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Open access Aug 2026

Fluctuations in real-life drinking in alcohol use disorder: A one-year longitudinal study using gamified tasks of decision making and cognitive control.

BACKGROUND Alcohol use disorder (AUD) is a major contributor to global disability and mortality. Cross-sectional studies have linked AUD to reduced cognitive control and heightened risky decision-making. However, the temporal direction of these effects remains unknown: are cognitive-behavioral alterations a consequence or a precursor of changes in drinking? METHODS We deployed a battery of smartphone-based, gamified tasks in a one-year longitudinal ecological momentary assessment study of N=603 participants diagnosed with mostly mild to moderate AUD. Tasks measured cognitive control (working memory, response inhibition) and decision-making (risk-taking, information sampling). Participants completed tasks monthly and reported alcohol consumption every two days. RESULTS We found that monthly fluctuations in aspects of decision-making predicted subsequent consumption. Specifically, participants shifted to higher monthly alcohol consumption when their risk-taking was higher in a mixed gambling context and lower in a loss context in the preceding month. Further, when information sampling biases decreased, participants consumed more alcohol in the subsequent month. This temporal direction-that within-subject fluctuations in task outcomes preceded changes in monthly drinking-was specific, was not observed vice versa and survived correction for autocorrelation in drinking, indicating risky decision-making as a precursor of subsequent drinking. Fluctuations in cognitive control and risk-taking in a win context were not associated with fluctuations in drinking. DISCUSSION Our findings offer novel insights into the cognitive-behavioral forces driving changes in alcohol consumption in AUD: specific decision-making alterations precede changes in consumption. These findings suggest that smartphone-based gamified tasks show promise to identify periods of heightened risk paving the way for mechanism-based, real-time interventions in AUD.

Hilmar Zech, Maria Waltmann, D. Reichert et al. · 0 citations
Open access Jul 2026

Changes in resting-state functional connectivity linked to affective symptoms: insights from a population-based study of adolescents and young adults

First episodes of affective disorders often emerge during adolescence and young adulthood. Alterations in resting-state functional connectivity (RSFC) have been reported in affective disorders, yet findings are heterogeneous and associations of RSFC with subclinical affective symptoms in community samples remain limited. A better understanding of these underlying neurobiological mechanisms may aid in identifying early vulnerability markers of affective disorders. We examined associations between affective symptom severity and both static and dynamic RSFC using resting-state fMRI data from 512 adolescents and young adults (aged 14–23) drawn from an age- and sex-stratified population-based sample. Group independent component analysis was used to derive RSFC measures. Associations with depressive and manic symptom severity were assessed while controlling for age and sex. Dynamic RSFC was analyzed using a sliding-window approach. Static RSFC showed significant effects of age and sex but no associations with affective symptoms. Dynamic RSFC analysis identified four connectivity states. In one state, manic symptom severity and its interaction with depressive symptom severity were associated with connectivity between the postcentral gyrus and the right superior temporal gyrus. Additionally, the dynamic index fraction of time showed interactions of affective symptoms with age and sex. Overall, RSFC measures demonstrated limited sensitivity to subclinical affective symptom variation in community youth, with only a single state-specific association observed. These findings suggest that subtle alterations in somatomotor-default mode network connectivity may reflect early vulnerability-related processes, though replications and further research are required. Key limitations include the use of very brief symptom measures and developmental heterogeneity across the sample.

Paula M. Henneberg, Katja Beesdo-Baum, M. Marxen et al. · 0 citations

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