23Na chemical shift imaging and Gd enhancement of myocardial edema.
Identifieur interne : 000351 ( PubMed/Curation ); précédent : 000350; suivant : 00035223Na chemical shift imaging and Gd enhancement of myocardial edema.
Auteurs : Eissa N E. Aguor [Pays-Bas] ; Cees W A. Van De Kolk ; Fatih Arslan ; Marcel G J. Nederhoff ; Pieter A F M. Doevendans ; Gerard Pasterkamp ; Gustav J. Strijkers ; Cees J A. Van EchteldSource :
- The international journal of cardiovascular imaging [ 1875-8312 ] ; 2013.
Descripteurs français
- KwdFr :
- Animaux, Composés organiques du phosphore, Composés organométalliques, Diagnostic différentiel, Facteurs temps, Imagerie par résonance magnétique, Infarctus du myocarde (anatomopathologie), Isotopes du sodium, Myocarde (anatomopathologie), Myocarde (métabolisme), Mâle, Oedème cardiaque (anatomopathologie), Oedème cardiaque (diagnostic), Oedème cardiaque (métabolisme), Perfusion, Produits de contraste, Rat Wistar, Rats, Spectroscopie par résonance magnétique, Techniques in vitro, Valeur prédictive des tests.
- MESH :
- anatomopathologie : Infarctus du myocarde, Myocarde, Oedème cardiaque.
- diagnostic : Oedème cardiaque.
- métabolisme : Myocarde, Oedème cardiaque.
- Animaux, Composés organiques du phosphore, Composés organométalliques, Diagnostic différentiel, Facteurs temps, Imagerie par résonance magnétique, Isotopes du sodium, Mâle, Perfusion, Produits de contraste, Rat Wistar, Rats, Spectroscopie par résonance magnétique, Techniques in vitro, Valeur prédictive des tests.
English descriptors
- KwdEn :
- Animals, Contrast Media, Diagnosis, Differential, Edema, Cardiac (diagnosis), Edema, Cardiac (metabolism), Edema, Cardiac (pathology), In Vitro Techniques, Magnetic Resonance Imaging, Magnetic Resonance Spectroscopy, Male, Myocardial Infarction (pathology), Myocardium (metabolism), Myocardium (pathology), Organometallic Compounds, Organophosphorus Compounds, Perfusion, Predictive Value of Tests, Rats, Rats, Wistar, Sodium Isotopes, Time Factors.
- MESH :
- chemical : Contrast Media, Organometallic Compounds, Organophosphorus Compounds, Sodium Isotopes.
- diagnosis : Edema, Cardiac.
- metabolism : Edema, Cardiac, Myocardium.
- pathology : Edema, Cardiac, Myocardial Infarction, Myocardium.
- Animals, Diagnosis, Differential, In Vitro Techniques, Magnetic Resonance Imaging, Magnetic Resonance Spectroscopy, Male, Perfusion, Predictive Value of Tests, Rats, Rats, Wistar, Time Factors.
Abstract
Myocardial edema can arise in several disease states. MRI contrast agent can accumulate in edematous tissue, which complicates differential diagnosis with contrast-enhanced (CE)-MRI and might lead to overestimation of infarct size. Sodium Chemical Shift Imaging ((23)Na-CSI) may provide an alternative for edema imaging. We have developed a non-infarct, isolated rat heart model with two levels of edema, which was studied with (23)Na-CSI and CE-MRI. In edematous, but viable tissue the extracellular sodium (Na (e) (+)) signal is hypothesized to increase, but not the intracellular sodium (Na (i) (+)) signal. Isolated hearts were perfused at 60 (n = 6) and 140 mmHg (n = 5). Dimethyl methylphosphonate (DMMP) and phenylphosphonate (PPA) were used to follow edema formation by (31)P-MR Spectroscopy. In separate groups, Thulium(III)1,4,7,10 tetraazacyclododecane-N,N',N″,N'''-tetra(methylenephosphonate) (TmDOTP(5-)) and Gadovist were used for (23)Na-CSI (n = 8) and CE-MRI (n = 6), respectively. PPA normalized signal intensity (SI) was higher at 140 versus 60 mmHg, with a ratio of 1.27 ± 0.12 (p < 0.05). The (DMMP-PPA)/dry weight ratio, as a marker of intracellular volume, remained unchanged. The mid-heart cross sectional area (CSA) of the left ventricle (LV) was significantly increased at 140 mmHg. In addition, at 140 mmHg, the LV Na (e) (+) SI increased with a 140 mmHg/60 mmHg ratio of 1.24 ± 0.18 (p < 0.05). Na (i) (+) SI remained essentially unchanged. With CE-MRI, a subendocardially enhanced CSA was identified, increasing from 0.20 ± 0.02 cm(2) at 60 mmHg to 0.31 ± 0.02 cm(2) at 140 mmHg (p < 0.05). Edema shows up in both CE-MRI and Na (e) (+) . High perfusion pressure causes more edema subendocardially than subepicardially. (23)Na-CSI is an attractive alternative for imaging of edema and is a promising tool to discriminate between edema, acute and chronic MI.
DOI: 10.1007/s10554-012-0093-6
PubMed: 22790331
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Van Echteld</name></author></analytic><series><title level="j">The international journal of cardiovascular imaging</title><idno type="eISSN">1875-8312</idno><imprint><date when="2013" type="published">2013</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Animals</term><term>Contrast Media</term><term>Diagnosis, Differential</term><term>Edema, Cardiac (diagnosis)</term><term>Edema, Cardiac (metabolism)</term><term>Edema, Cardiac (pathology)</term><term>In Vitro Techniques</term><term>Magnetic Resonance Imaging</term><term>Magnetic Resonance Spectroscopy</term><term>Male</term><term>Myocardial Infarction (pathology)</term><term>Myocardium (metabolism)</term><term>Myocardium (pathology)</term><term>Organometallic Compounds</term><term>Organophosphorus Compounds</term><term>Perfusion</term><term>Predictive Value of Tests</term><term>Rats</term><term>Rats, Wistar</term><term>Sodium Isotopes</term><term>Time Factors</term></keywords><keywords scheme="KwdFr" xml:lang="fr"><term>Animaux</term><term>Composés organiques du phosphore</term><term>Composés organométalliques</term><term>Diagnostic différentiel</term><term>Facteurs temps</term><term>Imagerie par résonance magnétique</term><term>Infarctus du myocarde (anatomopathologie)</term><term>Isotopes du sodium</term><term>Myocarde (anatomopathologie)</term><term>Myocarde (métabolisme)</term><term>Mâle</term><term>Oedème cardiaque (anatomopathologie)</term><term>Oedème cardiaque (diagnostic)</term><term>Oedème cardiaque (métabolisme)</term><term>Perfusion</term><term>Produits de contraste</term><term>Rat Wistar</term><term>Rats</term><term>Spectroscopie par résonance magnétique</term><term>Techniques in vitro</term><term>Valeur prédictive des tests</term></keywords><keywords scheme="MESH" type="chemical" xml:lang="en"><term>Contrast Media</term><term>Organometallic Compounds</term><term>Organophosphorus Compounds</term><term>Sodium Isotopes</term></keywords><keywords scheme="MESH" qualifier="anatomopathologie" xml:lang="fr"><term>Infarctus du myocarde</term><term>Myocarde</term><term>Oedème cardiaque</term></keywords><keywords scheme="MESH" qualifier="diagnosis" xml:lang="en"><term>Edema, Cardiac</term></keywords><keywords scheme="MESH" qualifier="diagnostic" xml:lang="fr"><term>Oedème cardiaque</term></keywords><keywords scheme="MESH" qualifier="metabolism" xml:lang="en"><term>Edema, Cardiac</term><term>Myocardium</term></keywords><keywords scheme="MESH" qualifier="métabolisme" xml:lang="fr"><term>Myocarde</term><term>Oedème cardiaque</term></keywords><keywords scheme="MESH" qualifier="pathology" xml:lang="en"><term>Edema, Cardiac</term><term>Myocardial Infarction</term><term>Myocardium</term></keywords><keywords scheme="MESH" xml:lang="en"><term>Animals</term><term>Diagnosis, Differential</term><term>In Vitro Techniques</term><term>Magnetic Resonance Imaging</term><term>Magnetic Resonance Spectroscopy</term><term>Male</term><term>Perfusion</term><term>Predictive Value of Tests</term><term>Rats</term><term>Rats, Wistar</term><term>Time Factors</term></keywords><keywords scheme="MESH" xml:lang="fr"><term>Animaux</term><term>Composés organiques du phosphore</term><term>Composés organométalliques</term><term>Diagnostic différentiel</term><term>Facteurs temps</term><term>Imagerie par résonance magnétique</term><term>Isotopes du sodium</term><term>Mâle</term><term>Perfusion</term><term>Produits de contraste</term><term>Rat Wistar</term><term>Rats</term><term>Spectroscopie par résonance magnétique</term><term>Techniques in vitro</term><term>Valeur prédictive des tests</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">Myocardial edema can arise in several disease states. MRI contrast agent can accumulate in edematous tissue, which complicates differential diagnosis with contrast-enhanced (CE)-MRI and might lead to overestimation of infarct size. Sodium Chemical Shift Imaging ((23)Na-CSI) may provide an alternative for edema imaging. We have developed a non-infarct, isolated rat heart model with two levels of edema, which was studied with (23)Na-CSI and CE-MRI. In edematous, but viable tissue the extracellular sodium (Na (e) (+)) signal is hypothesized to increase, but not the intracellular sodium (Na (i) (+)) signal. Isolated hearts were perfused at 60 (n = 6) and 140 mmHg (n = 5). Dimethyl methylphosphonate (DMMP) and phenylphosphonate (PPA) were used to follow edema formation by (31)P-MR Spectroscopy. In separate groups, Thulium(III)1,4,7,10 tetraazacyclododecane-N,N',N″,N'''-tetra(methylenephosphonate) (TmDOTP(5-)) and Gadovist were used for (23)Na-CSI (n = 8) and CE-MRI (n = 6), respectively. PPA normalized signal intensity (SI) was higher at 140 versus 60 mmHg, with a ratio of 1.27 ± 0.12 (p < 0.05). The (DMMP-PPA)/dry weight ratio, as a marker of intracellular volume, remained unchanged. The mid-heart cross sectional area (CSA) of the left ventricle (LV) was significantly increased at 140 mmHg. In addition, at 140 mmHg, the LV Na (e) (+) SI increased with a 140 mmHg/60 mmHg ratio of 1.24 ± 0.18 (p < 0.05). Na (i) (+) SI remained essentially unchanged. With CE-MRI, a subendocardially enhanced CSA was identified, increasing from 0.20 ± 0.02 cm(2) at 60 mmHg to 0.31 ± 0.02 cm(2) at 140 mmHg (p < 0.05). Edema shows up in both CE-MRI and Na (e) (+) . High perfusion pressure causes more edema subendocardially than subepicardially. (23)Na-CSI is an attractive alternative for imaging of edema and is a promising tool to discriminate between edema, acute and chronic MI.</div></front></TEI><pubmed><MedlineCitation Owner="NLM" Status="MEDLINE"><PMID Version="1">22790331</PMID><DateCreated><Year>2013</Year><Month>02</Month><Day>01</Day></DateCreated><DateCompleted><Year>2013</Year><Month>07</Month><Day>12</Day></DateCompleted><DateRevised><Year>2015</Year><Month>11</Month><Day>19</Day></DateRevised><Article PubModel="Print-Electronic"><Journal><ISSN IssnType="Electronic">1875-8312</ISSN><JournalIssue CitedMedium="Internet"><Volume>29</Volume><Issue>2</Issue><PubDate><Year>2013</Year><Month>Feb</Month></PubDate></JournalIssue><Title>The international journal of cardiovascular imaging</Title><ISOAbbreviation>Int J Cardiovasc Imaging</ISOAbbreviation></Journal><ArticleTitle>23Na chemical shift imaging and Gd enhancement of myocardial edema.</ArticleTitle><Pagination><MedlinePgn>343-54</MedlinePgn></Pagination><ELocationID EIdType="doi" ValidYN="Y">10.1007/s10554-012-0093-6</ELocationID><Abstract><AbstractText>Myocardial edema can arise in several disease states. MRI contrast agent can accumulate in edematous tissue, which complicates differential diagnosis with contrast-enhanced (CE)-MRI and might lead to overestimation of infarct size. Sodium Chemical Shift Imaging ((23)Na-CSI) may provide an alternative for edema imaging. We have developed a non-infarct, isolated rat heart model with two levels of edema, which was studied with (23)Na-CSI and CE-MRI. In edematous, but viable tissue the extracellular sodium (Na (e) (+)) signal is hypothesized to increase, but not the intracellular sodium (Na (i) (+)) signal. Isolated hearts were perfused at 60 (n = 6) and 140 mmHg (n = 5). Dimethyl methylphosphonate (DMMP) and phenylphosphonate (PPA) were used to follow edema formation by (31)P-MR Spectroscopy. In separate groups, Thulium(III)1,4,7,10 tetraazacyclododecane-N,N',N″,N'''-tetra(methylenephosphonate) (TmDOTP(5-)) and Gadovist were used for (23)Na-CSI (n = 8) and CE-MRI (n = 6), respectively. PPA normalized signal intensity (SI) was higher at 140 versus 60 mmHg, with a ratio of 1.27 ± 0.12 (p < 0.05). The (DMMP-PPA)/dry weight ratio, as a marker of intracellular volume, remained unchanged. The mid-heart cross sectional area (CSA) of the left ventricle (LV) was significantly increased at 140 mmHg. In addition, at 140 mmHg, the LV Na (e) (+) SI increased with a 140 mmHg/60 mmHg ratio of 1.24 ± 0.18 (p < 0.05). Na (i) (+) SI remained essentially unchanged. With CE-MRI, a subendocardially enhanced CSA was identified, increasing from 0.20 ± 0.02 cm(2) at 60 mmHg to 0.31 ± 0.02 cm(2) at 140 mmHg (p < 0.05). Edema shows up in both CE-MRI and Na (e) (+) . High perfusion pressure causes more edema subendocardially than subepicardially. (23)Na-CSI is an attractive alternative for imaging of edema and is a promising tool to discriminate between edema, acute and chronic MI.</AbstractText></Abstract><AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Aguor</LastName><ForeName>Eissa N E</ForeName><Initials>EN</Initials><AffiliationInfo><Affiliation>Laboratory of Experimental Cardiology, University Medical Center Utrecht (UMCU), Utrecht, The Netherlands. e.n.e.aguor@umcutrecht.nl</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>van de Kolk</LastName><ForeName>Cees W A</ForeName><Initials>CW</Initials></Author><Author ValidYN="Y"><LastName>Arslan</LastName><ForeName>Fatih</ForeName><Initials>F</Initials></Author><Author ValidYN="Y"><LastName>Nederhoff</LastName><ForeName>Marcel G J</ForeName><Initials>MG</Initials></Author><Author ValidYN="Y"><LastName>Doevendans</LastName><ForeName>Pieter A F M</ForeName><Initials>PA</Initials></Author><Author ValidYN="Y"><LastName>Pasterkamp</LastName><ForeName>Gerard</ForeName><Initials>G</Initials></Author><Author ValidYN="Y"><LastName>Strijkers</LastName><ForeName>Gustav J</ForeName><Initials>GJ</Initials></Author><Author ValidYN="Y"><LastName>van Echteld</LastName><ForeName>Cees J A</ForeName><Initials>CJ</Initials></Author></AuthorList><Language>eng</Language><PublicationTypeList><PublicationType UI="D003160">Comparative Study</PublicationType><PublicationType UI="D016428">Journal Article</PublicationType><PublicationType UI="D013485">Research Support, Non-U.S. Gov't</PublicationType></PublicationTypeList><ArticleDate DateType="Electronic"><Year>2012</Year><Month>07</Month><Day>12</Day></ArticleDate></Article><MedlineJournalInfo><Country>United States</Country><MedlineTA>Int J Cardiovasc Imaging</MedlineTA><NlmUniqueID>100969716</NlmUniqueID><ISSNLinking>1569-5794</ISSNLinking></MedlineJournalInfo><ChemicalList><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D003287">Contrast Media</NameOfSubstance></Chemical><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D009942">Organometallic Compounds</NameOfSubstance></Chemical><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D009943">Organophosphorus Compounds</NameOfSubstance></Chemical><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D012975">Sodium Isotopes</NameOfSubstance></Chemical><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="C069929">thulium(III) 1,4,7,10-tetraazacyclododecane-N,N',N'',N'''-tetramethylenephosphonate</NameOfSubstance></Chemical><Chemical><RegistryNumber>1BJ477IO2L</RegistryNumber><NameOfSubstance UI="C090600">gadobutrol</NameOfSubstance></Chemical></ChemicalList><CitationSubset>IM</CitationSubset><CommentsCorrectionsList><CommentsCorrections RefType="Cites"><RefSource>Magn Reson Med. 2001 Dec;46(6):1144-51</RefSource><PMID Version="1">11746581</PMID></CommentsCorrections><CommentsCorrections 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Wistar</DescriptorName></MeshHeading><MeshHeading><DescriptorName MajorTopicYN="Y" UI="D012975">Sodium Isotopes</DescriptorName></MeshHeading><MeshHeading><DescriptorName MajorTopicYN="N" UI="D013997">Time Factors</DescriptorName></MeshHeading></MeshHeadingList><OtherID Source="NLM">PMC3560947</OtherID></MedlineCitation><PubmedData><History><PubMedPubDate PubStatus="received"><Year>2012</Year><Month>4</Month><Day>5</Day></PubMedPubDate><PubMedPubDate PubStatus="accepted"><Year>2012</Year><Month>6</Month><Day>27</Day></PubMedPubDate><PubMedPubDate PubStatus="aheadofprint"><Year>2012</Year><Month>7</Month><Day>12</Day></PubMedPubDate><PubMedPubDate PubStatus="entrez"><Year>2012</Year><Month>7</Month><Day>14</Day><Hour>6</Hour><Minute>0</Minute></PubMedPubDate><PubMedPubDate PubStatus="pubmed"><Year>2012</Year><Month>7</Month><Day>14</Day><Hour>6</Hour><Minute>0</Minute></PubMedPubDate><PubMedPubDate 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