Accurate risk estimation of β-amyloid positivity to identify prodromal Alzheimer's disease: Cross-validation study of practical algorithms.


Journal

Alzheimer's & dementia : the journal of the Alzheimer's Association
ISSN: 1552-5279
Titre abrégé: Alzheimers Dement
Pays: United States
ID NLM: 101231978

Informations de publication

Date de publication:
02 2019
Historique:
received: 20 03 2018
revised: 14 06 2018
accepted: 21 08 2018
pubmed: 27 10 2018
medline: 11 4 2020
entrez: 27 10 2018
Statut: ppublish

Résumé

The aim was to create readily available algorithms that estimate the individual risk of β-amyloid (Aβ) positivity. The algorithms were tested in BioFINDER (n = 391, subjective cognitive decline or mild cognitive impairment) and validated in Alzheimer's Disease Neuroimaging Initiative (n = 661, subjective cognitive decline or mild cognitive impairment). The examined predictors of Aβ status were demographics; cognitive tests; white matter lesions; apolipoprotein E (APOE); and plasma Aβ Aβ status was accurately estimated in BioFINDER using age, 10-word delayed recall or Mini-Mental State Examination, and APOE (area under the receiver operating characteristics curve = 0.81 [0.77-0.85] to 0.83 [0.79-0.87]). When validated, the models performed almost identical in Alzheimer's Disease Neuroimaging Initiative (area under the receiver operating characteristics curve = 0.80-0.82) and within different age, subjective cognitive decline, and mild cognitive impairment populations. Plasma Aβ The algorithms are implemented on http://amyloidrisk.com where the individual probability of being Aβ positive can be calculated. This is useful in the workup of prodromal Alzheimer's disease and can reduce the number needed to screen in Alzheimer's disease trials.

Identifiants

pubmed: 30365928
pii: S1552-5260(18)33524-6
doi: 10.1016/j.jalz.2018.08.014
pmc: PMC6374284
pii:
doi:

Substances chimiques

Amyloid beta-Peptides 0
Apolipoproteins E 0
Biomarkers 0

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, U.S. Gov't, Non-P.H.S.

Langues

eng

Sous-ensembles de citation

IM

Pagination

194-204

Subventions

Organisme : NIA NIH HHS
ID : U01 AG024904
Pays : United States

Informations de copyright

Copyright © 2018 The Authors. Published by Elsevier Inc. All rights reserved.

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Auteurs

Sebastian Palmqvist (S)

Clinical Memory Research Unit, Department of Clinical Sciences, Lund University, Malmö, Sweden; Department of Neurology, Skåne University Hospital, Lund, Sweden. Electronic address: sebastian.palmqvist@med.lu.se.

Philip S Insel (PS)

Clinical Memory Research Unit, Department of Clinical Sciences, Lund University, Malmö, Sweden.

Henrik Zetterberg (H)

Department of Psychiatry and Neurochemistry, Institute of Neuroscience and Physiology, the Sahlgrenska Academy at the University of Gothenburg, Mölndal, Sweden; Clinical Neurochemistry Laboratory, Sahlgrenska University Hospital, Mölndal, Sweden; Department of Molecular Neuroscience, UCL Institute of Neurology, Queen Square, London, United Kingdom; UK Dementia Research Institute at UCL, London, United Kingdom.

Kaj Blennow (K)

Department of Psychiatry and Neurochemistry, Institute of Neuroscience and Physiology, the Sahlgrenska Academy at the University of Gothenburg, Mölndal, Sweden; Clinical Neurochemistry Laboratory, Sahlgrenska University Hospital, Mölndal, Sweden.

Britta Brix (B)

Euroimmun AG, Lübeck, Germany.

Erik Stomrud (E)

Clinical Memory Research Unit, Department of Clinical Sciences, Lund University, Malmö, Sweden; Memory Clinic, Skåne University Hospital, Malmö, Sweden.

Niklas Mattsson (N)

Clinical Memory Research Unit, Department of Clinical Sciences, Lund University, Malmö, Sweden; Department of Neurology, Skåne University Hospital, Lund, Sweden.

Oskar Hansson (O)

Clinical Memory Research Unit, Department of Clinical Sciences, Lund University, Malmö, Sweden; Memory Clinic, Skåne University Hospital, Malmö, Sweden. Electronic address: oskar.hansson@med.lu.se.

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