Optimized dual-time-window protocols for quantitative [

Alzheimer’s disease Amyloid Florbetaben PET Flutemetamol PET Quantification Simplified methods

Journal

EJNMMI research
ISSN: 2191-219X
Titre abrégé: EJNMMI Res
Pays: Germany
ID NLM: 101560946

Informations de publication

Date de publication:
27 Mar 2019
Historique:
received: 30 11 2018
accepted: 11 03 2019
entrez: 29 3 2019
pubmed: 29 3 2019
medline: 29 3 2019
Statut: epublish

Résumé

A long dynamic scanning protocol may be required to accurately measure longitudinal changes in amyloid load. However, such a protocol results in a lower patient comfort and scanning efficiency compared to static scans. A compromise can be achieved by implementing dual-time-window protocols. This study aimed to optimize these protocols for quantitative [ Rate constants for subjects across the Alzheimer's disease spectrum (i.e., non-displaceable binding potential (BP [ The length of the interval inversely correlates with the accuracy of the BP

Sections du résumé

BACKGROUND BACKGROUND
A long dynamic scanning protocol may be required to accurately measure longitudinal changes in amyloid load. However, such a protocol results in a lower patient comfort and scanning efficiency compared to static scans. A compromise can be achieved by implementing dual-time-window protocols. This study aimed to optimize these protocols for quantitative [
METHODS METHODS
Rate constants for subjects across the Alzheimer's disease spectrum (i.e., non-displaceable binding potential (BP
RESULTS RESULTS
[
CONCLUSIONS CONCLUSIONS
The length of the interval inversely correlates with the accuracy of the BP

Identifiants

pubmed: 30919133
doi: 10.1186/s13550-019-0499-4
pii: 10.1186/s13550-019-0499-4
pmc: PMC6437225
doi:

Types de publication

Journal Article

Langues

eng

Pagination

32

Subventions

Organisme : Innovative Medicines Initiative
ID : 115952
Organisme : Ramón y Cajal
ID : RYC-2013-13054

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Auteurs

Fiona Heeman (F)

Amsterdam UMC, Vrije Universiteit Amsterdam, Radiology and Nuclear Medicine, Amsterdam Neuroscience, De Boelelaan, 1117, Amsterdam, Netherlands. f.heeman@vumc.nl.

Maqsood Yaqub (M)

Amsterdam UMC, Vrije Universiteit Amsterdam, Radiology and Nuclear Medicine, Amsterdam Neuroscience, De Boelelaan, 1117, Amsterdam, Netherlands.

Isadora Lopes Alves (I)

Amsterdam UMC, Vrije Universiteit Amsterdam, Radiology and Nuclear Medicine, Amsterdam Neuroscience, De Boelelaan, 1117, Amsterdam, Netherlands.

Kerstin Heurling (K)

Wallenberg Centre for Molecular and Translational Medicine and the Department of Psychiatry and Neurochemistry, University of Gothenburg, 405 30, Gothenburg, Sweden.

Johannes Berkhof (J)

Amsterdam UMC, Vrije Universiteit Amsterdam, Epidemiology and Biostatistics, De Boelelaan, 1117, Amsterdam, Netherlands.

Juan Domingo Gispert (JD)

Barcelonaβeta Brain Research Center, Pasqual Maragall Foundation, Carrer de Wellington, 30, 08005, Barcelona, Spain.
Centro de Investigación Biomédica en Red de Bioingeniería, Biomateriales y Nanomedicina (CIBER-BBN), Av. Monforte de Lemos, 3-5. Pabellón 11. Planta 0, 28029, Madrid, Spain.
Universitat Pompeu Fabra, Plaça de la Mercè, 10, 08002, Barcelona, Spain.

Santiago Bullich (S)

Life Molecular Imaging GmbH, Tegeler Str. 7, 13353, Berlin, Germany.

Christopher Foley (C)

GE Healthcare, Little Chalfont, Amersham, HP7 9NA, UK.

Adriaan A Lammertsma (AA)

Amsterdam UMC, Vrije Universiteit Amsterdam, Radiology and Nuclear Medicine, Amsterdam Neuroscience, De Boelelaan, 1117, Amsterdam, Netherlands.

Classifications MeSH