Evidence map›Paper›PMID 26206580›Full record

Observational studyJournal of vascular surgery2015

Distinct macrophage phenotype and collagen organization within the intraluminal thrombus of abdominal aortic aneurysm.

Jayashree Rao, Bryan N Brown, Justin S Weinbaum, Emily L Ofstun, Michel S Makaroun, Jay D Humphrey, David A Vorp

Open access · bronzeAbstract readObservational Study
In one paragraph

Observational study in Journal of vascular surgery, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
1.7field-weighted citation impact, top 15% 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, 33 citations in OpenAlex.

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  5. NanoSHP099-Targeted SHP2 Inhibition Boosts Ly6CAdvanced science (Weinheim, Baden-Wurttemberg, Germany) · 2024
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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

7 authors at 2 institutions in 1 country.

Jayashree RaoDepartment of Bioengineering, University of Pittsburgh, Pittsburgh, Pa.
Bryan N BrownDepartment of Bioengineering, McGowan Institute for Regenerative Medicine, University of Pittsburgh, Pittsburgh, Pa.
Justin S WeinbaumDepartment of Bioengineering, and McGowan Institute for Regenerative Medicine, University of Pittsburgh, Pittsburgh, Pa.
Emily L OfstunDepartment of Bioengineering, University of Pittsburgh, Pittsburgh, Pa.
Michel S MakarounDepartment of Surgery, Division of Vascular Surgery, Center for Vascular Remodeling and Regeneration, University of Pittsburgh, Pittsburgh, Pa.
Jay D HumphreyDepartment of Biomedical Engineering, Yale University, New Haven, Conn.
David A VorpDepartment of Bioengineering, Department of Cardiothoracic Surgery, Department of Surgery, Center for Vascular Remodeling and Regeneration, McGowan Institute for Regenerative Medicine, University of Pittsburgh, Pittsburgh, Pa. Electronic address: vorp@pitt.edu.
University of Pittsburgh · USYale University · US

Funding

Biomechanical Simulation of Evolving Aortic Aneurysms for Designing InterventionR01HL086418 · NHLBI · YALE UNIVERSITY · PI HUMPHREY, JAY D. · 2008 to 2017
$3.8M
NHLBI NIH HHS HL-086418NHLBI NIH HHS R01 HL086418
6 · The paper itself

Abstract

objectiveLittle is known about the etiologic factors that lead to the occurrence of intraluminal thrombus (ILT) during abdominal aortic aneurysm (AAA) development. Recent work has suggested that macrophages may play an important role in progression of a number of other vascular diseases, including atherosclerosis; however, whether these cells are present within the ILT of a progressing AAA is unknown. The purpose of this work was to define the presence, phenotype, and spatial distribution of macrophages within the ILT excised from six patients. We hypothesized that the ILT contains a population of activated macrophages with a distinct, nonclassical phenotypic profile.

methodsILT samples were examined using histologic staining and immunofluorescent labeling for multiple markers of activated macrophages (cluster of differentiation [CD]45, CD68, human leukocyte antigen-DR, matrix metalloproteinase 9) and the additional markers α-smooth muscle actin, CD34, CD105, fetal liver kinase-1, and collagen I and III.

resultsHistologic staining revealed a distinct laminar organization of collagen within the shoulder region of the ILT lumen and a spatially heterogeneous cell composition within the ILT. Most of the cellular constituents of the ILT were in the luminal region and predominantly expressed markers of activated macrophages but also concurrently expressed α-smooth muscle actin, CD105, and synthesized collagen I and III.

conclusionsThis report presents evidence for the presence of a distinct macrophage population within the luminal region of AAA ILT. These cells express a set of markers indicative of a unique population of activated macrophages. The exact contributions of these previously unrecognized cells to ILT formation and AAA pathobiology remains unknown.

Indexed as

AgedAorta, AbdominalAortic Aneurysm, AbdominalBiomarkersCollagenFemaleHumansMacrophage ActivationMacrophagesMalePhenotypeThrombosisBiomarkersCollagen

Identifiers

PMID26206580
PMCPMC4550501
OpenAlexW2158471444

What OpenQuestion holds

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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.