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dc.contributor.authorRos, D
dc.contributor.authorPavia, J
dc.contributor.authorCalviño Tavares, Francisco
dc.contributor.authorLomena, F
dc.contributor.authorCrespo, C
dc.contributor.authorGallego, J
dc.contributor.authorCot Sanz, Alberto
dc.contributor.authorFalcon, C
dc.contributor.authorBullich, S
dc.contributor.authorPareto, D
dc.contributor.authorAguiar, P
dc.contributor.authorSempau Roma, Josep
dc.contributor.otherUniversitat Politècnica de Catalunya. Departament de Física i Enginyeria Nuclear
dc.contributor.otherUniversitat Politècnica de Catalunya. Institut de Tècniques Energètiques
dc.date.accessioned2011-01-26T10:05:20Z
dc.date.available2011-01-26T10:05:20Z
dc.date.created2008-07
dc.date.issued2008-07
dc.identifier.citationCrespo, C. [et al.]. Quantification of dopaminergic neurotransmission SPECT studies with I-123-labelled radioligands. A comparison between different imaging systems and data acquisition protocols using Monte Carlo simulation. "European journal of nuclear medicine and molecular Imaging", Juliol 2008, vol. 35, núm. 7, p. 1334-1342.
dc.identifier.issn1619-7070
dc.identifier.urihttp://hdl.handle.net/2117/11209
dc.description.abstractPurpose 123I-labelled radioligands are commonly used for single-photon emission computed tomography (SPECT) imaging of the dopaminergic system to study the dopamine transporter binding. The aim of this work was to compare the quantitative capabilities of two different SPECT systems through Monte Carlo (MC) simulation. Methods The SimSET MC code was employed to generate simulated projections of a numerical phantom for two gamma cameras equipped with a parallel and a fan-beam collimator, respectively. A fully 3D iterative reconstruction algorithm was used to compensate for attenuation, the spatially variant point spread function (PSF) and scatter. A post-reconstruction partial volume effect (PVE) compensation was also developed. Results For both systems, the correction for all degradations and PVE compensation resulted in recovery factors of the theoretical specific uptake ratio (SUR) close to 100%. For a SUR value of 4, the recovered SUR for the parallel imaging system was 33% for a reconstruction without corrections (OSEM), 45%for a reconstruction with attenuation correction (OSEM-A), 56% for a 3D reconstruction with attenuation and PSF corrections (OSEM-AP), 68% for OSEM-AP with scatter correction (OSEM-APS) and 97% for OSEM-APS plus PVE compensation (OSEM-APSV). For the fan-beam imaging system, the recovered SUR was 41% without corrections, 55% for OSEM-A, 65% for OSEM-AP, 75% for OSEM-APS and 102% for OSEM-APSV. Conclusion Our findings indicate that the correction for degradations increases the quantification accuracy, with PVE compensation playing a major role in the SUR quantification. The proposed methodology allows us to reach similar SUR values for different SPECT systems, thereby allowing a reliable standardisation in multicentric studies.
dc.format.extent9 p.
dc.language.isoeng
dc.rightsAttribution-NonCommercial-NoDerivs 3.0 Spain
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/es/
dc.subjectÀrees temàtiques de la UPC::Energies::Tecnologia energètica
dc.subject.lcshMonte Carlo method
dc.subject.lcshTomography
dc.titleQuantification of dopaminergic neurotransmission SPECT studies with I-123-labelled radioligands. A comparison between different imaging systems and data acquisition protocols using Monte Carlo simulation
dc.typeArticle
dc.subject.lemacMonte Carlo, Mètode de
dc.subject.lemacTomografia
dc.contributor.groupUniversitat Politècnica de Catalunya. GREENER - Grup de recerca d'estudis energètics i de les radiacions
dc.identifier.doi10.1007/s00259-007-0711-z
dc.description.peerreviewedPeer Reviewed
dc.rights.accessRestricted access - publisher's policy
local.identifier.drac1247861
dc.description.versionPostprint (published version)
local.citation.authorCrespo, C.; Gallego, J.; Cot, A.; Falcon, C.; Bullich, S.; Pareto, D.; Aguiar, P.; Sempau, J.; Lomena, F.; Calviño, F.; Pavia, J.; Ros, D.
local.citation.publicationNameEuropean journal of nuclear medicine and molecular Imaging
local.citation.volume35
local.citation.number7
local.citation.startingPage1334
local.citation.endingPage1342


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