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Bridging the Gap: Multi-Omics Profiling of Brain Tissue in Alzheimer's Disease and Older Controls in Multi-Ethnic Populations.

Authors :
Reddy JS
Heath L
Vander Linden A
Allen M
de Paiva Lopes K
Seifar F
Wang E
Ma Y
Poehlman WL
Quicksall ZS
Runnels A
Wang Y
Duong DM
Yin L
Xu K
Modeste ES
Shantaraman A
Dammer EB
Ping L
Oatman SR
Scanlan J
Ho C
Carrasquillo MM
Atik M
Yepez G
Mitchell AO
Nguyen TT
Chen X
Marquez DX
Reddy H
Xiao H
Seshadri S
Mayeux R
Prokop S
Lee EB
Serrano GE
Beach TG
Teich AF
Haroutunian V
Fox EJ
Gearing M
Wingo A
Wingo T
Lah JJ
Levey AI
Dickson DW
Barnes LL
De Jager P
Zhang B
Bennett D
Seyfried NT
Greenwood AK
Ertekin-Taner N
Source :
BioRxiv : the preprint server for biology [bioRxiv] 2024 Apr 20. Date of Electronic Publication: 2024 Apr 20.
Publication Year :
2024

Abstract

Introduction: Multi-omics studies in Alzheimer's disease (AD) revealed many potential disease pathways and therapeutic targets. Despite their promise of precision medicine, these studies lacked African Americans (AA) and Latin Americans (LA), who are disproportionately affected by AD.<br />Methods: To bridge this gap, Accelerating Medicines Partnership in AD (AMP-AD) expanded brain multi-omics profiling to multi-ethnic donors.<br />Results: We generated multi-omics data and curated and harmonized phenotypic data from AA (n=306), LA (n=326), or AA and LA (n=4) brain donors plus Non-Hispanic White (n=252) and other (n=20) ethnic groups, to establish a foundational dataset enriched for AA and LA participants. This study describes the data available to the research community, including transcriptome from three brain regions, whole genome sequence, and proteome measures.<br />Discussion: Inclusion of traditionally underrepresented groups in multi-omics studies is essential to discover the full spectrum of precision medicine targets that will be pertinent to all populations affected with AD.<br />Competing Interests: Conflict of interest statement The authors declare no conflicts of interest. Author disclosures are available in the supporting information.

Details

Language :
English
ISSN :
2692-8205
Database :
MEDLINE
Journal :
BioRxiv : the preprint server for biology
Accession number :
38659743
Full Text :
https://doi.org/10.1101/2024.04.16.589592