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Detection of Alzheimer's disease amyloid beta 1‐42, p‐tau, and t‐tau assays

INTRODUCTION: We aimed to provide cut points for the automated Elecsys Alzheimer's disease (AD) cerebrospinal fluid (CSF) biomarkers. METHODS: Cut points for Elecsys amyloid beta 42 (Aβ42), total tau (t‐tau), hyperphosphorylated tau (p‐tau), and t‐tau/Aβ42 and p‐tau/Aβ42 ratios were evaluated i...

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Autores principales: van Harten, Argonde C., Wiste, Heather J., Weigand, Stephen D., Mielke, Michelle M., Kremers, Walter K., Eichenlaub, Udo, Dyer, Roy B., Algeciras‐Schimnich, Alicia, Knopman, David S., Jack, Clifford R., Petersen, Ronald C.
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/PMC9249966/
https://www.ncbi.nlm.nih.gov/pubmed/34310035
http://dx.doi.org/10.1002/alz.12406
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author van Harten, Argonde C.
Wiste, Heather J.
Weigand, Stephen D.
Mielke, Michelle M.
Kremers, Walter K.
Eichenlaub, Udo
Dyer, Roy B.
Algeciras‐Schimnich, Alicia
Knopman, David S.
Jack, Clifford R.
Petersen, Ronald C.
author_facet van Harten, Argonde C.
Wiste, Heather J.
Weigand, Stephen D.
Mielke, Michelle M.
Kremers, Walter K.
Eichenlaub, Udo
Dyer, Roy B.
Algeciras‐Schimnich, Alicia
Knopman, David S.
Jack, Clifford R.
Petersen, Ronald C.
author_sort van Harten, Argonde C.
collection PubMed
description INTRODUCTION: We aimed to provide cut points for the automated Elecsys Alzheimer's disease (AD) cerebrospinal fluid (CSF) biomarkers. METHODS: Cut points for Elecsys amyloid beta 42 (Aβ42), total tau (t‐tau), hyperphosphorylated tau (p‐tau), and t‐tau/Aβ42 and p‐tau/Aβ42 ratios were evaluated in Mayo Clinic Study of Aging (n = 804) and Mayo Clinic Alzheimer's Disease Research Center (n = 70) participants. RESULTS: The t‐tau/Aβ42 and p‐tau/Aβ42 ratios had a higher percent agreement with normal/abnormal amyloid positron emission tomography (PET) than the individual CSF markers. Reciever Operating Characteristic (ROC)‐based cut points were 0.26 (0.24–0.27) for t‐tau/Aβ42 and 0.023 (0.020–0.025) for p‐tau/Aβ42. Ratio cut points derived from other cohorts performed as well in our cohort as our own did. Individual biomarkers had worse diagnostic properties and more variable results in terms of positive and negative percent agreement (PPA and NPA). CONCLUSION: CSF t‐tau/Aβ42 and p‐tau/Aβ42 ratios are very robust indicators of AD. For individual biomarkers, the intended use should determine which cut point is chosen.
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spelling pubmed-92499662022-10-14 Detection of Alzheimer's disease amyloid beta 1‐42, p‐tau, and t‐tau assays van Harten, Argonde C. Wiste, Heather J. Weigand, Stephen D. Mielke, Michelle M. Kremers, Walter K. Eichenlaub, Udo Dyer, Roy B. Algeciras‐Schimnich, Alicia Knopman, David S. Jack, Clifford R. Petersen, Ronald C. Alzheimers Dement Featured Articles INTRODUCTION: We aimed to provide cut points for the automated Elecsys Alzheimer's disease (AD) cerebrospinal fluid (CSF) biomarkers. METHODS: Cut points for Elecsys amyloid beta 42 (Aβ42), total tau (t‐tau), hyperphosphorylated tau (p‐tau), and t‐tau/Aβ42 and p‐tau/Aβ42 ratios were evaluated in Mayo Clinic Study of Aging (n = 804) and Mayo Clinic Alzheimer's Disease Research Center (n = 70) participants. RESULTS: The t‐tau/Aβ42 and p‐tau/Aβ42 ratios had a higher percent agreement with normal/abnormal amyloid positron emission tomography (PET) than the individual CSF markers. Reciever Operating Characteristic (ROC)‐based cut points were 0.26 (0.24–0.27) for t‐tau/Aβ42 and 0.023 (0.020–0.025) for p‐tau/Aβ42. Ratio cut points derived from other cohorts performed as well in our cohort as our own did. Individual biomarkers had worse diagnostic properties and more variable results in terms of positive and negative percent agreement (PPA and NPA). CONCLUSION: CSF t‐tau/Aβ42 and p‐tau/Aβ42 ratios are very robust indicators of AD. For individual biomarkers, the intended use should determine which cut point is chosen. John Wiley and Sons Inc. 2021-07-26 2022-04 /pmc/articles/PMC9249966/ /pubmed/34310035 http://dx.doi.org/10.1002/alz.12406 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
van Harten, Argonde C.
Wiste, Heather J.
Weigand, Stephen D.
Mielke, Michelle M.
Kremers, Walter K.
Eichenlaub, Udo
Dyer, Roy B.
Algeciras‐Schimnich, Alicia
Knopman, David S.
Jack, Clifford R.
Petersen, Ronald C.
Detection of Alzheimer's disease amyloid beta 1‐42, p‐tau, and t‐tau assays
title Detection of Alzheimer's disease amyloid beta 1‐42, p‐tau, and t‐tau assays
title_full Detection of Alzheimer's disease amyloid beta 1‐42, p‐tau, and t‐tau assays
title_fullStr Detection of Alzheimer's disease amyloid beta 1‐42, p‐tau, and t‐tau assays
title_full_unstemmed Detection of Alzheimer's disease amyloid beta 1‐42, p‐tau, and t‐tau assays
title_short Detection of Alzheimer's disease amyloid beta 1‐42, p‐tau, and t‐tau assays
title_sort detection of alzheimer's disease amyloid beta 1‐42, p‐tau, and t‐tau assays
topic Featured Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9249966/
https://www.ncbi.nlm.nih.gov/pubmed/34310035
http://dx.doi.org/10.1002/alz.12406
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