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A Longitudinal Study of Plasma pTau181 in Mild Cognitive Impairment with Lewy Bodies and Alzheimer's Disease

BACKGROUND: Alzheimer's disease (AD) co‐pathology is common in dementia with Lewy bodies and is associated with increased decline. Plasma pTau181 is a blood‐based biomarker that can detect AD co‐pathology. OBJECTIVES: We investigated whether pTau181 was associated with cognitive decline in mild...

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Autores principales: Thomas, Alan J., Hamilton, Calum A., Heslegrave, Amanda, Barker, Sally, Durcan, Rory, Lawley, Sarah, Barnett, Nicola, Lett, Debbie, Firbank, Michael, Roberts, Gemma, Taylor, John‐Paul, Donaghy, Paul C., Zetterberg, Henrik, O'Brien, John
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9540809/
https://www.ncbi.nlm.nih.gov/pubmed/35318733
http://dx.doi.org/10.1002/mds.28994
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author Thomas, Alan J.
Hamilton, Calum A.
Heslegrave, Amanda
Barker, Sally
Durcan, Rory
Lawley, Sarah
Barnett, Nicola
Lett, Debbie
Firbank, Michael
Roberts, Gemma
Taylor, John‐Paul
Donaghy, Paul C.
Zetterberg, Henrik
O'Brien, John
author_facet Thomas, Alan J.
Hamilton, Calum A.
Heslegrave, Amanda
Barker, Sally
Durcan, Rory
Lawley, Sarah
Barnett, Nicola
Lett, Debbie
Firbank, Michael
Roberts, Gemma
Taylor, John‐Paul
Donaghy, Paul C.
Zetterberg, Henrik
O'Brien, John
author_sort Thomas, Alan J.
collection PubMed
description BACKGROUND: Alzheimer's disease (AD) co‐pathology is common in dementia with Lewy bodies and is associated with increased decline. Plasma pTau181 is a blood‐based biomarker that can detect AD co‐pathology. OBJECTIVES: We investigated whether pTau181 was associated with cognitive decline in mild cognitive impairment with Lewy bodies (MCI‐LB) and MCI with AD (MCI‐AD). METHODS: We assessed plasma pTau181 using a single‐molecule array (Simoa) immunoassay at baseline and follow‐up in a longitudinal cohort of MCI‐LB, MCI‐AD, and controls. RESULTS: One hundred forty‐six subjects (56 probable MCI‐LB, 22 possible MCI‐LB, 44 MCI‐AD, and 24 controls) were reviewed for up to 5.7 years. Probable MCI‐LB had significantly higher pTau181 (22.2% mean increase) compared with controls and significantly lower (24.4% mean decrease) levels compared with MCI‐AD. Receiver operating characteristic analyses of pTau181 in discriminating probable MCI‐LB from controls showed an area under the curve (AUC) of 0.68 (83% specificity, 57% sensitivity); for discriminating MCI‐AD from healthy controls, AUC was 0.8 (83.3% specificity, 72.7% sensitivity). pTau181 concentration was less useful in discriminating between probable MCI‐LB and MCI‐AD: AUC of 0.64 (71.4% specificity, 52.3% sensitivity). There was an association between pTau181 and cognitive decline in MCI‐AD but not in MCI‐LB. In a subset with repeat samples there was a nonsignificant 3% increase per follow‐up year in plasma pTau181. The rate of change in pTau181 was not significantly different in different diagnostic subgroups. CONCLUSIONS: pTau181 was not associated with an increased decline assessed using either baseline or repeat pTau181. pTau181 partially discriminated probable MCI‐LB from controls and MCI‐AD from controls but was not useful in distinguishing probable MCI‐LB from MCI‐AD. © 2022 The Authors. Movement Disorders published by Wiley Periodicals LLC on behalf of International Parkinson and Movement Disorder Society
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spelling pubmed-95408092022-10-14 A Longitudinal Study of Plasma pTau181 in Mild Cognitive Impairment with Lewy Bodies and Alzheimer's Disease Thomas, Alan J. Hamilton, Calum A. Heslegrave, Amanda Barker, Sally Durcan, Rory Lawley, Sarah Barnett, Nicola Lett, Debbie Firbank, Michael Roberts, Gemma Taylor, John‐Paul Donaghy, Paul C. Zetterberg, Henrik O'Brien, John Mov Disord Regular Issue Articles BACKGROUND: Alzheimer's disease (AD) co‐pathology is common in dementia with Lewy bodies and is associated with increased decline. Plasma pTau181 is a blood‐based biomarker that can detect AD co‐pathology. OBJECTIVES: We investigated whether pTau181 was associated with cognitive decline in mild cognitive impairment with Lewy bodies (MCI‐LB) and MCI with AD (MCI‐AD). METHODS: We assessed plasma pTau181 using a single‐molecule array (Simoa) immunoassay at baseline and follow‐up in a longitudinal cohort of MCI‐LB, MCI‐AD, and controls. RESULTS: One hundred forty‐six subjects (56 probable MCI‐LB, 22 possible MCI‐LB, 44 MCI‐AD, and 24 controls) were reviewed for up to 5.7 years. Probable MCI‐LB had significantly higher pTau181 (22.2% mean increase) compared with controls and significantly lower (24.4% mean decrease) levels compared with MCI‐AD. Receiver operating characteristic analyses of pTau181 in discriminating probable MCI‐LB from controls showed an area under the curve (AUC) of 0.68 (83% specificity, 57% sensitivity); for discriminating MCI‐AD from healthy controls, AUC was 0.8 (83.3% specificity, 72.7% sensitivity). pTau181 concentration was less useful in discriminating between probable MCI‐LB and MCI‐AD: AUC of 0.64 (71.4% specificity, 52.3% sensitivity). There was an association between pTau181 and cognitive decline in MCI‐AD but not in MCI‐LB. In a subset with repeat samples there was a nonsignificant 3% increase per follow‐up year in plasma pTau181. The rate of change in pTau181 was not significantly different in different diagnostic subgroups. CONCLUSIONS: pTau181 was not associated with an increased decline assessed using either baseline or repeat pTau181. pTau181 partially discriminated probable MCI‐LB from controls and MCI‐AD from controls but was not useful in distinguishing probable MCI‐LB from MCI‐AD. © 2022 The Authors. Movement Disorders published by Wiley Periodicals LLC on behalf of International Parkinson and Movement Disorder Society John Wiley & Sons, Inc. 2022-03-23 2022-07 /pmc/articles/PMC9540809/ /pubmed/35318733 http://dx.doi.org/10.1002/mds.28994 Text en © 2022 The Authors. Movement Disorders published by Wiley Periodicals LLC on behalf of International Parkinson and Movement Disorder Society 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 Regular Issue Articles
Thomas, Alan J.
Hamilton, Calum A.
Heslegrave, Amanda
Barker, Sally
Durcan, Rory
Lawley, Sarah
Barnett, Nicola
Lett, Debbie
Firbank, Michael
Roberts, Gemma
Taylor, John‐Paul
Donaghy, Paul C.
Zetterberg, Henrik
O'Brien, John
A Longitudinal Study of Plasma pTau181 in Mild Cognitive Impairment with Lewy Bodies and Alzheimer's Disease
title A Longitudinal Study of Plasma pTau181 in Mild Cognitive Impairment with Lewy Bodies and Alzheimer's Disease
title_full A Longitudinal Study of Plasma pTau181 in Mild Cognitive Impairment with Lewy Bodies and Alzheimer's Disease
title_fullStr A Longitudinal Study of Plasma pTau181 in Mild Cognitive Impairment with Lewy Bodies and Alzheimer's Disease
title_full_unstemmed A Longitudinal Study of Plasma pTau181 in Mild Cognitive Impairment with Lewy Bodies and Alzheimer's Disease
title_short A Longitudinal Study of Plasma pTau181 in Mild Cognitive Impairment with Lewy Bodies and Alzheimer's Disease
title_sort longitudinal study of plasma ptau181 in mild cognitive impairment with lewy bodies and alzheimer's disease
topic Regular Issue Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9540809/
https://www.ncbi.nlm.nih.gov/pubmed/35318733
http://dx.doi.org/10.1002/mds.28994
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