Cargando…

Data-driven FDG-PET subtypes of Alzheimer’s disease-related neurodegeneration

BACKGROUND: Previous research has described distinct subtypes of Alzheimer’s disease (AD) based on the differences in regional patterns of brain atrophy on MRI. We conducted a data-driven exploration of distinct AD neurodegeneration subtypes using FDG-PET as a sensitive molecular imaging marker of n...

Descripción completa

Detalles Bibliográficos
Autores principales: Levin, Fedor, Ferreira, Daniel, Lange, Catharina, Dyrba, Martin, Westman, Eric, Buchert, Ralph, Teipel, Stefan J., Grothe, Michel J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7896407/
https://www.ncbi.nlm.nih.gov/pubmed/33608059
http://dx.doi.org/10.1186/s13195-021-00785-9
_version_ 1783653536892977152
author Levin, Fedor
Ferreira, Daniel
Lange, Catharina
Dyrba, Martin
Westman, Eric
Buchert, Ralph
Teipel, Stefan J.
Grothe, Michel J.
author_facet Levin, Fedor
Ferreira, Daniel
Lange, Catharina
Dyrba, Martin
Westman, Eric
Buchert, Ralph
Teipel, Stefan J.
Grothe, Michel J.
author_sort Levin, Fedor
collection PubMed
description BACKGROUND: Previous research has described distinct subtypes of Alzheimer’s disease (AD) based on the differences in regional patterns of brain atrophy on MRI. We conducted a data-driven exploration of distinct AD neurodegeneration subtypes using FDG-PET as a sensitive molecular imaging marker of neurodegenerative processes. METHODS: Hierarchical clustering of voxel-wise FDG-PET data from 177 amyloid-positive patients with AD dementia enrolled in the Alzheimer’s Disease Neuroimaging Initiative (ADNI) was used to identify distinct hypometabolic subtypes of AD, which were then further characterized with respect to clinical and biomarker characteristics. We then classified FDG-PET scans of 217 amyloid-positive patients with mild cognitive impairment (“prodromal AD”) according to the identified subtypes and studied their domain-specific cognitive trajectories and progression to dementia over a follow-up interval of up to 72 months. RESULTS: Three main hypometabolic subtypes were identified: (i) “typical” (48.6%), showing a classic posterior temporo-parietal hypometabolic pattern; (ii) “limbic-predominant” (44.6%), characterized by old age and a memory-predominant cognitive profile; and (iii) a relatively rare “cortical-predominant” subtype (6.8%) characterized by younger age and more severe executive dysfunction. Subtypes classified in the prodromal AD sample demonstrated similar subtype characteristics as in the AD dementia sample and further showed differential courses of cognitive decline. CONCLUSIONS: These findings complement recent research efforts on MRI-based identification of distinct AD atrophy subtypes and may provide a potentially more sensitive molecular imaging tool for early detection and characterization of AD-related neurodegeneration variants at prodromal disease stages. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13195-021-00785-9.
format Online
Article
Text
id pubmed-7896407
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-78964072021-02-22 Data-driven FDG-PET subtypes of Alzheimer’s disease-related neurodegeneration Levin, Fedor Ferreira, Daniel Lange, Catharina Dyrba, Martin Westman, Eric Buchert, Ralph Teipel, Stefan J. Grothe, Michel J. Alzheimers Res Ther Research BACKGROUND: Previous research has described distinct subtypes of Alzheimer’s disease (AD) based on the differences in regional patterns of brain atrophy on MRI. We conducted a data-driven exploration of distinct AD neurodegeneration subtypes using FDG-PET as a sensitive molecular imaging marker of neurodegenerative processes. METHODS: Hierarchical clustering of voxel-wise FDG-PET data from 177 amyloid-positive patients with AD dementia enrolled in the Alzheimer’s Disease Neuroimaging Initiative (ADNI) was used to identify distinct hypometabolic subtypes of AD, which were then further characterized with respect to clinical and biomarker characteristics. We then classified FDG-PET scans of 217 amyloid-positive patients with mild cognitive impairment (“prodromal AD”) according to the identified subtypes and studied their domain-specific cognitive trajectories and progression to dementia over a follow-up interval of up to 72 months. RESULTS: Three main hypometabolic subtypes were identified: (i) “typical” (48.6%), showing a classic posterior temporo-parietal hypometabolic pattern; (ii) “limbic-predominant” (44.6%), characterized by old age and a memory-predominant cognitive profile; and (iii) a relatively rare “cortical-predominant” subtype (6.8%) characterized by younger age and more severe executive dysfunction. Subtypes classified in the prodromal AD sample demonstrated similar subtype characteristics as in the AD dementia sample and further showed differential courses of cognitive decline. CONCLUSIONS: These findings complement recent research efforts on MRI-based identification of distinct AD atrophy subtypes and may provide a potentially more sensitive molecular imaging tool for early detection and characterization of AD-related neurodegeneration variants at prodromal disease stages. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13195-021-00785-9. BioMed Central 2021-02-19 /pmc/articles/PMC7896407/ /pubmed/33608059 http://dx.doi.org/10.1186/s13195-021-00785-9 Text en © The Author(s) 2021 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Levin, Fedor
Ferreira, Daniel
Lange, Catharina
Dyrba, Martin
Westman, Eric
Buchert, Ralph
Teipel, Stefan J.
Grothe, Michel J.
Data-driven FDG-PET subtypes of Alzheimer’s disease-related neurodegeneration
title Data-driven FDG-PET subtypes of Alzheimer’s disease-related neurodegeneration
title_full Data-driven FDG-PET subtypes of Alzheimer’s disease-related neurodegeneration
title_fullStr Data-driven FDG-PET subtypes of Alzheimer’s disease-related neurodegeneration
title_full_unstemmed Data-driven FDG-PET subtypes of Alzheimer’s disease-related neurodegeneration
title_short Data-driven FDG-PET subtypes of Alzheimer’s disease-related neurodegeneration
title_sort data-driven fdg-pet subtypes of alzheimer’s disease-related neurodegeneration
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7896407/
https://www.ncbi.nlm.nih.gov/pubmed/33608059
http://dx.doi.org/10.1186/s13195-021-00785-9
work_keys_str_mv AT levinfedor datadrivenfdgpetsubtypesofalzheimersdiseaserelatedneurodegeneration
AT ferreiradaniel datadrivenfdgpetsubtypesofalzheimersdiseaserelatedneurodegeneration
AT langecatharina datadrivenfdgpetsubtypesofalzheimersdiseaserelatedneurodegeneration
AT dyrbamartin datadrivenfdgpetsubtypesofalzheimersdiseaserelatedneurodegeneration
AT westmaneric datadrivenfdgpetsubtypesofalzheimersdiseaserelatedneurodegeneration
AT buchertralph datadrivenfdgpetsubtypesofalzheimersdiseaserelatedneurodegeneration
AT teipelstefanj datadrivenfdgpetsubtypesofalzheimersdiseaserelatedneurodegeneration
AT grothemichelj datadrivenfdgpetsubtypesofalzheimersdiseaserelatedneurodegeneration
AT datadrivenfdgpetsubtypesofalzheimersdiseaserelatedneurodegeneration