Evidence map›Paper›PMID 19833312›Full record

ArticleJACC. Cardiovascular imaging2009

18F-4V for PET-CT imaging of VCAM-1 expression in atherosclerosis.

Matthias Nahrendorf, Edmund Keliher, Peter Panizzi, Hanwen Zhang, Sheena Hembrador, Jose-Luiz Figueiredo, Elena Aikawa, Kimberly Kelly, Peter Libby, Ralph Weissleder

Open access · greenAbstract readValidation StudyComment
In one paragraph

Article in JACC. Cardiovascular imaging, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 94 papers.

0numbers the graph read from it
0cells of the map it votes in
94citing papers in PubMed
9.4field-weighted citation impact, top 1% 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

94 citing papers in PubMed, 218 citations in OpenAlex.

  1. From incidental positron emission uptake toFrontiers in cardiovascular medicine · 2026
    Review
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  6. An Overview of In Vitro Assays ofDiagnostics (Basel, Switzerland) · 2023
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  12. Article
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  14. Inflammatory Cell Recruitment in Cardiovascular Disease.Frontiers in cell and developmental biology · 2021
    Review
  15. Review
  16. Review
  17. Review
  18. Selective targeting of nanomedicine to inflamed cerebral vasculature to enhance the blood-brain barrier.Proceedings of the National Academy of Sciences of the United States of America · 2020
    Article
  19. Current medicinal chemistry · 2020
    Review
  20. Article

34 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors at 2 institutions in 1 country.

Matthias NahrendorfCenter for Systems Biology, Massachusetts General Hospital and Harvard Medical School, Boston, Massachusetts 02124, USA.
Edmund Keliher
Peter Panizzi
Hanwen Zhang
Sheena Hembrador
Jose-Luiz Figueiredo
Elena Aikawa
Kimberly Kelly
Peter Libby
Ralph Weissleder
Harvard University · USBrigham and Women's Hospital · US

Funding

Translational Program of Excellence in NanotechnologyU01HL080731 · NHLBI · MASSACHUSETTS GENERAL HOSPITAL · PI WEISSLEDER, MD, PHD, RALPH · 2005 to 2009
$14.9M
Small Animal Imaging Resource GrantR24CA092782 · NCI · MASSACHUSETTS GENERAL HOSPITAL · PI WEISSLEDER, RALPH · 2001 to 2006
$4.2M
Integrated FMT approaches for biomolecular measurementsR01EB006432 · NIBIB · MASSACHUSETTS GENERAL HOSPITAL · PI WEISSLEDER, MD, PHD, RALPH · 2006 to 2013
$3.0M
PET/MRI of cardiac repairR01HL096576 · NHLBI · MASSACHUSETTS GENERAL HOSPITAL · PI NAHRENDORF, MATTHIAS · 2009 to 2017
$2.8M
Imaging of Cardiac Transplant RejectionR01HL095629 · NHLBI · MASSACHUSETTS GENERAL HOSPITAL · PI NAHRENDORF, MATTHIAS · 2009 to 2013
$2.2M
MR imaging of myeloperoxidase activityR01HL078641 · NHLBI · MASSACHUSETTS GENERAL HOSPITAL · PI WEISSLEDER, RALPH · 2004 to 2007
$1.5M
Development of Molecularly Targeted Imaging Agents for Early Detection of PDACR01CA137071 · NCI · UNIVERSITY OF VIRGINIA · PI KELLY, KIMBERLY A. · 2008 to 2012
$1.3M
Pathobiology of Staphyloccocus areus EndocarditisR00HL094533 · NHLBI · AUBURN UNIVERSITY AT AUBURN · PI PANIZZI, PETER ROLF · 2011 to 2013
$719k
NCI NIH HHS R01 CA137071NCI NIH HHS R24 CA092782NCI NIH HHS R24-CA92782NHLBI NIH HHS R00 HL094533NHLBI NIH HHS R01 HL078641NHLBI NIH HHS R01-HL078641NHLBI NIH HHS R01 HL095629NHLBI NIH HHS R01 HL096576NHLBI NIH HHS U01 HL080731NHLBI NIH HHS UO1-HL080731NIBIB NIH HHS R01 EB006432
6 · The paper itself

Abstract

objectivesThe aim of this study was to iteratively develop and validate an (18)F-labeled small vascular cell adhesion molecule (VCAM)-1 affinity ligand and demonstrate the feasibility of imaging VCAM-1 expression by positron emission tomography-computed tomography (PET-CT) in murine atherosclerotic arteries.

backgroundHybrid PET-CT imaging allows simultaneous assessment of atherosclerotic lesion morphology (CT) and may facilitate early risk assessment in individual patients. The early induction, confinement of expression to atherosclerotic lesions, and accessible position in proximity to the blood pool render the adhesion molecule VCAM-1 an attractive imaging biomarker for inflamed atheroma prone to complication.

methodsA cyclic, a linear, and an oligomer affinity peptide, internalized into endothelial cells by VCAM-1-mediated binding, were initially derivatized with DOTA to determine their binding profiles and pharmacokinetics. The lead compound was then (18)F-labeled and tested in atherosclerotic apoE(-/-) mice receiving a high-cholesterol diet as well as wild type murine models of myocardial infarction and heart transplant rejection.

resultsThe tetrameric peptide had the highest affinity and specificity for VCAM-1 (97% inhibition with soluble VCAM-1 in vitro). In vivo PET-CT imaging using (18)F-4V showed 0.31 +/- 0.02 SUV in murine atheroma (ex vivo %IDGT 5.9 +/- 1.5). (18)F-4V uptake colocalized with atherosclerotic plaques on Oil Red O staining and correlated to mRNA levels of VCAM-1 measured by quantitative reverse transcription polymerase chain reaction (R = 0.79, p = 0.03). Atherosclerotic mice receiving an atorvastatin-enriched diet had significantly lower lesional uptake (p < 0.05). Furthermore, (18)F-4V imaging in myocardial ischemia after coronary ligation and in transplanted cardiac allografts undergoing rejection showed high in vivo PET signal in inflamed myocardium and good correlation with ex vivo measurement of VCAM-1 mRNA by quantitative polymerase chain reaction.

conclusions(18)F-4V allows noninvasive PET-CT imaging of VCAM-1 in inflammatory atherosclerosis, has the dynamic range to quantify treatment effects, and correlates with inflammatory gene expression.

Indexed as

Fluorodeoxyglucose F18PeptidesRadiopharmaceuticalsTomography, X-Ray ComputedAnimalsApolipoproteins EAtherosclerosisAtorvastatinBinding, CompetitiveCells, CulturedContrast MediaDisease Models, AnimalEndothelium, VascularFeasibility StudiesGraft RejectionHalf-LifeApolipoproteins EAtorvastatinContrast MediaFluorodeoxyglucose F18Heptanoic AcidsHydroxymethylglutaryl-CoA Reductase InhibitorsInflammation MediatorsIopamidolLigandsPeptidesPyrrolesRadiopharmaceuticalsRNA, MessengerVascular Cell Adhesion Molecule-1

Identifiers

PMID19833312
PMCPMC2773129
OpenAlexW41685348

What OpenQuestion holds

Texttitle and abstract
LicenceTDM
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.