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Striatal monoamine terminals in Lewy body dementia and Alzheimer's disease

dc.contributor.authorGilman, Siden_US
dc.contributor.authorKoeppe, Robert A.en_US
dc.contributor.authorLittle, Roderick J. A.en_US
dc.contributor.authorAn, Hyongginen_US
dc.contributor.authorJunck, Larryen_US
dc.contributor.authorGiordani, Brunoen_US
dc.contributor.authorPersad, Carolen_US
dc.contributor.authorHeumann, Maryen_US
dc.contributor.authorWernette, Krisen_US
dc.date.accessioned2006-04-19T13:56:47Z
dc.date.available2006-04-19T13:56:47Z
dc.date.issued2004-06en_US
dc.identifier.citationGilman, Sid; Koeppe, Robert A.; Little, Roderick; An, Hyonggin; Junck, Larry; Giordani, Bruno; Persad, Carol; Heumann, Mary; Wernette, Kris (2004)."Striatal monoamine terminals in Lewy body dementia and Alzheimer's disease." Annals of Neurology 55(6): 774-780. <http://hdl.handle.net/2027.42/34891>en_US
dc.identifier.issn0364-5134en_US
dc.identifier.issn1531-8249en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/34891
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=15174011&dopt=citationen_US
dc.description.abstractWe used positron emission tomography (PET) with (+)-[ 11 C]dihydrotetrabenazine ([+]-[ 11 C]DTBZ) to examine striatal monoaminergic presynaptic terminal density in 20 patients with dementia with Lewy bodies (DLB), 25 with Alzheimer's disease (AD), and 19 normal elderly controls. Six DLB patients developed parkinsonism at least 1 year before dementia (DLB/PD) and 14 developed dementia before parkinsonism or at about the same time (DLB/AD). Striatal mean binding potential was decreased by 62 to 77% in the DLB/PD group and 45 to 67% in the DLB/AD compared to AD and control. Binding was lower in the DLB/PD group than the DLB/AD, but the differences reached only marginal significance in the caudate nucleus. No differences were found between AD and control groups though a few AD patients had binding values below the range of the controls. Subsequent neuropathological examination in one AD patient revealed both AD and DLB changes despite the absence of clinical parkinsonism. Both DLB groups had an anterior to posterior binding deficit gradient relative to controls, largest in posterior putamen, smaller in anterior putamen, smallest in caudate nucleus. The DLB/AD group showed significant binding asymmetry only in posterior putamen. We conclude that PET with (+)-[ 11 C]DTBZ differentiates DLB from AD, and decreased binding in AD may indicate subclinical DLB pathology in addition to AD pathology. Ann Neurol 2004en_US
dc.format.extent91362 bytes
dc.format.extent3118 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherWiley Subscription Services, Inc., A Wiley Companyen_US
dc.subject.otherLife and Medical Sciencesen_US
dc.subject.otherNeuroscience, Neurology, and Psychiatryen_US
dc.titleStriatal monoamine terminals in Lewy body dementia and Alzheimer's diseaseen_US
dc.typeArticleen_US
dc.rights.robotsIndexNoFollowen_US
dc.subject.hlbsecondlevelPsychiatryen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumDepartment of Neurology, Division of Nuclear Medicine, University of Michigan, Ann Arbor, MI ; Department of Neurology, University of Michigan Health System, 1500 E. Medical Center Drive, Ann Arbor, MI 48109-0316en_US
dc.contributor.affiliationumDepartment of Radiology, University of Michigan, Ann Arbor, MIen_US
dc.contributor.affiliationumDepartment of Biostatistics, University of Michigan, Ann Arbor, MIen_US
dc.contributor.affiliationumDepartment of Biostatistics, University of Michigan, Ann Arbor, MIen_US
dc.contributor.affiliationumDepartment of Neurology, Division of Nuclear Medicine, University of Michigan, Ann Arbor, MIen_US
dc.contributor.affiliationumDepartment of Psychiatry, University of Michigan, Ann Arbor, MIen_US
dc.contributor.affiliationumDepartment of Psychiatry, University of Michigan, Ann Arbor, MIen_US
dc.contributor.affiliationumDepartment of Neurology, Division of Nuclear Medicine, University of Michigan, Ann Arbor, MIen_US
dc.contributor.affiliationumDepartment of Neurology, Division of Nuclear Medicine, University of Michigan, Ann Arbor, MIen_US
dc.identifier.pmid15174011en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/34891/1/20088_ftp.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1002/ana.20088en_US
dc.identifier.sourceAnnals of Neurologyen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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