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Assessment of myocardial oxidative metabolism in aortic valve disease using positron emission tomography with C-11 acetate

dc.contributor.authorHicks, Rodney J.en_US
dc.contributor.authorSavas, Vickyen_US
dc.contributor.authorCurrie, Philip J.en_US
dc.contributor.authorKalff, Victoren_US
dc.contributor.authorStarling, Mark R.en_US
dc.contributor.authorBergin, Peteren_US
dc.contributor.authorKirsch, Marvin M.en_US
dc.contributor.authorSchwaiger, Markusen_US
dc.date.accessioned2006-04-10T15:19:28Z
dc.date.available2006-04-10T15:19:28Z
dc.date.issued1992-03en_US
dc.identifier.citationHicks, Rodney J., Savas, Vicky, Currie, Philip J., Kalff, Victor, Starling, Mark, Bergin, Peter, Kirsch, Marvin, Schwaiger, Markus (1992/03)."Assessment of myocardial oxidative metabolism in aortic valve disease using positron emission tomography with C-11 acetate." American Heart Journal 123(3): 653-664. <http://hdl.handle.net/2027.42/30196>en_US
dc.identifier.urihttp://www.sciencedirect.com/science/article/B6W9H-4BT89SH-4S/2/00d2087cefcbda09fe6faab8d0e06d37en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/30196
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=1539517&dopt=citationen_US
dc.description.abstractC-11 acetate has recently been introduced as a tracer of myocardial oxidative metabolism with the use of positron emission tomography. To evaluate this approach in the pressure- or volume-loaded heart, C-11 acetate clearance rate constants were determined in 22 patients with chronic aortic valve disease and in nine normal subjects. Global myocardial C-11 clearance was significantly higher in patients with predominant aortic stenosis (n = 11) or aortic regurgitation (n = 11) than in normal subjects (0.069 +/- 0.017 min-1 and 0.072 +/- 0.010 min-1 compared with 0.050 +/- 0.004 min-1, p r = 0.73, P = 0.0001) for all studies. However, analysis of patient subgroups demonstrated that this correlation held only for aortic stenosis (r = 0.79, p r = 0.89, p &lt; 0.005) but not in patients with aortic regurgitation. Normalization of C-11 acetate clearance rate constants for gradient-corrected rate-pressure product were significantly lower in patients with loaded ventricles, particularly in the presence of a low ejection fraction, compared to normal subjects. Possible mechanisms include myocardial adaptation through hypertrophy or depressed contractility, which would both tend to reduce oxygen consumption under any given load. Serial comparison of C-11 acetate kinetics and noninvasive indexes of oxygen demand may provide assessment of disease progression in pathologic ventricular loading.en_US
dc.format.extent2870648 bytes
dc.format.extent3118 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherElsevieren_US
dc.titleAssessment of myocardial oxidative metabolism in aortic valve disease using positron emission tomography with C-11 acetateen_US
dc.typeArticleen_US
dc.rights.robotsIndexNoFollowen_US
dc.subject.hlbsecondlevelInternal Medicine and Specialtiesen_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, Ann Arbor, Mich., USA.en_US
dc.contributor.affiliationumDivision of Nuclear Medicine, Department of Internal Medicine, University of Michigan Medical Center, Ann Arbor, Mich., USA.en_US
dc.contributor.affiliationumDivision of Nuclear Medicine, Department of Internal Medicine, University of Michigan Medical Center, Ann Arbor, Mich., USA.en_US
dc.contributor.affiliationumDivision of Nuclear Medicine, Department of Internal Medicine, University of Michigan Medical Center, Ann Arbor, Mich., USA.en_US
dc.contributor.affiliationumDivision of Nuclear Medicine, Department of Internal Medicine, University of Michigan Medical Center, Ann Arbor, Mich., USA.en_US
dc.contributor.affiliationumDivision of Nuclear Medicine, Department of Internal Medicine, University of Michigan Medical Center, Ann Arbor, Mich., USA.en_US
dc.contributor.affiliationumDivision of Nuclear Medicine, Department of Internal Medicine, University of Michigan Medical Center, Ann Arbor, Mich., USA.en_US
dc.contributor.affiliationumDivision of Nuclear Medicine, Department of Internal Medicine, University of Michigan Medical Center, Ann Arbor, Mich., USA.en_US
dc.identifier.pmid1539517en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/30196/1/0000584.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1016/0002-8703(92)90503-Nen_US
dc.identifier.sourceAmerican Heart Journalen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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