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Comparative analytical performance of multiple plasma Aß42 and Aß40 assays and their ability to predict positron emission tomography amyloid positivity.
Zicha, Stephen; Bateman, Randall J; Shaw, Leslie M; Zetterberg, Henrik; Bannon, Anthony W; Horton, Wesley A; Baratta, Mike; Kolb, Hartmuth C; Dobler, Iwona; Mordashova, Yulia; Saad, Ziad S; Raunig, David L; Spanakis, Emmanouil Manos; Li, Yan; Schindler, Suzanne E; Ferber, Kyle; Rubel, Carrie E; Martone, Robert L; Weber, Christopher J; Edelmayer, Rebecca M; Meyers, Emily A; Bollinger, James G; Rosenbaugh, Erin G; Potter, William Z.
Afiliação
  • Zicha S; Takeda, Pharmaceutical Company Ltd., Cambridge, Massachusetts, USA.
  • Bateman RJ; Department of Neurology, Washington University School of Medicine, St. Louis, Missouri, USA.
  • Shaw LM; Department of Pathology and Laboratory Medicine, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania, USA.
  • Zetterberg H; Institute of Neuroscience and Physiology, Department of Psychiatry and Neurochemistry, The Sahlgrenska Academy at University of Gothenburg, Mölndal, Sweden.
  • Bannon AW; Clinical Neurochemistry Laboratory, Sahlgrenska University Hospital, Mölndal, Sweden.
  • Horton WA; UK Dementia Research Institute Fluid Biomarkers Laboratory, UK DRI at UCL, London, UK.
  • Baratta M; Department of Neurodegenerative Disease, UCL Queen Square Institute of Neurology, London, UK.
  • Kolb HC; AbbVie, North Chicago, Illinois, USA.
  • Dobler I; The Foundation for the National Institutes of Health, North Bethesda, Maryland, USA.
  • Mordashova Y; Takeda, Pharmaceutical Company Ltd., Cambridge, Massachusetts, USA.
  • Saad ZS; Neuroscience Biomarkers, Janssen Research and Development LLC, La Jolla, California, USA.
  • Raunig DL; Takeda, Pharmaceutical Company Ltd., Cambridge, Massachusetts, USA.
  • Spanakis EM; AbbVie Deutschland GmbH & Co KG, Ludwigshafen, Germany.
  • Li Y; Neuroscience Biomarkers, Janssen Research and Development LLC, La Jolla, California, USA.
  • Schindler SE; Takeda, Pharmaceutical Company Ltd., Cambridge, Massachusetts, USA.
  • Ferber K; AbbVie Deutschland GmbH & Co KG, Ludwigshafen, Germany.
  • Rubel CE; Department of Neurology, Washington University School of Medicine, St. Louis, Missouri, USA.
  • Martone RL; Department of Neurology, Washington University School of Medicine, St. Louis, Missouri, USA.
  • Weber CJ; Biogen, Cambridge, Massachusetts, USA.
  • Edelmayer RM; Biogen, Cambridge, Massachusetts, USA.
  • Meyers EA; Biogen, Cambridge, Massachusetts, USA.
  • Bollinger JG; Alzheimer's Association, Chicago, Illinois, USA.
  • Rosenbaugh EG; Alzheimer's Association, Chicago, Illinois, USA.
  • Potter WZ; Alzheimer's Association, Chicago, Illinois, USA.
Alzheimers Dement ; 2022 Jul 12.
Article em En | MEDLINE | ID: mdl-35820077
ABSTRACT

INTRODUCTION:

This report details the approach taken to providing a dataset allowing for analyses on the performance of recently developed assays of amyloid beta (Aß) peptides in plasma and the extent to which they improve the prediction of amyloid positivity.

METHODS:

Alzheimer's Disease Neuroimaging Initiative plasma samples with corresponding amyloid positron emission tomography (PET) data were run on six plasma Aß assays. Statistical tests were performed to determine whether the plasmameasures significantly improved the area under the receiver operating characteristic curve for predicting amyloid PET status compared to age and apolipoprotein E (APOE) genotype.

RESULTS:

The age and APOE genotype model predicted amyloid status with an area under the curve (AUC) of 0.75. Three assays improved AUCs to 0.81, 0.81, and 0.84 (P < .05, uncorrected for multiple comparisons).

DISCUSSION:

Measurement of Aß in plasma contributes to addressing the amyloid component of the ATN (amyloid/tau/neurodegeneration) framework and could be a first step before or in place of a PET or cerebrospinal fluid screening study. HIGHLIGHTS The Foundation of the National Institutes of Health Biomarkers Consortium evaluated six plasma amyloid beta (Aß) assays using Alzheimer's Disease Neuroimaging Initiative samples. Three assays improved prediction of amyloid status over age and apolipoprotein E (APOE) genotype. Plasma Aß42/40 predicted amyloid positron emission tomography status better than Aß42 or Aß40 alone.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Estados Unidos