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Cerebrospinal fluid levels of fatty acid–binding protein 3 are associated with likelihood of amyloidopathy in cognitively healthy individuals

INTRODUCTION: Fatty acid–binding protein 3 (FABP3) is a biomarker of neuronal membrane disruption, associated with lipid dyshomeostasis—a notable Alzheimer's disease (AD) pathophysiological change. We assessed the association of cerebrospinal fluid (CSF) FABP3 levels with brain amyloidosis and...

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Autores principales: Dhiman, Kunal, Villemagne, Victor L., Fowler, Christopher, Bourgeat, Pierrick, Li, Qiao‐Xin, Collins, Steven, Rowe, Christopher C., Masters, Colin L., Ames, David, Blennow, Kaj, Zetterberg, Henrik, Martins, Ralph N., Gupta, Veer
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9719998/
https://www.ncbi.nlm.nih.gov/pubmed/36479019
http://dx.doi.org/10.1002/dad2.12377
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author Dhiman, Kunal
Villemagne, Victor L.
Fowler, Christopher
Bourgeat, Pierrick
Li, Qiao‐Xin
Collins, Steven
Rowe, Christopher C.
Masters, Colin L.
Ames, David
Blennow, Kaj
Zetterberg, Henrik
Martins, Ralph N.
Gupta, Veer
author_facet Dhiman, Kunal
Villemagne, Victor L.
Fowler, Christopher
Bourgeat, Pierrick
Li, Qiao‐Xin
Collins, Steven
Rowe, Christopher C.
Masters, Colin L.
Ames, David
Blennow, Kaj
Zetterberg, Henrik
Martins, Ralph N.
Gupta, Veer
author_sort Dhiman, Kunal
collection PubMed
description INTRODUCTION: Fatty acid–binding protein 3 (FABP3) is a biomarker of neuronal membrane disruption, associated with lipid dyshomeostasis—a notable Alzheimer's disease (AD) pathophysiological change. We assessed the association of cerebrospinal fluid (CSF) FABP3 levels with brain amyloidosis and the likelihood/risk of developing amyloidopathy in cognitively healthy individuals. METHODS: FABP3 levels were measured in CSF samples of cognitively healthy participants, > 60 years of age (n = 142), from the Australian Imaging, Biomarkers & Lifestyle Flagship Study of Ageing (AIBL). RESULTS: FABP3 levels were positively associated with baseline brain amyloid beta (Aβ) load as measured by standardized uptake value ratio (SUVR, standardized β = 0.22, P = .009) and predicted the change in brain Aβ load (standardized β = 0.32, P = .004). Higher levels of CSF FABP3 (above median) were associated with a likelihood of amyloidopathy (odds ratio [OR] 2.28, 95% confidence interval [CI] 1.12 to 4.65, P = .023). DISCUSSION: These results support inclusion of CSF FABP3 as a biomarker in risk‐prediction models of AD.
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spelling pubmed-97199982022-12-06 Cerebrospinal fluid levels of fatty acid–binding protein 3 are associated with likelihood of amyloidopathy in cognitively healthy individuals Dhiman, Kunal Villemagne, Victor L. Fowler, Christopher Bourgeat, Pierrick Li, Qiao‐Xin Collins, Steven Rowe, Christopher C. Masters, Colin L. Ames, David Blennow, Kaj Zetterberg, Henrik Martins, Ralph N. Gupta, Veer Alzheimers Dement (Amst) Research Articles INTRODUCTION: Fatty acid–binding protein 3 (FABP3) is a biomarker of neuronal membrane disruption, associated with lipid dyshomeostasis—a notable Alzheimer's disease (AD) pathophysiological change. We assessed the association of cerebrospinal fluid (CSF) FABP3 levels with brain amyloidosis and the likelihood/risk of developing amyloidopathy in cognitively healthy individuals. METHODS: FABP3 levels were measured in CSF samples of cognitively healthy participants, > 60 years of age (n = 142), from the Australian Imaging, Biomarkers & Lifestyle Flagship Study of Ageing (AIBL). RESULTS: FABP3 levels were positively associated with baseline brain amyloid beta (Aβ) load as measured by standardized uptake value ratio (SUVR, standardized β = 0.22, P = .009) and predicted the change in brain Aβ load (standardized β = 0.32, P = .004). Higher levels of CSF FABP3 (above median) were associated with a likelihood of amyloidopathy (odds ratio [OR] 2.28, 95% confidence interval [CI] 1.12 to 4.65, P = .023). DISCUSSION: These results support inclusion of CSF FABP3 as a biomarker in risk‐prediction models of AD. John Wiley and Sons Inc. 2022-12-04 /pmc/articles/PMC9719998/ /pubmed/36479019 http://dx.doi.org/10.1002/dad2.12377 Text en © 2022 The Authors. Alzheimer's & Dementia: Diagnosis, Assessment & Disease Monitoring published by Wiley Periodicals, LLC on behalf of Alzheimer's Association. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Research Articles
Dhiman, Kunal
Villemagne, Victor L.
Fowler, Christopher
Bourgeat, Pierrick
Li, Qiao‐Xin
Collins, Steven
Rowe, Christopher C.
Masters, Colin L.
Ames, David
Blennow, Kaj
Zetterberg, Henrik
Martins, Ralph N.
Gupta, Veer
Cerebrospinal fluid levels of fatty acid–binding protein 3 are associated with likelihood of amyloidopathy in cognitively healthy individuals
title Cerebrospinal fluid levels of fatty acid–binding protein 3 are associated with likelihood of amyloidopathy in cognitively healthy individuals
title_full Cerebrospinal fluid levels of fatty acid–binding protein 3 are associated with likelihood of amyloidopathy in cognitively healthy individuals
title_fullStr Cerebrospinal fluid levels of fatty acid–binding protein 3 are associated with likelihood of amyloidopathy in cognitively healthy individuals
title_full_unstemmed Cerebrospinal fluid levels of fatty acid–binding protein 3 are associated with likelihood of amyloidopathy in cognitively healthy individuals
title_short Cerebrospinal fluid levels of fatty acid–binding protein 3 are associated with likelihood of amyloidopathy in cognitively healthy individuals
title_sort cerebrospinal fluid levels of fatty acid–binding protein 3 are associated with likelihood of amyloidopathy in cognitively healthy individuals
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9719998/
https://www.ncbi.nlm.nih.gov/pubmed/36479019
http://dx.doi.org/10.1002/dad2.12377
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