Psychological structure and neuroendocrine patterns of daily stress appraisals

Threat and challenge are two fundamental appraisal concepts of psychological stress theories, determined by the mismatch between demands and resources. Previous research has predominantly investigated the neuroendocrine correlates of stress appraisal in laboratory contexts during acute demanding situations. We tested whether the psychoneuroendocrinology of stress appraisals can also be investigated in naturalistic trans-contextual everyday life settings. Forty-two participants produced five daily saliva samples and provided concurrent questionnaire data on subjective stress, demands, resources, and the threat-challenge continuum over the course of five days (69% female; mean age = 22.8, range = 18-30 years). Momentary salivary cortisol and alpha amylase were predicted with three-level autoregressive linear mixed models. We found that both momentary cortisol and alpha amylase were elevated during higher subjective stress. In contrast, cortisol was not significantly related to a bipolar threat-challenge indicator. Moreover within-person response surface analyses showed no effect of the mismatch between demands and resources on either physiological stress indicator, but confirmed theoretically proposed effects on subjective threat-challenge, which was replicated in another intensive longitudinal (N = 61) and a large cross-sectional sample (N = 1194). In sum, our study (a) suggests robust relations between subjective stress and HPA/SAM axis activity on a moment-to-moment basis and (b) confirms theoretical predictions concerning stress appraisal and the mismatch between demands and resources on a psychological level. In contrast, no neuroendocrine patterns of threat-challenge were found, suggesting that neuroendocrine patterns might be context-specific and do not apply to a general demand-resource imbalance in everyday life. (DIPF/Orig.

No evidence for intervention-associated DNA methylation changes in monocytes of patients with posttraumatic stress disorder

DNA methylation patterns can be responsive to environmental influences. This observation has sparked interest in the potential for psychological interventions to influence epigenetic processes. Recent studies have observed correlations between DNA methylation changes and therapy outcome. However, most did not control for changes in cell composition. This study had two aims: first, we sought to replicate therapy-associated changes in DNA methylation of commonly assessed candidate genes in isolated monocytes from 60 female patients with post-traumatic stress disorder (PTSD). Our second, exploratory goal was to identify novel genomic regions with substantial pre-to-post intervention DNA methylation changes by performing whole-genome bisulfite sequencing (WGBS) in two patients with PTSD. Equivalence testing and Bayesian analyses provided evidence against physiologically meaningful intervention-associated DNA methylation changes in monocytes of PTSD patients in commonly investigated target genes (NR3C1, FKBP5, SLC6A4, OXTR). Furthermore, WGBS yielded only a limited set of candidate regions with suggestive evidence of differential DNA methylation pre- to post-therapy. These differential DNA methylation patterns did not prove replicable when investigated in the entire cohort. We conclude that there is no evidence for major, recurrent intervention-associated DNA methylation changes in the investigated genes in monocytes of patients with PTSD

No evidence for intervention-associated DNA methylation changes in monocytes of patients with posttraumatic stress disorder.

DNA methylation patterns can be responsive to environmental influences. This observation has sparked interest in the potential for psychological interventions to influence epigenetic processes. Recent studies have observed correlations between DNA methylation changes and therapy outcome. However, most did not control for changes in cell composition. This study had two aims: first, we sought to replicate therapy-associated changes in DNA methylation of commonly assessed candidate genes in isolated monocytes from 60 female patients with post-traumatic stress disorder (PTSD). Our second, exploratory goal was to identify novel genomic regions with substantial pre-to-post intervention DNA methylation changes by performing whole-genome bisulfite sequencing (WGBS) in two patients with PTSD. Equivalence testing and Bayesian analyses provided evidence against physiologically meaningful intervention-associated DNA methylation changes in monocytes of PTSD patients in commonly investigated target genes (NR3C1, FKBP5, SLC6A4, OXTR). Furthermore, WGBS yielded only a limited set of candidate regions with suggestive evidence of differential DNA methylation pre- to post-therapy. These differential DNA methylation patterns did not prove replicable when investigated in the entire cohort. We conclude that there is no evidence for major, recurrent intervention-associated DNA methylation changes in the investigated genes in monocytes of patients with PTSD

The DNA methylation landscape of the human oxytocin receptor gene (OXTR): data-driven clusters and their relation to gene expression and childhood adversity.

The oxytocin receptor gene (OXTR) is of interest when investigating the effects of early adversity on DNA methylation. However, there is heterogeneity regarding the selection of the most promising CpG sites to target for analyses. The goal of this study was to determine functionally relevant clusters of CpG sites within the OXTR CpG island in 113 mother-infant dyads, with 58 of the mothers reporting childhood maltreatment (CM). OXTR DNA methylation was analyzed in peripheral/umbilical blood mononuclear cells. Different complexity reduction approaches were used to reduce the 188 CpG sites into clusters of co-methylated sites. Furthermore, associations between OXTR DNA methylation (cluster- and site-specific level) and OXTR gene expression and CM were investigated in mothers. Results showed that, first, CpG sections differed strongly regarding their statistical utility for research of individual differences in DNA methylation. Second, cluster analyses and Partial Least Squares (PLS) suggested two clusters consisting of intron1/exon2 and the protein-coding region of exon3, respectively, as most strongly associated with outcome measures. Third, cross-validated PLS regression explained 7% of variance in CM, with low cross-validated variance explained for the prediction of gene expression. Fourth, substantial mother-child correspondence was observed in correlation patterns within the identified clusters, but only modest correspondence outside these clusters. This study makes an important contribution to the mapping of the DNA methylation landscape of the OXTR CpG island by highlighting clusters of CpG sites that show desirable statistical properties and predictive value. We provide a Companion Web Application to facilitate the choice of CpG sites

Demand-Resource Imbalance

R analysis scripts and supplements for the manuscript: "Psychological structure and neuroendocrine patterns of daily stress appraisals" (Sicorello et al., 2021

Sexuelle und physische Viktimisierungserfahrungen von Studierenden im Kontext fester Beziehungen, Dates und One-Night-Stands

Anhand einer Online-Befragung wurde die Prävalenz sexueller und physischer Viktimisierung in der Studienzeit differenziert nach den Kategorien feste Beziehung, Date und One-Night-Stand an einer Stichprobe 167 männlicher und weiblicher Studierender der Universität Mainz (Befragungszeitraum: Juli 2014). Die Gewalterfahrungen wurden in zwei Schweregraden erfasst. Von den Befragten berichteten 41,1 % minderschwere und 8,9 % schwere Gewalterfahrungen. Während die Prävalenz sexueller Viktimisierung für Studentinnen signifikant höher war, gab für beide Schweregrade ein höherer Prozentsatz männlicher Teilnehmer an, körperliche Gewalt erfahren zu haben. Minderschwere Gewalterfahrungen kamen generell am häufigsten in festen Beziehungen, schwere sexuelle Gewalterfahrungen am häufigsten bei Dates vor. Der Zusammenhang zwischen Viktimisierungserfahrungen in verschiedenen Beziehungstypen war moderat bis hoch. Am stärksten war die Assoziation sexueller Viktimisierung zwischen Dates und One-Night-Stands. Obwohl durch den geringen Stichprobenumfang nur bedingt von generalisierbaren Ergebnissen ausgegangen werden kann, ähneln die Prävalenzen denen anderer Studien. Die Ergebnisse legen demnach u. a. nahe, Dates als Risikosituationen sexueller Viktimisierung zu untersuchen

Highs and lows. Genetic susceptibility to daily events

Why people differ in their susceptibility to external events is essential to our understanding of personality, human development, and mental disorders. Genes explain a substantial portion of these differences. Specifically, genes influencing the serotonin system are hypothesized to be differential susceptibility factors, determining a person\u27s reactivity to both positive and negative environments. We tested whether genetic variation in the serotonin transporter (5-HTTLPR) is a differential susceptibility factor for daily events. Participants (N = 326, 77% female, mean age = 25, range = 17-36) completed smartphone questionnaires four times a day over four to five days, measuring stressors, uplifts, positive and negative affect. Affect was predicted from environment valence in the previous hour on a within-person level using three-level autoregressive linear mixed models. The 5-HTTLPR fulfilled all criteria of a differential susceptibility factor: Positive affect in carriers of the short allele (S) was less reactive to both uplifts and stressors, compared to homozygous carriers of the long allele (L/L). This pattern might reflect relative affective inflexibility in S-allele carriers. Our study provides insight into the serotonin system\u27s general role in susceptibility and highlights the need to assess the whole spectrum of naturalistic experiences. (DIPF/Orig.