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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...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2021
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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 |
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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 |
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