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Longitudinal CSF proteomics identifies NPTX2 as a prognostic biomarker of Alzheimer's disease

Introduction: Biomarkers that reflect pathologic processes affecting neuronal function during preclinical and early stages of Alzheimer's disease (AD) are needed to aid drug development. Methods: A targeted, stable isotope, quantitative mass spectrometry‐based investigation of longitudinal chan...

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Autores principales: Libiger, Ondrej, Shaw, Leslie M., Watson, Mark H., Nairn, Angus C., Umaña, Kelly L., Biarnes, Michael C., Canet‐Avilés, Rosa M., Jack, Clifford R., Breton, Yannick‐André, Cortes, Laetitia, Chelsky, Daniel, Spellman, Daniel S., Baker, Susan A., Raghavan, Nandini, Potter, William Z.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9222372/
https://www.ncbi.nlm.nih.gov/pubmed/33984181
http://dx.doi.org/10.1002/alz.12353
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author Libiger, Ondrej
Shaw, Leslie M.
Watson, Mark H.
Nairn, Angus C.
Umaña, Kelly L.
Biarnes, Michael C.
Canet‐Avilés, Rosa M.
Jack, Clifford R.
Breton, Yannick‐André
Cortes, Laetitia
Chelsky, Daniel
Spellman, Daniel S.
Baker, Susan A.
Raghavan, Nandini
Potter, William Z.
author_facet Libiger, Ondrej
Shaw, Leslie M.
Watson, Mark H.
Nairn, Angus C.
Umaña, Kelly L.
Biarnes, Michael C.
Canet‐Avilés, Rosa M.
Jack, Clifford R.
Breton, Yannick‐André
Cortes, Laetitia
Chelsky, Daniel
Spellman, Daniel S.
Baker, Susan A.
Raghavan, Nandini
Potter, William Z.
author_sort Libiger, Ondrej
collection PubMed
description Introduction: Biomarkers that reflect pathologic processes affecting neuronal function during preclinical and early stages of Alzheimer's disease (AD) are needed to aid drug development. Methods: A targeted, stable isotope, quantitative mass spectrometry‐based investigation of longitudinal changes in concentrations of previously identified candidate biomarkers was performed in cerebrospinal fluid (CSF) of Alzheimer's Disease Neuroimaging Initiative participants who were classified as cognitively normal (CN; n = 76) or with mild cognitive impairment (MCI; n = 111) at baseline. Results: Of the candidate biomarkers, the CSF concentration of neuronal pentraxin 2 (NPTX2), a protein involved in synaptic function, exhibited rates of change that were significantly different between three comparison groups (i.e., CN vs. MCI participants; AD pathology positive vs. negative defined by phosphorylated tau181/amyloid beta1‐42 ratio; and clinical progressors vs. non‐progressors). The rate of change of NPTX2 also significantly correlated with declining cognition. Discussion: CSF NPTX2 concentration is a strong prognostic biomarker candidate of accelerated cognitive decline with potential use as a therapeutic target.
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spelling pubmed-92223722022-06-23 Longitudinal CSF proteomics identifies NPTX2 as a prognostic biomarker of Alzheimer's disease Libiger, Ondrej Shaw, Leslie M. Watson, Mark H. Nairn, Angus C. Umaña, Kelly L. Biarnes, Michael C. Canet‐Avilés, Rosa M. Jack, Clifford R. Breton, Yannick‐André Cortes, Laetitia Chelsky, Daniel Spellman, Daniel S. Baker, Susan A. Raghavan, Nandini Potter, William Z. Alzheimers Dement Featured Articles Introduction: Biomarkers that reflect pathologic processes affecting neuronal function during preclinical and early stages of Alzheimer's disease (AD) are needed to aid drug development. Methods: A targeted, stable isotope, quantitative mass spectrometry‐based investigation of longitudinal changes in concentrations of previously identified candidate biomarkers was performed in cerebrospinal fluid (CSF) of Alzheimer's Disease Neuroimaging Initiative participants who were classified as cognitively normal (CN; n = 76) or with mild cognitive impairment (MCI; n = 111) at baseline. Results: Of the candidate biomarkers, the CSF concentration of neuronal pentraxin 2 (NPTX2), a protein involved in synaptic function, exhibited rates of change that were significantly different between three comparison groups (i.e., CN vs. MCI participants; AD pathology positive vs. negative defined by phosphorylated tau181/amyloid beta1‐42 ratio; and clinical progressors vs. non‐progressors). The rate of change of NPTX2 also significantly correlated with declining cognition. Discussion: CSF NPTX2 concentration is a strong prognostic biomarker candidate of accelerated cognitive decline with potential use as a therapeutic target. John Wiley and Sons Inc. 2021-05-13 2021-12 /pmc/articles/PMC9222372/ /pubmed/33984181 http://dx.doi.org/10.1002/alz.12353 Text en © 2021 The Authors. Alzheimer's & Dementia 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 Featured Articles
Libiger, Ondrej
Shaw, Leslie M.
Watson, Mark H.
Nairn, Angus C.
Umaña, Kelly L.
Biarnes, Michael C.
Canet‐Avilés, Rosa M.
Jack, Clifford R.
Breton, Yannick‐André
Cortes, Laetitia
Chelsky, Daniel
Spellman, Daniel S.
Baker, Susan A.
Raghavan, Nandini
Potter, William Z.
Longitudinal CSF proteomics identifies NPTX2 as a prognostic biomarker of Alzheimer's disease
title Longitudinal CSF proteomics identifies NPTX2 as a prognostic biomarker of Alzheimer's disease
title_full Longitudinal CSF proteomics identifies NPTX2 as a prognostic biomarker of Alzheimer's disease
title_fullStr Longitudinal CSF proteomics identifies NPTX2 as a prognostic biomarker of Alzheimer's disease
title_full_unstemmed Longitudinal CSF proteomics identifies NPTX2 as a prognostic biomarker of Alzheimer's disease
title_short Longitudinal CSF proteomics identifies NPTX2 as a prognostic biomarker of Alzheimer's disease
title_sort longitudinal csf proteomics identifies nptx2 as a prognostic biomarker of alzheimer's disease
topic Featured Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9222372/
https://www.ncbi.nlm.nih.gov/pubmed/33984181
http://dx.doi.org/10.1002/alz.12353
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