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Comparing tau status determined via plasma pTau181, pTau231 and [(18)F]MK6240 tau-PET

BACKGROUND: Tau in Alzheimer's disease (AD) is assessed via cerebrospinal fluid (CSF) and Positron emission tomography (PET). Novel methods to detect phosphorylated tau (pTau) in blood have been recently developed. We aim to investigate agreement of tau status as determined by [(18)F]MK6240 tau...

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Autores principales: Tissot, Cécile, Therriault, Joseph, Kunach, Peter, L Benedet, Andréa, Pascoal, Tharick A., Ashton, Nicholas J., Karikari, Thomas K., Servaes, Stijn, Lussier, Firoza Z., Chamoun, Mira, Tudorascu, Dana L., Stevenson, Jenna, Rahmouni, Nesrine, Poltronetti, Nina Margherita, Pallen, Vanessa, Bezgin, Gleb, Kang, Min Su, Mathotaarachchi, Sulantha S., Wang, Yi-Ting, Fernandez Arias, Jaime, Ferreira, Pamela Cristina Lukasewicz, Ferrari-Souza, João Pedro, Vanmechelen, Eugeen, Blennow, Kaj, Zetterberg, Henrik, Gauthier, Serge, Rosa-Neto, Pedro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8844756/
https://www.ncbi.nlm.nih.gov/pubmed/35134647
http://dx.doi.org/10.1016/j.ebiom.2022.103837
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author Tissot, Cécile
Therriault, Joseph
Kunach, Peter
L Benedet, Andréa
Pascoal, Tharick A.
Ashton, Nicholas J.
Karikari, Thomas K.
Servaes, Stijn
Lussier, Firoza Z.
Chamoun, Mira
Tudorascu, Dana L.
Stevenson, Jenna
Rahmouni, Nesrine
Poltronetti, Nina Margherita
Pallen, Vanessa
Bezgin, Gleb
Kang, Min Su
Mathotaarachchi, Sulantha S.
Wang, Yi-Ting
Fernandez Arias, Jaime
Ferreira, Pamela Cristina Lukasewicz
Ferrari-Souza, João Pedro
Vanmechelen, Eugeen
Blennow, Kaj
Zetterberg, Henrik
Gauthier, Serge
Rosa-Neto, Pedro
author_facet Tissot, Cécile
Therriault, Joseph
Kunach, Peter
L Benedet, Andréa
Pascoal, Tharick A.
Ashton, Nicholas J.
Karikari, Thomas K.
Servaes, Stijn
Lussier, Firoza Z.
Chamoun, Mira
Tudorascu, Dana L.
Stevenson, Jenna
Rahmouni, Nesrine
Poltronetti, Nina Margherita
Pallen, Vanessa
Bezgin, Gleb
Kang, Min Su
Mathotaarachchi, Sulantha S.
Wang, Yi-Ting
Fernandez Arias, Jaime
Ferreira, Pamela Cristina Lukasewicz
Ferrari-Souza, João Pedro
Vanmechelen, Eugeen
Blennow, Kaj
Zetterberg, Henrik
Gauthier, Serge
Rosa-Neto, Pedro
author_sort Tissot, Cécile
collection PubMed
description BACKGROUND: Tau in Alzheimer's disease (AD) is assessed via cerebrospinal fluid (CSF) and Positron emission tomography (PET). Novel methods to detect phosphorylated tau (pTau) in blood have been recently developed. We aim to investigate agreement of tau status as determined by [(18)F]MK6240 tau-PET, plasma pTau181 and pTau231. METHODS: We assessed cognitively unimpaired young, cognitively unimpaired, mild cognitive impairment and AD individuals with [(18)F]MK6240, plasma pTau181, pTau 231, [(18)F]AZD4694 amyloid-PET and MRI. A subset underwent CSF assessment. We conducted ROC curves to obtain cut-off values for plasma pTau epitopes. Individuals were categorized as positive or negative in all biomarkers. We then compared the distribution among concordant and discordant groups in relation to diagnosis, Aβ status, APOEε4 status, [(18)F]AZD4694 global SUVR, hippocampal volume and CSF pTau181. FINDINGS: The threshold for positivity was 15.085 pg/mL for plasma pTau181 and 17.652 pg/mL for plasma pTau231. Most individuals had concordant statuses, however, 18% of plasma181/PET, 26% of plasma231/PET and 25% of the pTau231/pTau181 were discordant. Positivity to at least one biomarker was often accompanied by diagnosis of cognitive impairment, Aβ positivity, APOEε4 carriership, higher levels of [(18)F]AZD4694 global SUVR, hippocampal atrophy and CSF pTau181. INTERPRETATION: Plasma pTau181, pTau231 and [(18)F]MK6240 seem to reflect different stages of tau progression. Plasma biomarkers can be useful in the context of diagnostic information and clinical trials, to evaluate the disease stage. Moreover, they seem to confidently evaluate tau-PET positivity. FUNDING: Moreover, this study was supported by Weston Brain Institute, Canadian Institute of Health Research and Fonds de Recherche du Québec.
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spelling pubmed-88447562022-02-22 Comparing tau status determined via plasma pTau181, pTau231 and [(18)F]MK6240 tau-PET Tissot, Cécile Therriault, Joseph Kunach, Peter L Benedet, Andréa Pascoal, Tharick A. Ashton, Nicholas J. Karikari, Thomas K. Servaes, Stijn Lussier, Firoza Z. Chamoun, Mira Tudorascu, Dana L. Stevenson, Jenna Rahmouni, Nesrine Poltronetti, Nina Margherita Pallen, Vanessa Bezgin, Gleb Kang, Min Su Mathotaarachchi, Sulantha S. Wang, Yi-Ting Fernandez Arias, Jaime Ferreira, Pamela Cristina Lukasewicz Ferrari-Souza, João Pedro Vanmechelen, Eugeen Blennow, Kaj Zetterberg, Henrik Gauthier, Serge Rosa-Neto, Pedro EBioMedicine Articles BACKGROUND: Tau in Alzheimer's disease (AD) is assessed via cerebrospinal fluid (CSF) and Positron emission tomography (PET). Novel methods to detect phosphorylated tau (pTau) in blood have been recently developed. We aim to investigate agreement of tau status as determined by [(18)F]MK6240 tau-PET, plasma pTau181 and pTau231. METHODS: We assessed cognitively unimpaired young, cognitively unimpaired, mild cognitive impairment and AD individuals with [(18)F]MK6240, plasma pTau181, pTau 231, [(18)F]AZD4694 amyloid-PET and MRI. A subset underwent CSF assessment. We conducted ROC curves to obtain cut-off values for plasma pTau epitopes. Individuals were categorized as positive or negative in all biomarkers. We then compared the distribution among concordant and discordant groups in relation to diagnosis, Aβ status, APOEε4 status, [(18)F]AZD4694 global SUVR, hippocampal volume and CSF pTau181. FINDINGS: The threshold for positivity was 15.085 pg/mL for plasma pTau181 and 17.652 pg/mL for plasma pTau231. Most individuals had concordant statuses, however, 18% of plasma181/PET, 26% of plasma231/PET and 25% of the pTau231/pTau181 were discordant. Positivity to at least one biomarker was often accompanied by diagnosis of cognitive impairment, Aβ positivity, APOEε4 carriership, higher levels of [(18)F]AZD4694 global SUVR, hippocampal atrophy and CSF pTau181. INTERPRETATION: Plasma pTau181, pTau231 and [(18)F]MK6240 seem to reflect different stages of tau progression. Plasma biomarkers can be useful in the context of diagnostic information and clinical trials, to evaluate the disease stage. Moreover, they seem to confidently evaluate tau-PET positivity. FUNDING: Moreover, this study was supported by Weston Brain Institute, Canadian Institute of Health Research and Fonds de Recherche du Québec. Elsevier 2022-02-06 /pmc/articles/PMC8844756/ /pubmed/35134647 http://dx.doi.org/10.1016/j.ebiom.2022.103837 Text en © 2022 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Articles
Tissot, Cécile
Therriault, Joseph
Kunach, Peter
L Benedet, Andréa
Pascoal, Tharick A.
Ashton, Nicholas J.
Karikari, Thomas K.
Servaes, Stijn
Lussier, Firoza Z.
Chamoun, Mira
Tudorascu, Dana L.
Stevenson, Jenna
Rahmouni, Nesrine
Poltronetti, Nina Margherita
Pallen, Vanessa
Bezgin, Gleb
Kang, Min Su
Mathotaarachchi, Sulantha S.
Wang, Yi-Ting
Fernandez Arias, Jaime
Ferreira, Pamela Cristina Lukasewicz
Ferrari-Souza, João Pedro
Vanmechelen, Eugeen
Blennow, Kaj
Zetterberg, Henrik
Gauthier, Serge
Rosa-Neto, Pedro
Comparing tau status determined via plasma pTau181, pTau231 and [(18)F]MK6240 tau-PET
title Comparing tau status determined via plasma pTau181, pTau231 and [(18)F]MK6240 tau-PET
title_full Comparing tau status determined via plasma pTau181, pTau231 and [(18)F]MK6240 tau-PET
title_fullStr Comparing tau status determined via plasma pTau181, pTau231 and [(18)F]MK6240 tau-PET
title_full_unstemmed Comparing tau status determined via plasma pTau181, pTau231 and [(18)F]MK6240 tau-PET
title_short Comparing tau status determined via plasma pTau181, pTau231 and [(18)F]MK6240 tau-PET
title_sort comparing tau status determined via plasma ptau181, ptau231 and [(18)f]mk6240 tau-pet
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8844756/
https://www.ncbi.nlm.nih.gov/pubmed/35134647
http://dx.doi.org/10.1016/j.ebiom.2022.103837
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