Evidence map›Paper›PMID 19920044›Full record

ArticleCirculation. Cardiovascular imaging2009

Molecular MRI of cardiomyocyte apoptosis with simultaneous delayed-enhancement MRI distinguishes apoptotic and necrotic myocytes in vivo: potential for midmyocardial salvage in acute ischemia.

David E Sosnovik, Elisabeth Garanger, Elena Aikawa, Matthias Nahrendorf, Jose-Luiz Figuiredo, Guangping Dai, Fred Reynolds, Anthony Rosenzweig, Ralph Weissleder, Lee Josephson

Abstract read
In one paragraph

Article in Circulation. Cardiovascular imaging, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 46 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
46citing papers in PubMed, 1 pooled it
–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

46 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Guidelines for measuring cardiac physiology in mice.American journal of physiology. Heart and circulatory physiology · 2018
    Guideline
  2. Article
  3. Article
  4. Review
  5. Review
  6. Article
  7. Molecular Imaging of the Heart.Comprehensive Physiology · 2019
    Review
  8. Review
  9. Molecular Imaging in Ischemic Heart Disease.Current cardiovascular imaging reports · 2019
    Review
  10. Article
  11. Review
  12. Review
  13. Article
  14. Multimodality imaging demonstrates trafficking of liposomes preferentially to ischemic myocardium.Cardiovascular revascularization medicine : including molecular interventions · 2016
    Article
  15. Article
  16. Review
  17. Imaging of early modification in cardiomyopathy: the doxorubicin-induced model.The international journal of cardiovascular imaging · 2013
    Review
  18. Review
  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

10 authors.

David E SosnovikCenter for Molecular Imaging Research, the Cardiology Division, Martinos Center for Biomedical Imaging, and the Center for Systems Biology, Massachusetts General Hospital, Harvard Medical School, Boston. Mass, USA. sosnovik@nmr.mgh.harvard.edu
Elisabeth Garanger
Elena Aikawa
Matthias Nahrendorf
Jose-Luiz Figuiredo
Guangping Dai
Fred Reynolds
Anthony Rosenzweig
Ralph Weissleder
Lee Josephson

Funding

StatisticsP50CA086355 · NCI · MASSACHUSETTS GENERAL HOSPITAL · PI WEISSLEDER, MD, PHD, RALPH · 2000 to 2015
$27.8M
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
Small Animal Imaging ResourceU24CA092782 · NCI · MASSACHUSETTS GENERAL HOSPITAL · PI NAHRENDORF, MATTHIAS, WEISSLEDER, MD, PHD, RALPH · 2007 to 2011
$2.7M
Molecular and Microstructural Imaging of Cardiomyocyte Apoptosis and AutophagyR01HL093038 · NHLBI · MASSACHUSETTS GENERAL HOSPITAL · PI SOSNOVIK, DAVID E · 2008 to 2012
$2.2M
Reagents for the Design of Targeted Multifunctional NanomaterialsR01EB009691 · NIBIB · MASSACHUSETTS GENERAL HOSPITAL · PI JOSEPHSON, LEE · 2009 to 2012
$1.5M
Imaging of Pharmacotherapy Induced ApoptosisR01EB004472 · NIBIB · MASSACHUSETTS GENERAL HOSPITAL · PI JOSEPHSON, LEE · 2005 to 2008
$1.5M
MR imaging of myeloperoxidase activityR01HL078641 · NHLBI · MASSACHUSETTS GENERAL HOSPITAL · PI WEISSLEDER, RALPH · 2004 to 2007
$1.5M
Magnetic Resonance Imaging of Cardiomyocyte ApoptosisK08HL079984 · NHLBI · MASSACHUSETTS GENERAL HOSPITAL · PI SOSNOVIK, DAVID E · 2005 to 2009
$661k
NCI NIH HHS CA-86355NCI NIH HHS CA-92782NCI NIH HHS P50 CA086355NCI NIH HHS R24 CA092782NCI NIH HHS U24 CA092782NHLBI NIH HHS HL-078641NHLBI NIH HHS HL-080731NHLBI NIH HHS K08 HL079984NHLBI NIH HHS K08-HL079984NHLBI NIH HHS R01 HL078641NHLBI NIH HHS R01 HL093038NHLBI NIH HHS R01-HL093038NHLBI NIH HHS U01 HL080731NIBIB NIH HHS R01 EB004472NIBIB NIH HHS R01EB004472NIBIB NIH HHS R01 EB009691
6 · The paper itself

Abstract

backgroundA novel dual-contrast molecular MRI technique to image both cardiomyocyte apoptosis and necrosis in vivo within 4 to 6 hours of ischemia is presented. The technique uses the annexin-based nanoparticle AnxCLIO-Cy5.5 (apoptosis) and simultaneous delayed-enhancement imaging with a novel gadolinium chelate, Gd-DTPA-NBD (necrosis). METHODS AND

resultsMice with transient coronary ligation were injected intravenously at the onset of reperfusion with AnxCLIO-Cy5.5 (n=7) or the control probe Inact_CLIO-Cy5.5 (n=6). T2*-weighted MR images (9.4 T) were acquired within 4 to 6 hours of reperfusion. The contrast-to-noise ratio between injured and uninjured myocardium was measured. The mice were then injected with Gd-DTPA-NBD, and delayed-enhancement imaging was performed within 10 to 30 minutes. Uptake of AnxCLIO-Cy5.5 was most prominent in the midmyocardium and was significantly greater than that of Inact_CLIO-Cy5.5 (contrast-to-noise ratio, 8.82+/-1.5 versus 3.78+/-1.1; P<0.05). Only 21+/-3% of the myocardium with accumulation of AnxCLIO-Cy5.5 showed delayed-enhancement of Gd-DTPA-NBD. Wall thickening was significantly reduced in segments with delayed enhancement and/or transmural accumulation of AnxCLIO-Cy5.5 (P<0.001). Fluorescence microscopy of AnxCLIO-Cy5.5 and immunohistochemistry of Gd-DTPA-NBD confirmed the presence of large numbers of apoptotic but potentially viable cardiomyocytes (AnxCLIO-Cy5.5 positive, Gd-DTPA-NBD negative) in the midmyocardium.

conclusionsA novel technique to image cardiomyocyte apoptosis and necrosis in vivo within 4 to 6 hours of injury is presented and reveals large areas of apoptotic but viable myocardium in the midmyocardium. Strategies to salvage the numerous apoptotic but potentially viable cardiomyocytes in the midmyocardium in acute ischemia should be investigated.

Indexed as

ApoptosisNanoparticles4-Chloro-7-nitrobenzofurazanAnalysis of VarianceAnimalsAnnexin A5AnnexinsCarbocyaninesContrast MediaFlow CytometryGadolinium DTPAImage Processing, Computer-AssistedIn Situ Nick-End LabelingMagnetic Resonance ImagingMiceMice, Inbred C57BL4-Chloro-7-nitrobenzofurazanAnnexin A5AnnexinsCarbocyaninesContrast MediaCY5.5 cyanine dyeGadolinium DTPAOrganometallic CompoundsPentetic Acid

Identifiers

PMID19920044
PMCPMC2780438

What OpenQuestion holds

Textmetadata
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.