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Stress testing the Centiloid: Precision and variability of PET quantification of amyloid pathology.
Shekari, Mahnaz; Vállez García, David; Collij, Lyduine E; Altomare, Daniele; Heeman, Fiona; Pemberton, Hugh; Roé Vellvé, Núria; Bullich, Santiago; Buckley, Christopher; Stephens, Andrew; Farrar, Gill; Frisoni, Giovanni; Klunk, William E; Barkhof, Frederik; Gispert, Juan Domingo.
Afiliação
  • Shekari M; Barcelonaßeta Brain Research Center (BBRC), Pasqual Maragall Foundation, Barcelona, Spain.
  • Vállez García D; IMIM (Hospital del Mar Medical Research Institute), Barcelona, Spain.
  • Collij LE; Universitat Pompeu Fabra, Barcelona, Spain.
  • Altomare D; Department of Radiology and Nuclear Medicine, Amsterdam UMC, Vrije Universiteit Amsterdam, Amsterdam, Netherlands.
  • Heeman F; Department of Radiology and Nuclear Medicine, Amsterdam UMC, Vrije Universiteit Amsterdam, Amsterdam, Netherlands.
  • Pemberton H; Clinical Memory Research Unit, Clinical Sciences Malmö, Lund University, Malmö, Sweden.
  • Roé Vellvé N; Memory Center, Department of Rehabilitation and Geriatrics, University Hospitals and University of Geneva, Genève, Switzerland.
  • Bullich S; Department of Radiology and Nuclear Medicine, Amsterdam UMC, Vrije Universiteit Amsterdam, Amsterdam, Netherlands.
  • Buckley C; Wallenberg Centre for Molecular and Translational Medicine, University of Gothenburg, The University of Gothenburg, Gothenburg, Sweden.
  • Stephens A; Department of Psychiatry and Neurochemistry, University of Gothenburg, Sahlgrenska University Hospital, Gothenburg, Sweden.
  • Farrar G; GE Healthcare Life Sciences, Amersham, UK.
  • Frisoni G; Institute of Neurology and Centre for Medical Image Computing, University College London, London, UK.
  • Klunk WE; Life Molecular Imaging GmbH, Berlin, Germany.
  • Barkhof F; Life Molecular Imaging GmbH, Berlin, Germany.
  • Gispert JD; GE Healthcare Life Sciences, Amersham, UK.
Alzheimers Dement ; 2024 Jul 04.
Article em En | MEDLINE | ID: mdl-38961808
ABSTRACT

INTRODUCTION:

Assessing the potential sources of bias and variability of the Centiloid (CL) scale is fundamental for its appropriate clinical application.

METHODS:

We included 533 participants from AMYloid imaging to Prevent Alzheimer's Disease (AMYPAD DPMS) and Alzheimer's Disease Neuroimaging Initiative (ADNI) cohorts. Thirty-two CL pipelines were created using different combinations of reference region (RR), RR and target types, and quantification spaces. Generalized estimating equations stratified by amyloid positivity were used to assess the impact of the quantification pipeline, radiotracer, age, brain atrophy, and harmonization status on CL.

RESULTS:

RR selection and RR type impact CL the most, particularly in amyloid-negative individuals. The standard CL pipeline with the whole cerebellum as RR is robust against brain atrophy and differences in image resolution, with 95% confidence intervals below ± 3.95 CL for amyloid beta positivity cutoffs (CL < 24).

DISCUSSION:

The standard CL pipeline is recommended for most scenarios. Confidence intervals should be considered when operationalizing CL cutoffs in clinical and research settings. HIGHLIGHTS We developed a framework for evaluating Centiloid (CL) variability to different factors. Reference region selection and delineation had the highest impact on CL values. Whole cerebellum (WCB) and whole cerebellum plus brainstem (WCB+BSTM) as reference regions yielded consistent results across tracers. The standard CL pipeline is robust against atrophy and image resolution variation. Estimated within- and between-pipeline variability (95% confidence interval) in absolute CL units.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article