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Imaging of metabolism and autonomic innervation of the heart by positron emission tomography

dc.contributor.authorSchwaiger, Markusen_US
dc.contributor.authorMélon, Pierreen_US
dc.date.accessioned2006-09-11T18:15:32Z
dc.date.available2006-09-11T18:15:32Z
dc.date.issued1992-06en_US
dc.identifier.citationMélon, Pierre; Schwaiger, Markus; (1992). "Imaging of metabolism and autonomic innervation of the heart by positron emission tomography." European Journal of Nuclear Medicine 19(6): 453-464. <http://hdl.handle.net/2027.42/46833>en_US
dc.identifier.issn0340-6997en_US
dc.identifier.issn1619-7089en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/46833
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=1618239&dopt=citationen_US
dc.description.abstractPositron emission tomography (PET) allows, in combination with multiple radiopharmaceuticals, unique physiological and biochemical tissue characterization. Tracers of blood flow, metabolism and neuronal function have been employed with this technique for research application. More recently, PET has emerged in cardiology as a useful tool for the detection of coronary artery disease and the evaluation of tissue viability. Metabolic tracers such as fluorine-18 deoxyglucose (FDG) permit the specific delineation of ischaemically compromised myocardium. Clinical studies have indicated that the metabolic imaging is helpful in selecting patients for coronary artery bypass surgery or coronary angioplasty. More recent research work has concentrated on the use of carbon-11 acetate as a marker of myocardial oxygen consumption. Together with measurements of left ventricular performance, estimates of cardiac efficiency can be derived from dynamic 11 C-acetate studies. The non-invasive evaluation of the autonomic nervous system of the heart was limited in the past. With the introduction of radiopharmaceuticals which specifically bind to neuronal structures, the regional integrity of the autonomic nervous system of the heart can be evaluated with PET. Numerous tracers for pre- and postsynaptic binding sites have been synthesized. 11 C-hydroxyephedrine represents a new catecholamine analogue which is stored in cardiac presynaptic sympathetic nerve terminals. Initial clinical studies with it suggest a promising role for PET in the study of the sympathetic nervous system in various cardiac diseases such as cardiomyopathy, ischaemic heart disease and diabetes mellitus. The specificity of the radiopharmaceuticals and the quantitative measurements of tissue tracer distribution provided by PET make this technology a very attractive research tool in the cardiovascular sciences with great promise in the area of cardiac metabolism and neurocardiology.en_US
dc.format.extent3127084 bytes
dc.format.extent3115 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherSpringer-Verlagen_US
dc.subject.otherMedicine & Public Healthen_US
dc.subject.otherNuclear Medicineen_US
dc.subject.otherCardiacen_US
dc.subject.otherCardiac Autonomic Innervationen_US
dc.subject.otherImaging / Radiologyen_US
dc.subject.otherPositron Emission Tomographyen_US
dc.subject.otherMetabolismen_US
dc.titleImaging of metabolism and autonomic innervation of the heart by positron emission tomographyen_US
dc.typeArticleen_US
dc.subject.hlbsecondlevelRadiologyen_US
dc.subject.hlbsecondlevelPhysicsen_US
dc.subject.hlbsecondlevelBiological Chemistryen_US
dc.subject.hlbtoplevelScienceen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumDivision of Nuclear Medicine, Department of Internal Medicine, University of Michigan Medical Center, 1500 E. Medical Center Drive, UH BIG412, 48109-0028, Ann Arbor, MI, USAen_US
dc.contributor.affiliationumDivision of Nuclear Medicine, Department of Internal Medicine, University of Michigan Medical Center, 1500 E. Medical Center Drive, UH BIG412, 48109-0028, Ann Arbor, MI, USAen_US
dc.contributor.affiliationumcampusAnn Arboren_US
dc.identifier.pmid1618239en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/46833/1/259_2004_Article_BF00177375.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1007/BF00177375en_US
dc.identifier.sourceEuropean Journal of Nuclear Medicineen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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