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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...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
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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. |
format | Online Article Text |
id | pubmed-9249966 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
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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