Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
2
pubmed:dateCreated
2008-2-4
pubmed:abstractText
Acute myocardial infarction (AMI) research relies increasingly on small animal models and noninvasive imaging methods such as MRI, single-photon emission computed tomography (SPECT), and positron emission tomography (PET). However, a direct comparison among these techniques for characterization of perfusion, viability, and infarct size is lacking. Rats were studied within 18-24 hr post AMI by MRI (4.7 T) and subsequently (40-48 hr post AMI) by SPECT ((99)Tc-MIBI) and micro-PET ((18)FDG). A necrosis-specific MRI contrast agent was used to detect AMI, and a fast low angle shot (FLASH) sequence was used to acquire late enhancement and functional images contemporaneously. Infarcted regions showed late enhancement, whereas corresponding radionuclide images had reduced tracer uptake. MRI most accurately depicted AMI, showing the closest correlation and agreement with triphenyl tetrazolium chloride (TTC), followed by SPECT and PET. In some animals a mismatch of reduced uptake in normal myocardium and relatively increased (18)FDG uptake in the infarct border zone precluded conventional quantitative analysis. We performed the first quantitative comparison of MRI, PET, and SPECT for reperfused AMI imaging in a small animal model. MRI was superior to the other modalities, due to its greater spatial resolution and ability to detect necrotic myocardium directly. The observed (18)FDG mismatch likely represents variable metabolic conditions between stunned myocardium in the infarct border zone and normal myocardium and supports the use of a standardized glucose load or glucose clamp technique for PET imaging of reperfused AMI in small animals.
pubmed:grant
pubmed:commentsCorrections
http://linkedlifedata.com/resource/pubmed/commentcorrection/18228591-10540668, http://linkedlifedata.com/resource/pubmed/commentcorrection/18228591-10556226, http://linkedlifedata.com/resource/pubmed/commentcorrection/18228591-10694532, http://linkedlifedata.com/resource/pubmed/commentcorrection/18228591-11733404, http://linkedlifedata.com/resource/pubmed/commentcorrection/18228591-11747006, http://linkedlifedata.com/resource/pubmed/commentcorrection/18228591-11955861, http://linkedlifedata.com/resource/pubmed/commentcorrection/18228591-12019905, http://linkedlifedata.com/resource/pubmed/commentcorrection/18228591-12062364, http://linkedlifedata.com/resource/pubmed/commentcorrection/18228591-12093780, http://linkedlifedata.com/resource/pubmed/commentcorrection/18228591-12097466, http://linkedlifedata.com/resource/pubmed/commentcorrection/18228591-12652548, http://linkedlifedata.com/resource/pubmed/commentcorrection/18228591-12906991, http://linkedlifedata.com/resource/pubmed/commentcorrection/18228591-12946475, http://linkedlifedata.com/resource/pubmed/commentcorrection/18228591-1452936, http://linkedlifedata.com/resource/pubmed/commentcorrection/18228591-14530482, http://linkedlifedata.com/resource/pubmed/commentcorrection/18228591-14967719, http://linkedlifedata.com/resource/pubmed/commentcorrection/18228591-15302807, http://linkedlifedata.com/resource/pubmed/commentcorrection/18228591-15364813, http://linkedlifedata.com/resource/pubmed/commentcorrection/18228591-15534064, http://linkedlifedata.com/resource/pubmed/commentcorrection/18228591-15872356, http://linkedlifedata.com/resource/pubmed/commentcorrection/18228591-15937312, http://linkedlifedata.com/resource/pubmed/commentcorrection/18228591-16518671, http://linkedlifedata.com/resource/pubmed/commentcorrection/18228591-16669177, http://linkedlifedata.com/resource/pubmed/commentcorrection/18228591-17079817, http://linkedlifedata.com/resource/pubmed/commentcorrection/18228591-17268027, http://linkedlifedata.com/resource/pubmed/commentcorrection/18228591-7522135, http://linkedlifedata.com/resource/pubmed/commentcorrection/18228591-7678396, http://linkedlifedata.com/resource/pubmed/commentcorrection/18228591-9124430
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Feb
pubmed:issn
0740-3194
pubmed:author
pubmed:copyrightInfo
(c) 2008 Wiley-Liss, Inc.
pubmed:issnType
Print
pubmed:volume
59
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
252-9
pubmed:dateRevised
2010-9-21
pubmed:meshHeading
pubmed-meshheading:18228591-Animals, pubmed-meshheading:18228591-Contrast Media, pubmed-meshheading:18228591-Disease Models, Animal, pubmed-meshheading:18228591-Fluorodeoxyglucose F18, pubmed-meshheading:18228591-Gadolinium DTPA, pubmed-meshheading:18228591-Image Processing, Computer-Assisted, pubmed-meshheading:18228591-Magnetic Resonance Imaging, pubmed-meshheading:18228591-Male, pubmed-meshheading:18228591-Metalloporphyrins, pubmed-meshheading:18228591-Myocardial Infarction, pubmed-meshheading:18228591-Positron-Emission Tomography, pubmed-meshheading:18228591-Radiopharmaceuticals, pubmed-meshheading:18228591-Rats, pubmed-meshheading:18228591-Rats, Sprague-Dawley, pubmed-meshheading:18228591-Staining and Labeling, pubmed-meshheading:18228591-Technetium Tc 99m Sestamibi, pubmed-meshheading:18228591-Tomography, Emission-Computed, Single-Photon
pubmed:year
2008
pubmed:articleTitle
Noninvasive assessment of myocardial viability in a small animal model: comparison of MRI, SPECT, and PET.
pubmed:affiliation
Department of Radiology, University of Pennsylvania, 3400 Spruce Street, Philadelphia, PA 19104, USA.
pubmed:publicationType
Journal Article, Comparative Study, Research Support, Non-U.S. Gov't, Research Support, N.I.H., Extramural