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Plasma p217+tau versus NAV4694 amyloid and MK6240 tau PET across the Alzheimer's continuum
INTRODUCTION: We evaluated a new Simoa plasma assay for phosphorylated tau (P‐tau) at aa217 enhanced by additional p‐tau sites (p217+tau). METHODS: Plasma p217+tau levels were compared to (18)F‐NAV4694 amyloid beta (Aβ) positron emission tomography (PET) and (18)F‐MK6240 tau PET in 174 cognitively i...
Autores principales: | , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8984092/ https://www.ncbi.nlm.nih.gov/pubmed/35415202 http://dx.doi.org/10.1002/dad2.12307 |
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author | Doré, Vincent Doecke, James D. Saad, Ziad S. Triana‐Baltzer, Gallen Slemmon, Randy Krishnadas, Natasha Bourgeat, Pierrick Huang, Kun Burnham, Samantha Fowler, Christopher Rainey‐Smith, Stephanie R. Bush, Ashley I. Ward, Larry Robertson, Jo Martins, Ralph N. Masters, Colin L. Villemagne, Victor L. Fripp, Jurgen Kolb, Hartmuth C. Rowe, Christopher C. |
author_facet | Doré, Vincent Doecke, James D. Saad, Ziad S. Triana‐Baltzer, Gallen Slemmon, Randy Krishnadas, Natasha Bourgeat, Pierrick Huang, Kun Burnham, Samantha Fowler, Christopher Rainey‐Smith, Stephanie R. Bush, Ashley I. Ward, Larry Robertson, Jo Martins, Ralph N. Masters, Colin L. Villemagne, Victor L. Fripp, Jurgen Kolb, Hartmuth C. Rowe, Christopher C. |
author_sort | Doré, Vincent |
collection | PubMed |
description | INTRODUCTION: We evaluated a new Simoa plasma assay for phosphorylated tau (P‐tau) at aa217 enhanced by additional p‐tau sites (p217+tau). METHODS: Plasma p217+tau levels were compared to (18)F‐NAV4694 amyloid beta (Aβ) positron emission tomography (PET) and (18)F‐MK6240 tau PET in 174 cognitively impaired (CI) and 223 cognitively unimpaired (CU) participants. RESULTS: Compared to Aβ− CU, the plasma levels of p217+tau increased 2‐fold in Aβ+ CU and 3.5‐fold in Aβ+ CI. In Aβ− the p217+tau levels did not differ significantly between CU and CI. P217+tau correlated with Aβ centiloids P = .67 (CI, P = .64; CU, P = .45) and tau SUVR(MT) P = .63 (CI, P = .69; CU, P = .34). Area under curve (AUC) for Alzheimer's disease (AD) dementia versus Aβ− CU was 0.94, for AD dementia versus other dementia was 0.93, for Aβ+ versus Aβ− PET was 0.89, and for tau+ versus tau− PET was 0.89. DISCUSSION: Plasma p217+tau levels elevate early in the AD continuum and correlate well with Aβ and tau PET. |
format | Online Article Text |
id | pubmed-8984092 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-89840922022-04-11 Plasma p217+tau versus NAV4694 amyloid and MK6240 tau PET across the Alzheimer's continuum Doré, Vincent Doecke, James D. Saad, Ziad S. Triana‐Baltzer, Gallen Slemmon, Randy Krishnadas, Natasha Bourgeat, Pierrick Huang, Kun Burnham, Samantha Fowler, Christopher Rainey‐Smith, Stephanie R. Bush, Ashley I. Ward, Larry Robertson, Jo Martins, Ralph N. Masters, Colin L. Villemagne, Victor L. Fripp, Jurgen Kolb, Hartmuth C. Rowe, Christopher C. Alzheimers Dement (Amst) Research Articles INTRODUCTION: We evaluated a new Simoa plasma assay for phosphorylated tau (P‐tau) at aa217 enhanced by additional p‐tau sites (p217+tau). METHODS: Plasma p217+tau levels were compared to (18)F‐NAV4694 amyloid beta (Aβ) positron emission tomography (PET) and (18)F‐MK6240 tau PET in 174 cognitively impaired (CI) and 223 cognitively unimpaired (CU) participants. RESULTS: Compared to Aβ− CU, the plasma levels of p217+tau increased 2‐fold in Aβ+ CU and 3.5‐fold in Aβ+ CI. In Aβ− the p217+tau levels did not differ significantly between CU and CI. P217+tau correlated with Aβ centiloids P = .67 (CI, P = .64; CU, P = .45) and tau SUVR(MT) P = .63 (CI, P = .69; CU, P = .34). Area under curve (AUC) for Alzheimer's disease (AD) dementia versus Aβ− CU was 0.94, for AD dementia versus other dementia was 0.93, for Aβ+ versus Aβ− PET was 0.89, and for tau+ versus tau− PET was 0.89. DISCUSSION: Plasma p217+tau levels elevate early in the AD continuum and correlate well with Aβ and tau PET. John Wiley and Sons Inc. 2022-04-05 /pmc/articles/PMC8984092/ /pubmed/35415202 http://dx.doi.org/10.1002/dad2.12307 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-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Research Articles Doré, Vincent Doecke, James D. Saad, Ziad S. Triana‐Baltzer, Gallen Slemmon, Randy Krishnadas, Natasha Bourgeat, Pierrick Huang, Kun Burnham, Samantha Fowler, Christopher Rainey‐Smith, Stephanie R. Bush, Ashley I. Ward, Larry Robertson, Jo Martins, Ralph N. Masters, Colin L. Villemagne, Victor L. Fripp, Jurgen Kolb, Hartmuth C. Rowe, Christopher C. Plasma p217+tau versus NAV4694 amyloid and MK6240 tau PET across the Alzheimer's continuum |
title | Plasma p217+tau versus NAV4694 amyloid and MK6240 tau PET across the Alzheimer's continuum |
title_full | Plasma p217+tau versus NAV4694 amyloid and MK6240 tau PET across the Alzheimer's continuum |
title_fullStr | Plasma p217+tau versus NAV4694 amyloid and MK6240 tau PET across the Alzheimer's continuum |
title_full_unstemmed | Plasma p217+tau versus NAV4694 amyloid and MK6240 tau PET across the Alzheimer's continuum |
title_short | Plasma p217+tau versus NAV4694 amyloid and MK6240 tau PET across the Alzheimer's continuum |
title_sort | plasma p217+tau versus nav4694 amyloid and mk6240 tau pet across the alzheimer's continuum |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8984092/ https://www.ncbi.nlm.nih.gov/pubmed/35415202 http://dx.doi.org/10.1002/dad2.12307 |
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