Multi‐Omics analysis identifies that different genetic perturbations affect various molecular mechanisms underlying Alzheimer's Disease (AD) in an age‐dependent manner

We have characterized in vivo signatures of three genetic candidates for late-onset Alzheimer's disease (LOAD), identifying alterations in specific LOAD-related pathways for each variant. Our study highlights that assembling multi-omics measurements reveals interrelated pathway alterations in Alzheimer's Disease (AD) and enables the identification of biomarker combinations that may inform clinical practice. Our approach provides a platform for further exploration into the causes and progression of AD by assessing animal models at different ages and/or with different combinations of LOAD risk variants.

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Publication Details

Journal
Alzheimer s & Dementia
Published
2025-12-01
DOI
https://doi.org/10.1002/alz70855_096942
Primary Topic
Alzheimer's disease research and treatments
Type
article
Field-Weighted Citation Impact
0.00
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article

Multi‐Omics analysis identifies that different genetic perturbations affect various molecular mechanisms underlying Alzheimer's Disease (AD) in an age‐dependent manner

D Garceau, Carolyn Paisie, Catrina Spruce, Michael Sasner et al.
Alzheimer s & Dementia
Alzheimer's disease research and treatments
article

Multi‐Omics analysis identifies that different genetic perturbations affect various molecular mechanisms underlying Alzheimer's Disease (AD) in an age‐dependent manner

D Garceau, Carolyn Paisie, Catrina Spruce, Michael Sasner, Ravi S. Pandey, Gareth R Howell, Anantharaman Shantaraman, Kevin P Kotredes, Bruce T. Lamb, Duc M Duong, Claudia Rangel‐Barajas, Adrian L Oblak, Gregory W Carter, Nicholas T. Seyfried
article en

Abstract

We have characterized in vivo signatures of three genetic candidates for late-onset Alzheimer's disease (LOAD), identifying alterations in specific LOAD-related pathways for each variant. Our study highlights that assembling multi-omics measurements reveals interrelated pathway alterations in Alzheimer's Disease (AD) and enables the identification of biomarker combinations that may inform clinical practice. Our approach provides a platform for further exploration into the causes and progression of AD by assessing animal models at different ages and/or with different combinations of LOAD risk variants.

Alzheimer s & DementiaVol. 21(S1)
Emory University (US), Neurosciences Institute (US), Jackson Laboratory (US), Indiana University School of Medicine, Indiana University – Purdue University Indianapolis (US)
Openalex Percentile: Top 34%
Alzheimer's disease research and treatments
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