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The Canadian Dementia Imaging Protocol: Harmonization validity for morphometry measurements

The harmonized Canadian Dementia Imaging Protocol (CDIP) has been developed to suit the needs of a number of co-occurring Canadian studies collecting data on brain changes across adulthood and neurodegeneration. In this study, we verify the impact of CDIP parameters compliance on total brain volume...

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Detalles Bibliográficos
Autores principales: Potvin, Olivier, Chouinard, Isabelle, Dieumegarde, Louis, Bartha, Robert, Bellec, Pierre, Collins, D. Louis, Descoteaux, Maxime, Hoge, Rick, Ramirez, Joel, Scott, Christopher J.M., Smith, Eric E., Strother, Stephen C., Black, Sandra E., Duchesne, Simon
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6661407/
https://www.ncbi.nlm.nih.gov/pubmed/31351228
http://dx.doi.org/10.1016/j.nicl.2019.101943
Descripción
Sumario:The harmonized Canadian Dementia Imaging Protocol (CDIP) has been developed to suit the needs of a number of co-occurring Canadian studies collecting data on brain changes across adulthood and neurodegeneration. In this study, we verify the impact of CDIP parameters compliance on total brain volume variance using 86 scans of the same individual acquired on various scanners. Data included planned data collection acquired within the Consortium pour l'identification précoce de la maladie Alzheimer - Québec (CIMA-Q) and Canadian Consortium on Neurodegeneration in Aging (CCNA) studies, as well as opportunistic data collection from various protocols. For images acquired from Philips scanners, lower variance in brain volumes were observed when the stated CDIP resolution was set. For images acquired from GE scanners, lower variance in brain volumes were noticed when TE/TR values were within 5% of the CDIP protocol, compared to values farther from that criteria. Together, these results suggest that a harmonized protocol like the CDIP may help to reduce neuromorphometric measurement variability in multi-centric studies.