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Quantitative characterization of hemodynamic properties and vasculature dysfunction of high-grade gliomas

dc.contributor.authorNagesh, Vijayaen_US
dc.contributor.authorChenevert, Thomas L.en_US
dc.contributor.authorTsien, Christina I.en_US
dc.contributor.authorRoss, Brian D.en_US
dc.contributor.authorLawrence, Theodore S.en_US
dc.contributor.authorJunck, Larryen_US
dc.contributor.authorCao, Yueen_US
dc.date.accessioned2007-09-20T19:07:10Z
dc.date.available2008-11-05T15:05:43Zen_US
dc.date.issued2007-10en_US
dc.identifier.citationNagesh, Vijaya; Chenevert, Thomas L.; Tsien, Christina I.; Ross, Brian D.; Lawrence, Theodore S.; Junck, Larry; Cao, Yue (2007)."Quantitative characterization of hemodynamic properties and vasculature dysfunction of high-grade gliomas." NMR in Biomedicine 20(6): 566-577. <http://hdl.handle.net/2027.42/56144>en_US
dc.identifier.issn0952-3480en_US
dc.identifier.issn1099-1492en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/56144
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=17221937&dopt=citation
dc.description.abstractAberrations in tumor and peritumoral vasculature may not be distinguishable by cerebral blood flow (CBF) or cerebral blood volume (CBV) alone. The relationships between CBF and CBV were examined to estimate vasculature-specific hemodynamic characteristics. Twenty glioma patients were studied with dynamic susceptibility T 2 *-weighted MRI [(dynamic contrast-enhanced magnetic resonance imaging (DSC-MRI)] before and during week 1 and 3 of radiotherapy (RT). CBF and CBV were calculated from DSC-MRI, and relationships between the two were evaluated: the physiological measure of mean transit time (MTT) = CBV/CBF; empirical fitting using the power law CBV = constant × (CBF) Β . Three different tissue types were assessed: the Gd-enhancing tumor volume (GEV); non-enhanced abnormal tissue located beyond GEV but within the abnormal hyperintense region on FLAIR images (NEV); normal tissue in the hemisphere contralateral to the tumor (CNT). The effects of tissue types, CBV magnitudes (low, medium and high), before and during RT, on MTT and Β were analyzed by analysis of variance (ANOVA). The MTT and Β for the three tissue types were significantly different ( p  < 0.009). MTT increased from CNT (1.60 s) to NEV (1.93 s) to GEV (2.28 s) ( p  < 0.0005). Β was significantly greater in GEV (1.079) and NEV (1.070) than in CNT (1.025). Β increased with increasing CBV magnitude while MTT was independent of CBV magnitude. There was a significant decrease in MTT of NEV and GEV during week 3 of RT compared with pre-RT values for all CBV magnitudes. There was a significant increase in Β during RT in the tumor and peritumor. Progressive abnormalities in vasculature and hemodynamic characteristics of the vascular bed were delineated, with significant disorder in the tumor but mild abnormality in peritumoral tissue. Copyright © 2007 John Wiley & Sons, Ltd.en_US
dc.format.extent338679 bytes
dc.format.extent3118 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.publisherJohn Wiley & Sons, Ltd.en_US
dc.subject.otherChemistryen_US
dc.subject.otherAnalytical Chemistry and Spectroscopyen_US
dc.titleQuantitative characterization of hemodynamic properties and vasculature dysfunction of high-grade gliomasen_US
dc.typeArticleen_US
dc.rights.robotsIndexNoFollowen_US
dc.subject.hlbsecondlevelElectrical Engineeringen_US
dc.subject.hlbsecondlevelPhysicsen_US
dc.subject.hlbtoplevelEngineeringen_US
dc.subject.hlbtoplevelScienceen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumDepartment of Radiation Oncology, University of Michigan, Ann Arbor, MI, USAen_US
dc.contributor.affiliationumDepartment of Radiology, University of Michigan, Ann Arbor, MI, USAen_US
dc.contributor.affiliationumDepartment of Radiation Oncology, University of Michigan, Ann Arbor, MI, USAen_US
dc.contributor.affiliationumDepartment of Radiology, University of Michigan, Ann Arbor, MI, USAen_US
dc.contributor.affiliationumDepartment of Radiation Oncology, University of Michigan, Ann Arbor, MI, USAen_US
dc.contributor.affiliationumDepartment of Neurology, University of Michigan, Ann Arbor, MI, USAen_US
dc.contributor.affiliationumDepartment of Radiation Oncology, University of Michigan, Ann Arbor, MI, USA ; Department of Radiology, University of Michigan, Ann Arbor, MI, USA ; Department of Radiation Oncology, University of Michigan, 1500 E. Medical Center Drive, UH. B2C438, Box 0010, Ann Arbor, MI 48109-0010, USA.en_US
dc.identifier.pmid17221937
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/56144/1/1118_ftp.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1002/nbm.1118en_US
dc.identifier.sourceNMR in Biomedicineen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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