European journal of nuclear medicine and molecular imaging · 2002
Quantification of [(123)I]PE2I binding to dopamine transporters with SPET.
Клиническое исследованиеСтатьяПоддержка исследования: вне правительства СШАНазвание и аннотация: Перевод в очереди
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Pinborg Lars H, Videbaek Charlotte, Svarer Claus, Yndgaard Stig, Paulson Olaf B, Knudsen Gitte M
Аннотация
The iodinated cocaine derivative [(123)I]PE2I is a new selective ligand for in vivo studies of the dopamine transporter (DAT) with single-photon emission tomography (SPET). The aim of the present study was to describe a method for accurate quantification of binding data following a bolus injection of [(123)I]PE2I. Six healthy subjects (age 51+/-24 years) underwent xenon-133 SPET for quantification of regional CBF and [(123)I]PE2I SPET for quantification of DAT binding. rCBFs were within normal limits in all subjects. Fitting data to a two-tissue compartment model resulted in striatal K(1) values of 0.39+/-0.08 ml ml(-1) min(-1), equal to a first-pass extraction fraction of 0.72+/-0.13. Distribution volumes (DVs) were calculated using compartment analysis, area under the curve analysis and Logan analysis. Logan analysis is preferred since stable DV values were already obtained 120 min after [(123)I]PE2I injection. Mean striatal DV was 37.9+/-9.6 ml ml(-1) and mean occipital cortex DV was 5.5+/-0.7 ml ml(-1). In the absence of local pathology in a reference tissue, Logan analysis without blood sampling is an attractive method for accurate quantification of striatal [(123)I]PE2I binding. The distribution volume ratio (DVR) (6.6+/-1.4) was in good agreement with the DVR calculated with blood (6.7+/-1.4).
Предметные рубрики MeSH
Area Under CurveCerebral CortexCerebrovascular CirculationCorpus StriatumDopamine Plasma Membrane Transport ProteinsHumansMembrane GlycoproteinsMembrane Transport ProteinsMiddle AgedModels, BiologicalModels, ChemicalNerve Tissue ProteinsNortropanesPhantoms, ImagingRadiopharmaceuticalsSensitivity and SpecificityTissue DistributionTomography, Emission-Computed, Single-PhotonXenon Radioisotopes