Telomere length and mitochondrial DNA copy number in association with trauma-focused psychotherapy efficacy

Abstract

Early life adversities (ELA) have been linked to a greater risk for major depressive disorder (MDD) and treatment-resistant depression (TRD). The molecular mechanisms underlying the link between ELA and MDD and/or TRD are yet unknown. It has been suggested that ELA induces an allostatic burden, which in turn promotes oxidative stress and an inflammatory response that are further intensified by the influence of maladaptive coping behaviour. In this study we explored the role of two markers of cellular aging and oxidative stress (telomere length (TL) and mitochondrial DNA copy number mtDNAcn) in TRD and in response to trauma-focused psychotherapies. The study comprised 30 TRD patients receiving trauma-focused psychotherapies and 65 healthy controls. TL and mtDNAcn were measured at baseline and four weeks after the end of the psychotherapy sessions. Response was defined based on reduction in the Montgomery-Åsberg Depression Rating Scale (MADRS). In the case control analysis, the logistic regression model showed that mtDNAcn but not TLT was a significant predictor of diagnosis (chi-square 92.108, p=7.72e-20; contribution of mtDNAcn, B=-9-297, p=0.00009, Table 2). In the TRD sample, LTL and mtDNAcn were inversely correlated with MADRS score at baseline (TL, Pearson’s r=-0.478, p=0.008; mtDNAcn, Pearson’s r=-0.656, p=0.00008), but there was no difference in either TL or mtDNAcn between responders and non-responders. In conclusion, our findings support an involvement of cellular aging in TRD, and suggest that TLA and mtDNAcn are not predictors or mediators of response to trauma-focused psychotherapies.