Please use this identifier to cite or link to this item: http://doi.org/10.25358/openscience-5879
Full metadata record
DC FieldValueLanguage
dc.contributor.authorGonzalez-Escamilla, Gabriel-
dc.contributor.authorMiederer, Isabelle-
dc.contributor.authorGrothe, Michel J.-
dc.contributor.authorSchreckenberger, Mathias-
dc.contributor.authorMuthuraman, Muthuraman-
dc.contributor.authorGroppa, Sergiu-
dc.date.accessioned2021-05-10T08:23:01Z-
dc.date.available2021-05-10T08:23:01Z-
dc.date.issued2021-
dc.identifier.urihttps://openscience.ub.uni-mainz.de/handle/20.500.12030/5888-
dc.description.abstractAlzheimer’s disease (AD) is a neurodegenerative disorder, considered a disconnection syndrome with regional molecular pattern abnormalities quantifiable by the aid of PET imaging. Solutions for accurate quantification of network dysfunction are scarce. We evaluate the extent to which PET molecular markers reflect quantifiable network metrics derived through the graph theory framework and how partial volume effects (PVE)-correction (PVEc) affects these PET-derived metrics 75 AD patients and 126 cognitively normal older subjects (CN). Therefore our goal is twofold: 1) to evaluate the differential patterns of [18F]FDG- and [18F]AV45-PET data to depict AD pathology; and ii) to analyse the effects of PVEc on global uptake measures of [18F]FDG- and [18F]AV45-PET data and their derived covariance network reconstructions for differentiating between patients and normal older subjects. Network organization patterns were assessed using graph theory in terms of “degree”, “modularity”, and “efficiency”. PVEc evidenced effects on global uptake measures that are specific to either [18F]FDG- or [18F]AV45-PET, leading to increased statistical differences between the groups. PVEc was further shown to influence the topological characterization of PET-derived covariance brain networks, leading to an optimised characterization of network efficiency and modularisation. Partial-volume effects correction improves the interpretability of PET data in AD and leads to optimised characterization of network properties for organisation or disconnection.en_GB
dc.language.isoengde
dc.rightsCC BY*
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/*
dc.subject.ddc610 Medizinde_DE
dc.subject.ddc610 Medical sciencesen_GB
dc.titleMetabolic and amyloid PET network reorganization in Alzheimer’s disease : differential patterns and partial volume effectsen_GB
dc.typeZeitschriftenaufsatzde
dc.identifier.doihttp://doi.org/10.25358/openscience-5879-
jgu.type.dinitypearticleen_GB
jgu.type.versionPublished versionde
jgu.type.resourceTextde
jgu.organisation.departmentFB 04 Medizinde
jgu.organisation.number2700-
jgu.organisation.nameJohannes Gutenberg-Universität Mainz-
jgu.rights.accessrightsopenAccess-
jgu.journal.titleBrain imaging and behaviorde
jgu.journal.volume15de
jgu.pages.start190de
jgu.pages.end204de
jgu.publisher.year2021-
jgu.publisher.nameSpringerde
jgu.publisher.placeNew York, NY u.a.de
jgu.publisher.urihttps://doi.org/10.1007/s11682-019-00247-9de
jgu.publisher.issn1931-7565de
jgu.organisation.placeMainz-
jgu.subject.ddccode610de
jgu.publisher.doi10.1007/s11682-019-00247-9
jgu.organisation.rorhttps://ror.org/023b0x485
Appears in collections:JGU-Publikationen

Files in This Item:
  File Description SizeFormat
Thumbnail
gonzalez-escamilla_gabriel-metabolic_and_-20210503155811443.pdf7.02 MBAdobe PDFView/Open