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Fröhlich, A.S.* ; Gerstner, N. ; Gagliardi, M.* ; Ködel, M.* ; Yusupov, N.* ; Matosin, N.* ; Czamara, D.* ; Sauer, S.* ; Roeh, S.* ; Murek, V.* ; Chatzinakos, C.* ; Daskalakis, N.P.* ; Knauer-Arloth, J. ; Ziller, M.J.* ; Binder, E.B.*

Single-nucleus transcriptomic profiling of human orbitofrontal cortex reveals convergent effects of aging and psychiatric disease.

Nat. Neurosci. 27, 2021-2032 (2024)
Verlagsversion DOI PMC
Open Access Hybrid
Creative Commons Lizenzvertrag
Aging is a complex biological process and represents the largest risk factor for neurodegenerative disorders. The risk for neurodegenerative disorders is also increased in individuals with psychiatric disorders. Here, we characterized age-related transcriptomic changes in the brain by profiling ~800,000 nuclei from the orbitofrontal cortex from 87 individuals with and without psychiatric diagnoses and replicated findings in an independent cohort with 32 individuals. Aging affects all cell types, with LAMP5+LHX6+ interneurons, a cell-type abundant in primates, by far the most affected. Disrupted synaptic transmission emerged as a convergently affected pathway in aged tissue. Age-related transcriptomic changes overlapped with changes observed in Alzheimer's disease across multiple cell types. We find evidence for accelerated transcriptomic aging in individuals with psychiatric disorders and demonstrate a converging signature of aging and psychopathology across multiple cell types. Our findings shed light on cell-type-specific effects and biological pathways underlying age-related changes and their convergence with effects driven by psychiatric diagnosis.
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Publikationstyp Artikel: Journalartikel
Dokumenttyp Wissenschaftlicher Artikel
Schlagwörter Gene-expression; Quantile Normalization; Bioconductor Package; Alzheimers-disease; Brain; Age; Neurodegeneration; Association; Microglia; Lingo-1
Sprache englisch
Veröffentlichungsjahr 2024
HGF-Berichtsjahr 2024
ISSN (print) / ISBN 1097-6256
e-ISSN 1546-1726
Zeitschrift Nature Neuroscience
Quellenangaben Band: 27, Heft: 10, Seiten: 2021-2032 Artikelnummer: , Supplement: ,
Verlag Nature Publishing Group
Verlagsort Heidelberger Platz 3, Berlin, 14197, Germany
Begutachtungsstatus Peer reviewed
Institut(e) Institute of Computational Biology (ICB)
POF Topic(s) 30205 - Bioengineering and Digital Health
Forschungsfeld(er) Enabling and Novel Technologies
PSP-Element(e) G-503800-001
Förderungen National Institute of Alcohol Abuse and Alcoholism of the National Institutes of Health
Hope for Depression Research Foundation
BMBF eMED program grant DINGS
Alexander von Humboldt Foundation
Joachim Herz Foundation - Else-Kroener-Fresenius Foundation
Brain & Behavior Research Foundation
National Institute of Mental Health
New South Wales Brain Tissue Resource Centre at the University of Sydney
University of Sydney
Nathalie Gerstner is supported by the Joachim Herz Foundation.
DOI 10.1038/s41593-024-01742-z
WOS ID 001304673100001
Scopus ID 85203165419
PubMed ID 39227716
Erfassungsdatum 2024-10-14
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