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Added value of amyloid PET in individualized risk predictions for MCI patients

INTRODUCTION: To construct a prognostic model based on amyloid positron emission tomography (PET) to predict clinical progression in individual patients with mild cognitive impairment (MCI). METHODS: We included 411 MCI patients from the Alzheimer's Disease Neuroimaging Initiative. Prognostic m...

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Autores principales: van Maurik, Ingrid S., van der Kall, Laura M., de Wilde, Arno, Bouwman, Femke H., Scheltens, Philip, van Berckel, Bart N.M., Berkhof, Johannes, van der Flier, Wiesje M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6667768/
https://www.ncbi.nlm.nih.gov/pubmed/31388557
http://dx.doi.org/10.1016/j.dadm.2019.04.011
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author van Maurik, Ingrid S.
van der Kall, Laura M.
de Wilde, Arno
Bouwman, Femke H.
Scheltens, Philip
van Berckel, Bart N.M.
Berkhof, Johannes
van der Flier, Wiesje M.
author_facet van Maurik, Ingrid S.
van der Kall, Laura M.
de Wilde, Arno
Bouwman, Femke H.
Scheltens, Philip
van Berckel, Bart N.M.
Berkhof, Johannes
van der Flier, Wiesje M.
author_sort van Maurik, Ingrid S.
collection PubMed
description INTRODUCTION: To construct a prognostic model based on amyloid positron emission tomography (PET) to predict clinical progression in individual patients with mild cognitive impairment (MCI). METHODS: We included 411 MCI patients from the Alzheimer's Disease Neuroimaging Initiative. Prognostic models were constructed with Cox regression with demographics, magnetic resonance imaging, and/or amyloid PET to predict progression to Alzheimer's disease dementia. The models were validated in the Amsterdam Dementia Cohort. RESULTS: The combined model (Harrell's C = 0.82 [0.78–0.86]) was significantly superior to demographics (β = 0.100, P < .001), magnetic resonance imaging (β = 0.037, P = .011), and PET only models (β = 0.053, P = .003).The models can be used to calculate individualized risk, for example, a female MCI patient (age = 60, APOE ε4 positive, Mini-Mental State Examination = 25, hippocampal volume = 5.8 cm(3), amyloid PET positive) has 35% (19–57) risk in one year and 85% (64–97) risk in three years. Model performances in the Amsterdam Dementia Cohort were reasonable. DISCUSSION: The present study facilitates the interpretation of an amyloid PET result in the context of a patient's own characteristics and clinical assessment.
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spelling pubmed-66677682019-08-06 Added value of amyloid PET in individualized risk predictions for MCI patients van Maurik, Ingrid S. van der Kall, Laura M. de Wilde, Arno Bouwman, Femke H. Scheltens, Philip van Berckel, Bart N.M. Berkhof, Johannes van der Flier, Wiesje M. Alzheimers Dement (Amst) Neuroimaging INTRODUCTION: To construct a prognostic model based on amyloid positron emission tomography (PET) to predict clinical progression in individual patients with mild cognitive impairment (MCI). METHODS: We included 411 MCI patients from the Alzheimer's Disease Neuroimaging Initiative. Prognostic models were constructed with Cox regression with demographics, magnetic resonance imaging, and/or amyloid PET to predict progression to Alzheimer's disease dementia. The models were validated in the Amsterdam Dementia Cohort. RESULTS: The combined model (Harrell's C = 0.82 [0.78–0.86]) was significantly superior to demographics (β = 0.100, P < .001), magnetic resonance imaging (β = 0.037, P = .011), and PET only models (β = 0.053, P = .003).The models can be used to calculate individualized risk, for example, a female MCI patient (age = 60, APOE ε4 positive, Mini-Mental State Examination = 25, hippocampal volume = 5.8 cm(3), amyloid PET positive) has 35% (19–57) risk in one year and 85% (64–97) risk in three years. Model performances in the Amsterdam Dementia Cohort were reasonable. DISCUSSION: The present study facilitates the interpretation of an amyloid PET result in the context of a patient's own characteristics and clinical assessment. Elsevier 2019-07-29 /pmc/articles/PMC6667768/ /pubmed/31388557 http://dx.doi.org/10.1016/j.dadm.2019.04.011 Text en © 2019 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Neuroimaging
van Maurik, Ingrid S.
van der Kall, Laura M.
de Wilde, Arno
Bouwman, Femke H.
Scheltens, Philip
van Berckel, Bart N.M.
Berkhof, Johannes
van der Flier, Wiesje M.
Added value of amyloid PET in individualized risk predictions for MCI patients
title Added value of amyloid PET in individualized risk predictions for MCI patients
title_full Added value of amyloid PET in individualized risk predictions for MCI patients
title_fullStr Added value of amyloid PET in individualized risk predictions for MCI patients
title_full_unstemmed Added value of amyloid PET in individualized risk predictions for MCI patients
title_short Added value of amyloid PET in individualized risk predictions for MCI patients
title_sort added value of amyloid pet in individualized risk predictions for mci patients
topic Neuroimaging
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6667768/
https://www.ncbi.nlm.nih.gov/pubmed/31388557
http://dx.doi.org/10.1016/j.dadm.2019.04.011
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