Combination of white matter hyperintensities and Aβ burden is related to cognitive composites domain scores in subjective cognitive decline: the FACEHBI cohort
Abstract Background To explore whether the combination of white matter hyperintensities (WMHs) and amyloid-beta (Aβ) deposition is associated with worse cognitive performance on cognitive composites (CCs) domain scores in individuals with subjective cognitive decline (SCD). Methods Two hundred parti...
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2021-08-01
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Series: | Alzheimer’s Research & Therapy |
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Online Access: | https://doi.org/10.1186/s13195-021-00877-6 |
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Article |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
G. Ortega A. Espinosa M. Alegret GC. Monté-Rubio O. Sotolongo-Grau A. Sanabria JP. Tartari O. Rodríguez-Gómez M. Marquié A. Vivas M. Gómez-Chiari E. Alarcón-Martín A. Pérez-Cordón N. Roberto I. Hernández M. Rosende-Roca L. Vargas A. Mauleón C. Abdelnour E. Esteban De Antonio R. López-Cuevas S. Alonso-Lana S. Moreno-Grau I. de Rojas A. Orellana L. Montrreal L. Tárraga A. Ruiz M. Boada S. Valero FACEHBI group |
spellingShingle |
G. Ortega A. Espinosa M. Alegret GC. Monté-Rubio O. Sotolongo-Grau A. Sanabria JP. Tartari O. Rodríguez-Gómez M. Marquié A. Vivas M. Gómez-Chiari E. Alarcón-Martín A. Pérez-Cordón N. Roberto I. Hernández M. Rosende-Roca L. Vargas A. Mauleón C. Abdelnour E. Esteban De Antonio R. López-Cuevas S. Alonso-Lana S. Moreno-Grau I. de Rojas A. Orellana L. Montrreal L. Tárraga A. Ruiz M. Boada S. Valero FACEHBI group Combination of white matter hyperintensities and Aβ burden is related to cognitive composites domain scores in subjective cognitive decline: the FACEHBI cohort Alzheimer’s Research & Therapy Amyloid-beta (Aß) Apolipoprotein E Cognitive composites domain scores FBB-PET Magnetic resonance imaging Subjective cognitive decline |
author_facet |
G. Ortega A. Espinosa M. Alegret GC. Monté-Rubio O. Sotolongo-Grau A. Sanabria JP. Tartari O. Rodríguez-Gómez M. Marquié A. Vivas M. Gómez-Chiari E. Alarcón-Martín A. Pérez-Cordón N. Roberto I. Hernández M. Rosende-Roca L. Vargas A. Mauleón C. Abdelnour E. Esteban De Antonio R. López-Cuevas S. Alonso-Lana S. Moreno-Grau I. de Rojas A. Orellana L. Montrreal L. Tárraga A. Ruiz M. Boada S. Valero FACEHBI group |
author_sort |
G. Ortega |
title |
Combination of white matter hyperintensities and Aβ burden is related to cognitive composites domain scores in subjective cognitive decline: the FACEHBI cohort |
title_short |
Combination of white matter hyperintensities and Aβ burden is related to cognitive composites domain scores in subjective cognitive decline: the FACEHBI cohort |
title_full |
Combination of white matter hyperintensities and Aβ burden is related to cognitive composites domain scores in subjective cognitive decline: the FACEHBI cohort |
title_fullStr |
Combination of white matter hyperintensities and Aβ burden is related to cognitive composites domain scores in subjective cognitive decline: the FACEHBI cohort |
title_full_unstemmed |
Combination of white matter hyperintensities and Aβ burden is related to cognitive composites domain scores in subjective cognitive decline: the FACEHBI cohort |
title_sort |
combination of white matter hyperintensities and aβ burden is related to cognitive composites domain scores in subjective cognitive decline: the facehbi cohort |
publisher |
BMC |
series |
Alzheimer’s Research & Therapy |
issn |
1758-9193 |
publishDate |
2021-08-01 |
description |
Abstract Background To explore whether the combination of white matter hyperintensities (WMHs) and amyloid-beta (Aβ) deposition is associated with worse cognitive performance on cognitive composites (CCs) domain scores in individuals with subjective cognitive decline (SCD). Methods Two hundred participants from the FACEHBI cohort underwent structural magnetic resonance imaging (MRI), 18F-florbetaben positron emission tomography (FBB-PET), and neuropsychological assessment. WMHs were addressed through the Fazekas scale, the Age-Related White Matter Changes (ARWMC) scale, and the FreeSurfer pipeline. Eight CCs domain scores were created using the principal component analysis (PCA). Age, sex, education, and apolipoprotein E (APOE) were used as adjusting variables. Results Adjusted multiple linear regression models showed that FreeSurfer (B − .245; 95% CI − .1.676, − .393, p = .016) and β burden (SUVR) (B − .180; 95% CI − 2.140, − .292; p = .070) were associated with face–name associative memory CCs domain score, although the latest one was not statistically significant after correction for multiple testing (p = .070). There was non-significant interaction of these two factors on this same CCs domain score (p = .54). However, its cumulative effects on face–name associative performance indicated that those individuals with either higher WMH load or higher Aβ burden showed the worst performance on the face–name associative memory CCs domain score. Conclusions Our results suggest that increased WMH load and increased Aβ are independently associated with poorer episodic memory performance in SCD individuals, indicating a cumulative effect of the combination of these two pathological conditions in promoting lower cognitive performance, an aspect that could help in terms of treatment and prevention. |
topic |
Amyloid-beta (Aß) Apolipoprotein E Cognitive composites domain scores FBB-PET Magnetic resonance imaging Subjective cognitive decline |
url |
https://doi.org/10.1186/s13195-021-00877-6 |
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doaj-c2fb77c0ab0740a1a9845aa81bf901e72021-08-22T11:44:04ZengBMCAlzheimer’s Research & Therapy1758-91932021-08-0113111110.1186/s13195-021-00877-6Combination of white matter hyperintensities and Aβ burden is related to cognitive composites domain scores in subjective cognitive decline: the FACEHBI cohortG. Ortega0A. Espinosa1M. Alegret2GC. Monté-Rubio3O. Sotolongo-Grau4A. Sanabria5JP. Tartari6O. Rodríguez-Gómez7M. Marquié8A. Vivas9M. Gómez-Chiari10E. Alarcón-Martín11A. Pérez-Cordón12N. Roberto13I. Hernández14M. Rosende-Roca15L. Vargas16A. Mauleón17C. Abdelnour18E. Esteban De Antonio19R. López-Cuevas20S. Alonso-Lana21S. Moreno-Grau22I. de Rojas23A. Orellana24L. Montrreal25L. Tárraga26A. Ruiz27M. Boada28S. Valero29FACEHBI groupFundació ACE, Institut Català de Neurociències Aplicades, Research Center and Memory Clinic, Universitat Internacional de Catalunya, C/ Gran Via de Carles IIIFundació ACE, Institut Català de Neurociències Aplicades, Research Center and Memory Clinic, Universitat Internacional de Catalunya, C/ Gran Via de Carles IIIFundació ACE, Institut Català de Neurociències Aplicades, Research Center and Memory Clinic, Universitat Internacional de Catalunya, C/ Gran Via de Carles IIIFundació ACE, Institut Català de Neurociències Aplicades, Research Center and Memory Clinic, Universitat Internacional de Catalunya, C/ Gran Via de Carles IIIFundació ACE, Institut Català de Neurociències Aplicades, Research Center and Memory Clinic, Universitat Internacional de Catalunya, C/ Gran Via de Carles IIIFundació ACE, Institut Català de Neurociències Aplicades, Research Center and Memory Clinic, Universitat Internacional de Catalunya, C/ Gran Via de Carles IIIFundació ACE, Institut Català de Neurociències Aplicades, Research Center and Memory Clinic, Universitat Internacional de Catalunya, C/ Gran Via de Carles IIIFundació ACE, Institut Català de Neurociències Aplicades, Research Center and Memory Clinic, Universitat Internacional de Catalunya, C/ Gran Via de Carles IIIFundació ACE, Institut Català de Neurociències Aplicades, Research Center and Memory Clinic, Universitat Internacional de Catalunya, C/ Gran Via de Carles IIIDepartament de Diagnòstic Per La Imatge, Clínica CorachanDepartament de Diagnòstic Per La Imatge, Clínica CorachanFundació ACE, Institut Català de Neurociències Aplicades, Research Center and Memory Clinic, Universitat Internacional de Catalunya, C/ Gran Via de Carles IIIFundació ACE, Institut Català de Neurociències Aplicades, Research Center and Memory Clinic, Universitat Internacional de Catalunya, C/ Gran Via de Carles IIIFundació ACE, Institut Català de Neurociències Aplicades, Research Center and Memory Clinic, Universitat Internacional de Catalunya, C/ Gran Via de Carles IIIFundació ACE, Institut Català de Neurociències Aplicades, Research Center and Memory Clinic, Universitat Internacional de Catalunya, C/ Gran Via de Carles IIIFundació ACE, Institut Català de Neurociències Aplicades, Research Center and Memory Clinic, Universitat Internacional de Catalunya, C/ Gran Via de Carles IIIFundació ACE, Institut Català de Neurociències Aplicades, Research Center and Memory Clinic, Universitat Internacional de Catalunya, C/ Gran Via de Carles IIIFundació ACE, Institut Català de Neurociències Aplicades, Research Center and Memory Clinic, Universitat Internacional de Catalunya, C/ Gran Via de Carles IIIFundació ACE, Institut Català de Neurociències Aplicades, Research Center and Memory Clinic, Universitat Internacional de Catalunya, C/ Gran Via de Carles IIIFundació ACE, Institut Català de Neurociències Aplicades, Research Center and Memory Clinic, Universitat Internacional de Catalunya, C/ Gran Via de Carles IIIFundació ACE, Institut Català de Neurociències Aplicades, Research Center and Memory Clinic, Universitat Internacional de Catalunya, C/ Gran Via de Carles IIIFundació ACE, Institut Català de Neurociències Aplicades, Research Center and Memory Clinic, Universitat Internacional de Catalunya, C/ Gran Via de Carles IIIFundació ACE, Institut Català de Neurociències Aplicades, Research Center and Memory Clinic, Universitat Internacional de Catalunya, C/ Gran Via de Carles IIIFundació ACE, Institut Català de Neurociències Aplicades, Research Center and Memory Clinic, Universitat Internacional de Catalunya, C/ Gran Via de Carles IIIFundació ACE, Institut Català de Neurociències Aplicades, Research Center and Memory Clinic, Universitat Internacional de Catalunya, C/ Gran Via de Carles IIIFundació ACE, Institut Català de Neurociències Aplicades, Research Center and Memory Clinic, Universitat Internacional de Catalunya, C/ Gran Via de Carles IIIFundació ACE, Institut Català de Neurociències Aplicades, Research Center and Memory Clinic, Universitat Internacional de Catalunya, C/ Gran Via de Carles IIIFundació ACE, Institut Català de Neurociències Aplicades, Research Center and Memory Clinic, Universitat Internacional de Catalunya, C/ Gran Via de Carles IIIFundació ACE, Institut Català de Neurociències Aplicades, Research Center and Memory Clinic, Universitat Internacional de Catalunya, C/ Gran Via de Carles IIIFundació ACE, Institut Català de Neurociències Aplicades, Research Center and Memory Clinic, Universitat Internacional de Catalunya, C/ Gran Via de Carles IIIAbstract Background To explore whether the combination of white matter hyperintensities (WMHs) and amyloid-beta (Aβ) deposition is associated with worse cognitive performance on cognitive composites (CCs) domain scores in individuals with subjective cognitive decline (SCD). Methods Two hundred participants from the FACEHBI cohort underwent structural magnetic resonance imaging (MRI), 18F-florbetaben positron emission tomography (FBB-PET), and neuropsychological assessment. WMHs were addressed through the Fazekas scale, the Age-Related White Matter Changes (ARWMC) scale, and the FreeSurfer pipeline. Eight CCs domain scores were created using the principal component analysis (PCA). Age, sex, education, and apolipoprotein E (APOE) were used as adjusting variables. Results Adjusted multiple linear regression models showed that FreeSurfer (B − .245; 95% CI − .1.676, − .393, p = .016) and β burden (SUVR) (B − .180; 95% CI − 2.140, − .292; p = .070) were associated with face–name associative memory CCs domain score, although the latest one was not statistically significant after correction for multiple testing (p = .070). There was non-significant interaction of these two factors on this same CCs domain score (p = .54). However, its cumulative effects on face–name associative performance indicated that those individuals with either higher WMH load or higher Aβ burden showed the worst performance on the face–name associative memory CCs domain score. Conclusions Our results suggest that increased WMH load and increased Aβ are independently associated with poorer episodic memory performance in SCD individuals, indicating a cumulative effect of the combination of these two pathological conditions in promoting lower cognitive performance, an aspect that could help in terms of treatment and prevention.https://doi.org/10.1186/s13195-021-00877-6Amyloid-beta (Aß)Apolipoprotein ECognitive composites domain scoresFBB-PETMagnetic resonance imagingSubjective cognitive decline |