Blood mRNA Expression in Alzheimer's Disease and Dementia With Lewy Bodies.


Journal

The American journal of geriatric psychiatry : official journal of the American Association for Geriatric Psychiatry
ISSN: 1545-7214
Titre abrégé: Am J Geriatr Psychiatry
Pays: England
ID NLM: 9309609

Informations de publication

Date de publication:
09 2022
Historique:
received: 31 08 2021
revised: 01 02 2022
accepted: 03 02 2022
pubmed: 15 3 2022
medline: 10 8 2022
entrez: 14 3 2022
Statut: ppublish

Résumé

The objective of this study was to investigate the expression of genes in Alzheimer's disease (AD) and dementia with Lewy bodies (DLB), both at the mild cognitive impairment (MCI) and dementia stages, to improve our understanding of disease pathophysiology and investigate the potential for diagnostic and prognostic biomarkers based on mRNA expression. Cross-sectional observational study. University research center. People with MCI with Lewy bodies (MCI-LB, n=55), MCI-AD (n=19), DLB (n=38), AD (n=24) and a cognitively unimpaired comparison group (n=28). Ribonucleic acid sequencing of whole blood. Differentially expressed genes (DEGs) were identified and gene set enrichment analysis was carried out. Compared with the cognitively unimpaired group, there were 22 DEGs in MCI-LB/DLB and 61 DEGs in MCI-AD/AD. DEGS were also identified when comparing the two disease groups. Expression of ANP32A was associated with more rapid cognitive decline in MCI-AD/AD. Gene set enrichment analysis identified downregulation in gene sets including MYC targets and oxidative phosphorylation in MCI-LB/DLB; upregulation of immune and inflammatory responses in MCI-AD/AD; and upregulation of interferon-α and -γ responses in MCI-AD/AD compared with MCI-LB/DLB. This study identified multiple DEGs in MCI-LB/DLB and MCI-AD/AD. One of these DEGs, ANP32A, may be a prognostic marker in AD. Genes related to mitochondrial function were downregulated in MCI-LB/DLB. Previously reported upregulation of genes associated with inflammation and immune responses in MCI-AD/AD was confirmed in this cohort. Differences in interferon responses between MCI-AD/AD and MCI-LB/DLB suggest that there are key differences in peripheral immune responses between these diseases.

Identifiants

pubmed: 35283023
pii: S1064-7481(22)00264-0
doi: 10.1016/j.jagp.2022.02.003
pii:
doi:

Substances chimiques

ANP32A protein, human 0
Nuclear Proteins 0
RNA, Messenger 0
RNA-Binding Proteins 0

Types de publication

Journal Article Observational Study Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

964-975

Subventions

Organisme : Department of Health
Pays : United Kingdom

Informations de copyright

Copyright © 2022 The Authors. Published by Elsevier Inc. All rights reserved.

Auteurs

Paul C Donaghy (PC)

Translational and Clinical Research Institute (PCD, DE, DK, JPT, CMM, AJT), Newcastle University, Newcastle upon Tyne, United Kingdom. Electronic address: paul.donaghy@ncl.ac.uk.

Simon J Cockell (SJ)

School of Biomedical, Nutrition and Sports Sciences (SJC), Newcastle University, Newcastle upon Tyne, United Kingdom.

Carmen Martin-Ruiz (C)

Biosciences Institute (CMR, JC), Newcastle University, Newcastle upon Tyne, United Kingdom.

Jonathan Coxhead (J)

Biosciences Institute (CMR, JC), Newcastle University, Newcastle upon Tyne, United Kingdom.

Joseph Kane (J)

Centre for Public Health (JK), Queen's University Belfast, Belfast, United Kingdom.

Daniel Erskine (D)

Translational and Clinical Research Institute (PCD, DE, DK, JPT, CMM, AJT), Newcastle University, Newcastle upon Tyne, United Kingdom.

David Koss (D)

Translational and Clinical Research Institute (PCD, DE, DK, JPT, CMM, AJT), Newcastle University, Newcastle upon Tyne, United Kingdom.

John-Paul Taylor (JP)

Translational and Clinical Research Institute (PCD, DE, DK, JPT, CMM, AJT), Newcastle University, Newcastle upon Tyne, United Kingdom.

Christopher M Morris (CM)

Translational and Clinical Research Institute (PCD, DE, DK, JPT, CMM, AJT), Newcastle University, Newcastle upon Tyne, United Kingdom.

John T O'Brien (JT)

Department of Psychiatry (JTO), University of Cambridge, Cambridge, United Kingdom.

Alan J Thomas (AJ)

Translational and Clinical Research Institute (PCD, DE, DK, JPT, CMM, AJT), Newcastle University, Newcastle upon Tyne, United Kingdom.

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Classifications MeSH