Lithium response in bipolar disorder: Epigenome-wide DNA methylation signatures and epigenetic aging

dc.contributor.author
González-Blanco, Leticia
dc.contributor.author
Bobes García, Julio
dc.contributor.author
Schulze, Thomas G.
dc.contributor.author
Vieta i Pascual, Eduard, 1963-
dc.contributor.author
Benabarre, Antonio
dc.contributor.author
Arias Sampériz, Bárbara
dc.contributor.author
Zafrilla-López, Marina 
dc.contributor.author
Acosta-Díez, Miriam
dc.contributor.author
Mitjans Niubó, Marina
dc.contributor.author
Giménez Palomo, Anna
dc.contributor.author
Saiz, Pilar A.
dc.contributor.author
Barrot i Feixat, Carme
dc.contributor.author
Jiménez Martínez, Ester
dc.contributor.author
Papiol, Sergi
dc.contributor.author
Ruiz, Victoria
dc.contributor.author
Gavín, Patrícia
dc.contributor.author
García-Portilla González, María Paz, 1962-
dc.date.accessioned
2026-01-21T13:22:43Z
dc.date.available
2026-01-21T13:22:43Z
dc.date.issued
2026-01-20T11:21:02Z
dc.date.issued
2026-01-20T11:21:02Z
dc.date.issued
2024-04-25
dc.date.issued
2026-01-20T11:21:02Z
dc.identifier
0924-977X
dc.identifier
https://hdl.handle.net/2445/225798
dc.identifier
748181
dc.identifier.uri
http://hdl.handle.net/2445/225798
dc.description.abstract
Lithium (Li) is the first-line treatment for bipolar disorder (BD) even though only 30 % of BD patients are considered excellent responders. The mechanisms by which Li exerts its action are not clearly understood, but it has been suggested that specific epigenetic mechanisms, such as methylation processes, may play a role. In this regard, DNA methylation patterns can be used to estimate epigenetic age (EpiAge), which is accelerated in BD patients and reversed by Li treatment. Our first aim was to compare the DNA methylation profile in peripheral blood between BD patients categorized as excellent responders to Li (Ex-Rp) and non-responders (N-Rp). Secondly, EpiAge was estimated to detect differential age acceleration between the two groups. A total of 130 differentially methylated positions (DMPs) and 16 differentially methylated regions (DMRs) between Ex-Rp (n = 26) and N-Rp (n = 37) were identified (FDR adjusted p-value < 0.05). We found 122 genes mapping the DMPs and DMRs, nine of which (HOXB6, HOXB3, HOXB-AS3, TENM2, CACNA1B, ANK3, EEF2K, CYP1A1, and SORCS2) had previously been linked to Li response. We found genes related to the GSK3β pathway to be highly represented. Using FUMA, we found enrichment in Gene Ontology Cell Component for the synapse. Gene network analysis highlighted functions related to the cell cycle, nervous system development and function, and gene expression. No significant differences in age acceleration were found between Ex-Rp and N-Rp for any of the epigenetic clocks analysed. Our findings indicate that a specific methylation pattern could determine the response to Li in BD patients. We also found that a significant portion of the differentially methylated genes are closely associated with the GSK3β pathway, reinforcing the role of this system in Li response. Future longitudinal studies with larger samples will help to elucidate the epigenetic mechanisms underlying Li response.
dc.format
87 p.
dc.format
application/pdf
dc.language
eng
dc.publisher
Elsevier B.V.
dc.relation
Versió postprint del document publicat a: https://doi.org/10.1016/j.euroneuro.2024.03.010
dc.relation
European Neuropsychopharmacology, 2024, vol. 85, p. 23-31
dc.relation
https://doi.org/10.1016/j.euroneuro.2024.03.010
dc.rights
cc-by-nc-nd (c) Elsevier B.V., 2024
dc.rights
http://creativecommons.org/licenses/by-nc-nd/4.0/
dc.rights
info:eu-repo/semantics/openAccess
dc.subject
Trastorn bipolar
dc.subject
Epigenètica
dc.subject
Liti
dc.subject
Manic-depressive illness
dc.subject
Epigenetics
dc.subject
Lithium
dc.title
Lithium response in bipolar disorder: Epigenome-wide DNA methylation signatures and epigenetic aging
dc.type
info:eu-repo/semantics/article
dc.type
info:eu-repo/semantics/acceptedVersion


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