Cargando…

The Cerebrospinal Fluid Aβ(1–42)/Aβ(1–40) Ratio Improves Concordance with Amyloid-PET for Diagnosing Alzheimer’s Disease in a Clinical Setting

BACKGROUND: Evidence suggests that the concordance between amyloid-PET and cerebrospinal fluid (CSF) amyloid-β (Aβ) increases when the CSF Aβ(1–42)/Aβ(1–40) ratio is used as compared to CSF Aβ(1–42) levels alone. OBJECTIVE: In order to test this hypothesis, we set up a prospective longitudinal study...

Descripción completa

Detalles Bibliográficos
Autores principales: Niemantsverdriet, Ellis, Ottoy, Julie, Somers, Charisse, De Roeck, Ellen, Struyfs, Hanne, Soetewey, Femke, Verhaeghe, Jeroen, Van den Bossche, Tobi, Van Mossevelde, Sara, Goeman, Johan, De Deyn, Peter Paul, Mariën, Peter, Versijpt, Jan, Sleegers, Kristel, Van Broeckhoven, Christine, Wyffels, Leonie, Albert, Adrien, Ceyssens, Sarah, Stroobants, Sigrid, Staelens, Steven, Bjerke, Maria, Engelborghs, Sebastiaan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: IOS Press 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5611891/
https://www.ncbi.nlm.nih.gov/pubmed/28869470
http://dx.doi.org/10.3233/JAD-170327
_version_ 1783266031404318720
author Niemantsverdriet, Ellis
Ottoy, Julie
Somers, Charisse
De Roeck, Ellen
Struyfs, Hanne
Soetewey, Femke
Verhaeghe, Jeroen
Van den Bossche, Tobi
Van Mossevelde, Sara
Goeman, Johan
De Deyn, Peter Paul
Mariën, Peter
Versijpt, Jan
Sleegers, Kristel
Van Broeckhoven, Christine
Wyffels, Leonie
Albert, Adrien
Ceyssens, Sarah
Stroobants, Sigrid
Staelens, Steven
Bjerke, Maria
Engelborghs, Sebastiaan
author_facet Niemantsverdriet, Ellis
Ottoy, Julie
Somers, Charisse
De Roeck, Ellen
Struyfs, Hanne
Soetewey, Femke
Verhaeghe, Jeroen
Van den Bossche, Tobi
Van Mossevelde, Sara
Goeman, Johan
De Deyn, Peter Paul
Mariën, Peter
Versijpt, Jan
Sleegers, Kristel
Van Broeckhoven, Christine
Wyffels, Leonie
Albert, Adrien
Ceyssens, Sarah
Stroobants, Sigrid
Staelens, Steven
Bjerke, Maria
Engelborghs, Sebastiaan
author_sort Niemantsverdriet, Ellis
collection PubMed
description BACKGROUND: Evidence suggests that the concordance between amyloid-PET and cerebrospinal fluid (CSF) amyloid-β (Aβ) increases when the CSF Aβ(1–42)/Aβ(1–40) ratio is used as compared to CSF Aβ(1–42) levels alone. OBJECTIVE: In order to test this hypothesis, we set up a prospective longitudinal study comparing the concordance between different amyloid biomarkers for Alzheimer’s disease (AD) in a clinical setting. METHODS: Seventy-eight subjects (AD dementia (n = 17), mild cognitive impairment (MCI, n = 48), and cognitively healthy controls (n = 13)) underwent a [(18)F]Florbetapir ([(18)F]AV45) PET scan, [(18)F]FDG PET scan, MRI scan, and an extensive neuropsychological examination. In a large subset (n = 67), a lumbar puncture was performed and AD biomarkers were analyzed (Aβ(1–42), Aβ(1–40), T-tau, P-tau(181)). RESULTS: We detected an increased concordance in the visual and quantitative (standardized uptake value ratio (SUVR) and total volume of distribution (V(T))) [(18)F]AV45 PET measures when the CSF Aβ(1–42)/Aβ(1–40) was applied compared to Aβ(1–42) alone. CSF biomarkers were stronger associated to [(18)F]AV45 PET for SUVR values when considering the total brain white matter as reference region instead of cerebellar grey matter CONCLUSIONS: The concordance between CSF Aβ and [(18)F]AV45 PET increases when the CSF Aβ(1–42)/Aβ(1–40) ratio is applied. This finding is of most importance for the biomarker-based diagnosis of AD as well as for selection of subjects for clinical trials with potential disease-modifying therapies for AD.
format Online
Article
Text
id pubmed-5611891
institution National Center for Biotechnology Information
language English
publishDate 2017
publisher IOS Press
record_format MEDLINE/PubMed
spelling pubmed-56118912017-10-02 The Cerebrospinal Fluid Aβ(1–42)/Aβ(1–40) Ratio Improves Concordance with Amyloid-PET for Diagnosing Alzheimer’s Disease in a Clinical Setting Niemantsverdriet, Ellis Ottoy, Julie Somers, Charisse De Roeck, Ellen Struyfs, Hanne Soetewey, Femke Verhaeghe, Jeroen Van den Bossche, Tobi Van Mossevelde, Sara Goeman, Johan De Deyn, Peter Paul Mariën, Peter Versijpt, Jan Sleegers, Kristel Van Broeckhoven, Christine Wyffels, Leonie Albert, Adrien Ceyssens, Sarah Stroobants, Sigrid Staelens, Steven Bjerke, Maria Engelborghs, Sebastiaan J Alzheimers Dis Research Article BACKGROUND: Evidence suggests that the concordance between amyloid-PET and cerebrospinal fluid (CSF) amyloid-β (Aβ) increases when the CSF Aβ(1–42)/Aβ(1–40) ratio is used as compared to CSF Aβ(1–42) levels alone. OBJECTIVE: In order to test this hypothesis, we set up a prospective longitudinal study comparing the concordance between different amyloid biomarkers for Alzheimer’s disease (AD) in a clinical setting. METHODS: Seventy-eight subjects (AD dementia (n = 17), mild cognitive impairment (MCI, n = 48), and cognitively healthy controls (n = 13)) underwent a [(18)F]Florbetapir ([(18)F]AV45) PET scan, [(18)F]FDG PET scan, MRI scan, and an extensive neuropsychological examination. In a large subset (n = 67), a lumbar puncture was performed and AD biomarkers were analyzed (Aβ(1–42), Aβ(1–40), T-tau, P-tau(181)). RESULTS: We detected an increased concordance in the visual and quantitative (standardized uptake value ratio (SUVR) and total volume of distribution (V(T))) [(18)F]AV45 PET measures when the CSF Aβ(1–42)/Aβ(1–40) was applied compared to Aβ(1–42) alone. CSF biomarkers were stronger associated to [(18)F]AV45 PET for SUVR values when considering the total brain white matter as reference region instead of cerebellar grey matter CONCLUSIONS: The concordance between CSF Aβ and [(18)F]AV45 PET increases when the CSF Aβ(1–42)/Aβ(1–40) ratio is applied. This finding is of most importance for the biomarker-based diagnosis of AD as well as for selection of subjects for clinical trials with potential disease-modifying therapies for AD. IOS Press 2017-09-18 /pmc/articles/PMC5611891/ /pubmed/28869470 http://dx.doi.org/10.3233/JAD-170327 Text en © 2017 – IOS Press and the authors. All rights reserved https://creativecommons.org/licenses/by-nc/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution Non-Commercial (CC BY-NC 4.0) License (https://creativecommons.org/licenses/by-nc/4.0/) , which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Niemantsverdriet, Ellis
Ottoy, Julie
Somers, Charisse
De Roeck, Ellen
Struyfs, Hanne
Soetewey, Femke
Verhaeghe, Jeroen
Van den Bossche, Tobi
Van Mossevelde, Sara
Goeman, Johan
De Deyn, Peter Paul
Mariën, Peter
Versijpt, Jan
Sleegers, Kristel
Van Broeckhoven, Christine
Wyffels, Leonie
Albert, Adrien
Ceyssens, Sarah
Stroobants, Sigrid
Staelens, Steven
Bjerke, Maria
Engelborghs, Sebastiaan
The Cerebrospinal Fluid Aβ(1–42)/Aβ(1–40) Ratio Improves Concordance with Amyloid-PET for Diagnosing Alzheimer’s Disease in a Clinical Setting
title The Cerebrospinal Fluid Aβ(1–42)/Aβ(1–40) Ratio Improves Concordance with Amyloid-PET for Diagnosing Alzheimer’s Disease in a Clinical Setting
title_full The Cerebrospinal Fluid Aβ(1–42)/Aβ(1–40) Ratio Improves Concordance with Amyloid-PET for Diagnosing Alzheimer’s Disease in a Clinical Setting
title_fullStr The Cerebrospinal Fluid Aβ(1–42)/Aβ(1–40) Ratio Improves Concordance with Amyloid-PET for Diagnosing Alzheimer’s Disease in a Clinical Setting
title_full_unstemmed The Cerebrospinal Fluid Aβ(1–42)/Aβ(1–40) Ratio Improves Concordance with Amyloid-PET for Diagnosing Alzheimer’s Disease in a Clinical Setting
title_short The Cerebrospinal Fluid Aβ(1–42)/Aβ(1–40) Ratio Improves Concordance with Amyloid-PET for Diagnosing Alzheimer’s Disease in a Clinical Setting
title_sort cerebrospinal fluid aβ(1–42)/aβ(1–40) ratio improves concordance with amyloid-pet for diagnosing alzheimer’s disease in a clinical setting
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5611891/
https://www.ncbi.nlm.nih.gov/pubmed/28869470
http://dx.doi.org/10.3233/JAD-170327
work_keys_str_mv AT niemantsverdrietellis thecerebrospinalfluidab142ab140ratioimprovesconcordancewithamyloidpetfordiagnosingalzheimersdiseaseinaclinicalsetting
AT ottoyjulie thecerebrospinalfluidab142ab140ratioimprovesconcordancewithamyloidpetfordiagnosingalzheimersdiseaseinaclinicalsetting
AT somerscharisse thecerebrospinalfluidab142ab140ratioimprovesconcordancewithamyloidpetfordiagnosingalzheimersdiseaseinaclinicalsetting
AT deroeckellen thecerebrospinalfluidab142ab140ratioimprovesconcordancewithamyloidpetfordiagnosingalzheimersdiseaseinaclinicalsetting
AT struyfshanne thecerebrospinalfluidab142ab140ratioimprovesconcordancewithamyloidpetfordiagnosingalzheimersdiseaseinaclinicalsetting
AT soeteweyfemke thecerebrospinalfluidab142ab140ratioimprovesconcordancewithamyloidpetfordiagnosingalzheimersdiseaseinaclinicalsetting
AT verhaeghejeroen thecerebrospinalfluidab142ab140ratioimprovesconcordancewithamyloidpetfordiagnosingalzheimersdiseaseinaclinicalsetting
AT vandenbosschetobi thecerebrospinalfluidab142ab140ratioimprovesconcordancewithamyloidpetfordiagnosingalzheimersdiseaseinaclinicalsetting
AT vanmosseveldesara thecerebrospinalfluidab142ab140ratioimprovesconcordancewithamyloidpetfordiagnosingalzheimersdiseaseinaclinicalsetting
AT goemanjohan thecerebrospinalfluidab142ab140ratioimprovesconcordancewithamyloidpetfordiagnosingalzheimersdiseaseinaclinicalsetting
AT dedeynpeterpaul thecerebrospinalfluidab142ab140ratioimprovesconcordancewithamyloidpetfordiagnosingalzheimersdiseaseinaclinicalsetting
AT marienpeter thecerebrospinalfluidab142ab140ratioimprovesconcordancewithamyloidpetfordiagnosingalzheimersdiseaseinaclinicalsetting
AT versijptjan thecerebrospinalfluidab142ab140ratioimprovesconcordancewithamyloidpetfordiagnosingalzheimersdiseaseinaclinicalsetting
AT sleegerskristel thecerebrospinalfluidab142ab140ratioimprovesconcordancewithamyloidpetfordiagnosingalzheimersdiseaseinaclinicalsetting
AT vanbroeckhovenchristine thecerebrospinalfluidab142ab140ratioimprovesconcordancewithamyloidpetfordiagnosingalzheimersdiseaseinaclinicalsetting
AT wyffelsleonie thecerebrospinalfluidab142ab140ratioimprovesconcordancewithamyloidpetfordiagnosingalzheimersdiseaseinaclinicalsetting
AT albertadrien thecerebrospinalfluidab142ab140ratioimprovesconcordancewithamyloidpetfordiagnosingalzheimersdiseaseinaclinicalsetting
AT ceyssenssarah thecerebrospinalfluidab142ab140ratioimprovesconcordancewithamyloidpetfordiagnosingalzheimersdiseaseinaclinicalsetting
AT stroobantssigrid thecerebrospinalfluidab142ab140ratioimprovesconcordancewithamyloidpetfordiagnosingalzheimersdiseaseinaclinicalsetting
AT staelenssteven thecerebrospinalfluidab142ab140ratioimprovesconcordancewithamyloidpetfordiagnosingalzheimersdiseaseinaclinicalsetting
AT bjerkemaria thecerebrospinalfluidab142ab140ratioimprovesconcordancewithamyloidpetfordiagnosingalzheimersdiseaseinaclinicalsetting
AT engelborghssebastiaan thecerebrospinalfluidab142ab140ratioimprovesconcordancewithamyloidpetfordiagnosingalzheimersdiseaseinaclinicalsetting
AT niemantsverdrietellis cerebrospinalfluidab142ab140ratioimprovesconcordancewithamyloidpetfordiagnosingalzheimersdiseaseinaclinicalsetting
AT ottoyjulie cerebrospinalfluidab142ab140ratioimprovesconcordancewithamyloidpetfordiagnosingalzheimersdiseaseinaclinicalsetting
AT somerscharisse cerebrospinalfluidab142ab140ratioimprovesconcordancewithamyloidpetfordiagnosingalzheimersdiseaseinaclinicalsetting
AT deroeckellen cerebrospinalfluidab142ab140ratioimprovesconcordancewithamyloidpetfordiagnosingalzheimersdiseaseinaclinicalsetting
AT struyfshanne cerebrospinalfluidab142ab140ratioimprovesconcordancewithamyloidpetfordiagnosingalzheimersdiseaseinaclinicalsetting
AT soeteweyfemke cerebrospinalfluidab142ab140ratioimprovesconcordancewithamyloidpetfordiagnosingalzheimersdiseaseinaclinicalsetting
AT verhaeghejeroen cerebrospinalfluidab142ab140ratioimprovesconcordancewithamyloidpetfordiagnosingalzheimersdiseaseinaclinicalsetting
AT vandenbosschetobi cerebrospinalfluidab142ab140ratioimprovesconcordancewithamyloidpetfordiagnosingalzheimersdiseaseinaclinicalsetting
AT vanmosseveldesara cerebrospinalfluidab142ab140ratioimprovesconcordancewithamyloidpetfordiagnosingalzheimersdiseaseinaclinicalsetting
AT goemanjohan cerebrospinalfluidab142ab140ratioimprovesconcordancewithamyloidpetfordiagnosingalzheimersdiseaseinaclinicalsetting
AT dedeynpeterpaul cerebrospinalfluidab142ab140ratioimprovesconcordancewithamyloidpetfordiagnosingalzheimersdiseaseinaclinicalsetting
AT marienpeter cerebrospinalfluidab142ab140ratioimprovesconcordancewithamyloidpetfordiagnosingalzheimersdiseaseinaclinicalsetting
AT versijptjan cerebrospinalfluidab142ab140ratioimprovesconcordancewithamyloidpetfordiagnosingalzheimersdiseaseinaclinicalsetting
AT sleegerskristel cerebrospinalfluidab142ab140ratioimprovesconcordancewithamyloidpetfordiagnosingalzheimersdiseaseinaclinicalsetting
AT vanbroeckhovenchristine cerebrospinalfluidab142ab140ratioimprovesconcordancewithamyloidpetfordiagnosingalzheimersdiseaseinaclinicalsetting
AT wyffelsleonie cerebrospinalfluidab142ab140ratioimprovesconcordancewithamyloidpetfordiagnosingalzheimersdiseaseinaclinicalsetting
AT albertadrien cerebrospinalfluidab142ab140ratioimprovesconcordancewithamyloidpetfordiagnosingalzheimersdiseaseinaclinicalsetting
AT ceyssenssarah cerebrospinalfluidab142ab140ratioimprovesconcordancewithamyloidpetfordiagnosingalzheimersdiseaseinaclinicalsetting
AT stroobantssigrid cerebrospinalfluidab142ab140ratioimprovesconcordancewithamyloidpetfordiagnosingalzheimersdiseaseinaclinicalsetting
AT staelenssteven cerebrospinalfluidab142ab140ratioimprovesconcordancewithamyloidpetfordiagnosingalzheimersdiseaseinaclinicalsetting
AT bjerkemaria cerebrospinalfluidab142ab140ratioimprovesconcordancewithamyloidpetfordiagnosingalzheimersdiseaseinaclinicalsetting
AT engelborghssebastiaan cerebrospinalfluidab142ab140ratioimprovesconcordancewithamyloidpetfordiagnosingalzheimersdiseaseinaclinicalsetting