Genetic and clinical correlates of two neuroanatomical AI dimensions in the Alzheimer's disease continuum.
Détails
ID Serval
serval:BIB_DCE3349227B3
Type
Article: article d'un périodique ou d'un magazine.
Collection
Publications
Institution
Titre
Genetic and clinical correlates of two neuroanatomical AI dimensions in the Alzheimer's disease continuum.
Périodique
Translational psychiatry
ISSN
2158-3188 (Electronic)
ISSN-L
2158-3188
Statut éditorial
Publié
Date de publication
05/10/2024
Peer-reviewed
Oui
Volume
14
Numéro
1
Pages
420
Langue
anglais
Notes
Publication types: Journal Article
Publication Status: epublish
Publication Status: epublish
Résumé
Alzheimer's disease (AD) is associated with heterogeneous atrophy patterns. We employed a semi-supervised representation learning technique known as Surreal-GAN, through which we identified two latent dimensional representations of brain atrophy in symptomatic mild cognitive impairment (MCI) and AD patients: the "diffuse-AD" (R1) dimension shows widespread brain atrophy, and the "MTL-AD" (R2) dimension displays focal medial temporal lobe (MTL) atrophy. Critically, only R2 was associated with widely known sporadic AD genetic risk factors (e.g., APOE ε4) in MCI and AD patients at baseline. We then independently detected the presence of the two dimensions in the early stages by deploying the trained model in the general population and two cognitively unimpaired cohorts of asymptomatic participants. In the general population, genome-wide association studies found 77 genes unrelated to APOE differentially associated with R1 and R2. Functional analyses revealed that these genes were overrepresented in differentially expressed gene sets in organs beyond the brain (R1 and R2), including the heart (R1) and the pituitary gland, muscle, and kidney (R2). These genes were enriched in biological pathways implicated in dendritic cells (R2), macrophage functions (R1), and cancer (R1 and R2). Several of them were "druggable genes" for cancer (R1), inflammation (R1), cardiovascular diseases (R1), and diseases of the nervous system (R2). The longitudinal progression showed that APOE ε4, amyloid, and tau were associated with R2 at early asymptomatic stages, but this longitudinal association occurs only at late symptomatic stages in R1. Our findings deepen our understanding of the multifaceted pathogenesis of AD beyond the brain. In early asymptomatic stages, the two dimensions are associated with diverse pathological mechanisms, including cardiovascular diseases, inflammation, and hormonal dysfunction-driven by genes different from APOE-which may collectively contribute to the early pathogenesis of AD. All results are publicly available at https://labs-laboratory.com/medicine/ .
Mots-clé
Humans, Alzheimer Disease/genetics, Alzheimer Disease/pathology, Male, Female, Cognitive Dysfunction/genetics, Cognitive Dysfunction/pathology, Aged, Genome-Wide Association Study, Atrophy, Brain/pathology, Magnetic Resonance Imaging, Temporal Lobe/pathology, Aged, 80 and over, Apolipoprotein E4/genetics, Middle Aged
Pubmed
Web of science
Open Access
Oui
Création de la notice
11/10/2024 13:34
Dernière modification de la notice
31/10/2024 7:13