Please use this identifier to cite or link to this item: http://hdl.handle.net/1942/48166
Title: Whole blood mitochondrial DNA copy number in depressed patients with and without a history of adverse childhood experiences: the role of blood cell composition
Authors: de Punder, Karin
Entringer, Sonja
MARTENS, Dries 
Karabatsiakis, Alexander
Kipka, Bilbo
Heim, Christine
Deuter, Christian E.
Otte, Christian
Wingenfeld, Katja
Kuehl, Linn K.
Issue Date: 2026
Publisher: 
Source: The world journal of biological psychiatry,
Status: Early view
Abstract: Objectives Adverse childhood experiences (ACE) are a significant risk factor for developing major depressive disorder (MDD) later in life, with mitochondria, key sensors of biological stress signals, emerging as a potential underlying mechanism. In the present study, we investigated the effects of ACE and MDD on whole blood mitochondrial DNA copy number (mtDNAcn), a proposed biomarker of mitochondrial health. In our analyses, we accounted for the platelet-to-leukocyte ratio, recognised as a source of variation in mtDNAcn measurements. Methods Whole blood mtDNAcn was measured by qPCR in n = 21 healthy participants without ACE, n = 25 MDD patients without ACE, n = 22 healthy participants with ACE, n = 23 patients with MDD and ACE. None of the participants was taking psychotropic medication. Results We observed a significant effect of ACE on whole blood mtDNAcn, while no effect of MDD or ACE and MDD interaction was seen. After adjustment for the platelet-to-leukocyte ratio, the effect of ACE on mtDNAcn was no longer significant. Conclusions Our findings do not support an association between ACE or MDD and whole blood mtDNAcn. Considering blood cell composition may enhance the understanding of whole blood mtDNAcn findings in trauma‑ and MDD‑related research.
Keywords: Adverse childhood experiences;biomarker research;major depressive disorder (MDD);mitochondrial DNA copy number (mtDNAcn);platelet-to-leukocyte ratio
Document URI: http://hdl.handle.net/1942/48166
ISSN: 1562-2975
e-ISSN: 1814-1412
DOI: 10.1080/15622975.2025.2601134
ISI #: WOS:001654323200001
Category: A1
Type: Journal Contribution
Appears in Collections:Research publications

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