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Pittsburgh compound B imaging and cerebrospinal fluid amyloid-β in a multicentre European memory clinic study

The aim of this study was to assess the agreement between data on cerebral amyloidosis, derived using Pittsburgh compound B positron emission tomography and (i) multi-laboratory INNOTEST enzyme linked immunosorbent assay derived cerebrospinal fluid concentrations of amyloid-β(42); (ii) centrally mea...

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Autores principales: Leuzy, Antoine, Chiotis, Konstantinos, Hasselbalch, Steen G., Rinne, Juha O., de Mendonça, Alexandre, Otto, Markus, Lleó, Alberto, Castelo-Branco, Miguel, Santana, Isabel, Johansson, Jarkko, Anderl-Straub, Sarah, von Arnim, Christine A. F., Beer, Ambros, Blesa, Rafael, Fortea, Juan, Herukka, Sanna-Kaisa, Portelius, Erik, Pannee, Josef, Zetterberg, Henrik, Blennow, Kaj, Nordberg, Agneta
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4995359/
https://www.ncbi.nlm.nih.gov/pubmed/27401520
http://dx.doi.org/10.1093/brain/aww160
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author Leuzy, Antoine
Chiotis, Konstantinos
Hasselbalch, Steen G.
Rinne, Juha O.
de Mendonça, Alexandre
Otto, Markus
Lleó, Alberto
Castelo-Branco, Miguel
Santana, Isabel
Johansson, Jarkko
Anderl-Straub, Sarah
von Arnim, Christine A. F.
Beer, Ambros
Blesa, Rafael
Fortea, Juan
Herukka, Sanna-Kaisa
Portelius, Erik
Pannee, Josef
Zetterberg, Henrik
Blennow, Kaj
Nordberg, Agneta
author_facet Leuzy, Antoine
Chiotis, Konstantinos
Hasselbalch, Steen G.
Rinne, Juha O.
de Mendonça, Alexandre
Otto, Markus
Lleó, Alberto
Castelo-Branco, Miguel
Santana, Isabel
Johansson, Jarkko
Anderl-Straub, Sarah
von Arnim, Christine A. F.
Beer, Ambros
Blesa, Rafael
Fortea, Juan
Herukka, Sanna-Kaisa
Portelius, Erik
Pannee, Josef
Zetterberg, Henrik
Blennow, Kaj
Nordberg, Agneta
author_sort Leuzy, Antoine
collection PubMed
description The aim of this study was to assess the agreement between data on cerebral amyloidosis, derived using Pittsburgh compound B positron emission tomography and (i) multi-laboratory INNOTEST enzyme linked immunosorbent assay derived cerebrospinal fluid concentrations of amyloid-β(42); (ii) centrally measured cerebrospinal fluid amyloid-β(42) using a Meso Scale Discovery enzyme linked immunosorbent assay; and (iii) cerebrospinal fluid amyloid-β(42) centrally measured using an antibody-independent mass spectrometry-based reference method. Moreover, we examined the hypothesis that discordance between amyloid biomarker measurements may be due to interindividual differences in total amyloid-β production, by using the ratio of amyloid-β(42) to amyloid-β(40). Our study population consisted of 243 subjects from seven centres belonging to the Biomarkers for Alzheimer’s and Parkinson’s Disease Initiative, and included subjects with normal cognition and patients with mild cognitive impairment, Alzheimer’s disease dementia, frontotemporal dementia, and vascular dementia. All had Pittsburgh compound B positron emission tomography data, cerebrospinal fluid INNOTEST amyloid-β(42) values, and cerebrospinal fluid samples available for reanalysis. Cerebrospinal fluid samples were reanalysed (amyloid-β(42) and amyloid-β(40)) using Meso Scale Discovery electrochemiluminescence enzyme linked immunosorbent assay technology, and a novel, antibody-independent, mass spectrometry reference method. Pittsburgh compound B standardized uptake value ratio results were scaled using the Centiloid method. Concordance between Meso Scale Discovery/mass spectrometry reference measurement procedure findings and Pittsburgh compound B was high in subjects with mild cognitive impairment and Alzheimer’s disease, while more variable results were observed for cognitively normal and non-Alzheimer’s disease groups. Agreement between Pittsburgh compound B classification and Meso Scale Discovery/mass spectrometry reference measurement procedure findings was further improved when using amyloid-β(42/40). Agreement between Pittsburgh compound B visual ratings and Centiloids was near complete. Despite improved agreement between Pittsburgh compound B and centrally analysed cerebrospinal fluid, a minority of subjects showed discordant findings. While future studies are needed, our results suggest that amyloid biomarker results may not be interchangeable in some individuals.
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spelling pubmed-49953592016-08-25 Pittsburgh compound B imaging and cerebrospinal fluid amyloid-β in a multicentre European memory clinic study Leuzy, Antoine Chiotis, Konstantinos Hasselbalch, Steen G. Rinne, Juha O. de Mendonça, Alexandre Otto, Markus Lleó, Alberto Castelo-Branco, Miguel Santana, Isabel Johansson, Jarkko Anderl-Straub, Sarah von Arnim, Christine A. F. Beer, Ambros Blesa, Rafael Fortea, Juan Herukka, Sanna-Kaisa Portelius, Erik Pannee, Josef Zetterberg, Henrik Blennow, Kaj Nordberg, Agneta Brain Original Articles The aim of this study was to assess the agreement between data on cerebral amyloidosis, derived using Pittsburgh compound B positron emission tomography and (i) multi-laboratory INNOTEST enzyme linked immunosorbent assay derived cerebrospinal fluid concentrations of amyloid-β(42); (ii) centrally measured cerebrospinal fluid amyloid-β(42) using a Meso Scale Discovery enzyme linked immunosorbent assay; and (iii) cerebrospinal fluid amyloid-β(42) centrally measured using an antibody-independent mass spectrometry-based reference method. Moreover, we examined the hypothesis that discordance between amyloid biomarker measurements may be due to interindividual differences in total amyloid-β production, by using the ratio of amyloid-β(42) to amyloid-β(40). Our study population consisted of 243 subjects from seven centres belonging to the Biomarkers for Alzheimer’s and Parkinson’s Disease Initiative, and included subjects with normal cognition and patients with mild cognitive impairment, Alzheimer’s disease dementia, frontotemporal dementia, and vascular dementia. All had Pittsburgh compound B positron emission tomography data, cerebrospinal fluid INNOTEST amyloid-β(42) values, and cerebrospinal fluid samples available for reanalysis. Cerebrospinal fluid samples were reanalysed (amyloid-β(42) and amyloid-β(40)) using Meso Scale Discovery electrochemiluminescence enzyme linked immunosorbent assay technology, and a novel, antibody-independent, mass spectrometry reference method. Pittsburgh compound B standardized uptake value ratio results were scaled using the Centiloid method. Concordance between Meso Scale Discovery/mass spectrometry reference measurement procedure findings and Pittsburgh compound B was high in subjects with mild cognitive impairment and Alzheimer’s disease, while more variable results were observed for cognitively normal and non-Alzheimer’s disease groups. Agreement between Pittsburgh compound B classification and Meso Scale Discovery/mass spectrometry reference measurement procedure findings was further improved when using amyloid-β(42/40). Agreement between Pittsburgh compound B visual ratings and Centiloids was near complete. Despite improved agreement between Pittsburgh compound B and centrally analysed cerebrospinal fluid, a minority of subjects showed discordant findings. While future studies are needed, our results suggest that amyloid biomarker results may not be interchangeable in some individuals. Oxford University Press 2016-09 2016-07-07 /pmc/articles/PMC4995359/ /pubmed/27401520 http://dx.doi.org/10.1093/brain/aww160 Text en © The Author (2016). Published by Oxford University Press on behalf of the Guarantors of Brain. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Original Articles
Leuzy, Antoine
Chiotis, Konstantinos
Hasselbalch, Steen G.
Rinne, Juha O.
de Mendonça, Alexandre
Otto, Markus
Lleó, Alberto
Castelo-Branco, Miguel
Santana, Isabel
Johansson, Jarkko
Anderl-Straub, Sarah
von Arnim, Christine A. F.
Beer, Ambros
Blesa, Rafael
Fortea, Juan
Herukka, Sanna-Kaisa
Portelius, Erik
Pannee, Josef
Zetterberg, Henrik
Blennow, Kaj
Nordberg, Agneta
Pittsburgh compound B imaging and cerebrospinal fluid amyloid-β in a multicentre European memory clinic study
title Pittsburgh compound B imaging and cerebrospinal fluid amyloid-β in a multicentre European memory clinic study
title_full Pittsburgh compound B imaging and cerebrospinal fluid amyloid-β in a multicentre European memory clinic study
title_fullStr Pittsburgh compound B imaging and cerebrospinal fluid amyloid-β in a multicentre European memory clinic study
title_full_unstemmed Pittsburgh compound B imaging and cerebrospinal fluid amyloid-β in a multicentre European memory clinic study
title_short Pittsburgh compound B imaging and cerebrospinal fluid amyloid-β in a multicentre European memory clinic study
title_sort pittsburgh compound b imaging and cerebrospinal fluid amyloid-β in a multicentre european memory clinic study
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4995359/
https://www.ncbi.nlm.nih.gov/pubmed/27401520
http://dx.doi.org/10.1093/brain/aww160
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