Background. Resting-state fMRI (rs-fMRI) co-activation patterns (CAPs) capture recurrent whole-brain states that may index neurobiological substrates of affective psychopathology, yet whether their dynamics co-evolve with symptom severity over the long-term course of depression and anxiety remains unknown. Methods. We analyzed rs-fMRI and clinical data from 340 participants in the NESDA cohort (228 with a depressive and/or anxiety disorder, AFF) at baseline (Y0), 2-year (Y2), and 9-year (Y9) follow-up. Four CAPs were identified and validated. CAP dwell time and entries were related to depression (IDS), anxiety (BAI), and fear (FQ) severity between subjects and within individuals. Results. At baseline, attention-somatomotor (AT-SMCAP) dwell time was inversely associated with depression severity in CTR (rho = -0.29, q < 0.05) but not AFF (rho = 0.09, q = 0.79). Longitudinally, group-level trajectories showed no CAP-symptom coupling; it emerged only within individuals, where increases in frontoparietal-default-mode (FP-DMCAP) dwell time tracked worsening depression in AFF only (Y2 to Y9: rho = 0.47, q < 0.01). Conclusions. AT-SMCAP distinguished health from illness cross-sectionally, whereas FP-DMCAP indexed illness course within individuals, effects not captured by group-averaged analyses. These findings highlight individual-level CAP dynamics as relevant to longitudinal brain-symptom coupling, with implications for precision psychiatry.
DMPFC-somatomotor connectivity is longitudinally associated with cognitive performance in early psychosis, suggesting a novel, reliable target for intervention for cognitive deficits in early psychosis.
K. A. Mignondje, J. Connolly, A. Beermann et al.· medRxiv· 0 citations
Baseline cortical morphometric features were associated with clinical and cognitive changes following antidepressant treatment in MDD, and single-ROI LOOCV models based on left cuneus and left SFC FD showed cross-validated associations with symptom improvement.
Background Adolescence is a critical window for autonomic and limbic development and a period of elevated risk for depression. Although autonomic and limbic system function have, independently, been linked to depression, they are coupled and both influenced by early life stress (ELS). We do not yet know, however, wheth...
Eugenia Giampetruzzi, C. Antonacci, Jean Rachel Bahk et al.· Neurobiology of Stress· 0 citations
Worry is an important contributor to anxiety and depressive disorders, particularly in adolescence. Underlying changes in brain networks are thought to drive development of pathological worry, yet the degree to which neural correlates of worry vary by age is unknown. Here, we use multivariate pattern analysis (MVPA) to...
Cecilia A. Westbrook, H. Karim, C. Andreescu et al.· medRxiv· 0 citations
BACKGROUND
Borderline Personality Disorder (BPD) involves affective instability, impaired emotion regulation, and self-injurious behavior, often linked to childhood adversity. Although prefrontal and insular abnormalities have been reported, the relationship between structural and functional changes in BPD is not well...
Vera Flasbeck, Björn Enzi, Georg Juckel et al.· European Archives of Psychia...· 0 citations
Findings indicate that individual variations in habenula-centered circuits are partly shaped by gene polymorphisms related to mood and circadian regulation and contribute to the symptom heterogeneity of depression.
M. Kim, J.-Y. Jung, S.-J. Cho et al.· International Journal of Neu...· 0 citations
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