascular Research Center, University Hospital Hamburg; Cardiovascular Research Center (CVRC) and DZHK University Hamburg; Department of Cardiovascular Surgery, University Heart Center Hamburg; Center for Interventional Vascular Therapy, Division of Cardiology, Columbia University; schrepfer@stanford.edu.
Cardiovascular Research Center · BRUniversität Hamburg · DEUniversity Medical Center Hamburg-Eppendorf · DEColumbia University · USKarolinska Institutet · SE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Various in vivo laboratory rodent models for the induction of artery stenosis have been established to mimic diseases that include arterial plaque formation and stenosis, as observed for example in ischemic heart disease. Two highly reproducible mouse models - both resulting in artery stenosis but each underlying a different pathway of development - are introduced here. The models represent the two most common causes of artery stenosis; namely one mouse model for each myointimal hyperplasia, and atherosclerosis are shown. To induce myointimal hyperplasia, a balloon catheter injury of the abdominal aorta is performed. For the development of atherosclerotic plaque, the ApoE -/- mouse model in combination with western fatty diet is used. Different model-adapted options for the measurement and evaluation of the results are named and described in this manuscript. The introduction and comparison of these two models provides information for scientists to choose the appropriate artery stenosis model in accordance to the scientific question asked.

Indexed as

Disease Models, AnimalAnimalsApolipoproteins EAtherosclerosisFemaleHyperplasiaMaleMiceMice, Inbred C57BLPlaque, AtheroscleroticReproducibility of ResultsTunica IntimaApolipoproteins E

Identifiers

PMID24893977
PMCPMC4186352
OpenAlexW2086685293

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.