Sex and pubertal stage as moderators of the association between resting-state connectivity of striatal circuitry and reward sensitivity in the Adolescent Brain Cognitive Development study
Altered reward sensitivity (either heightened or blunted) has been observed in a range of psychiatric disorders. Understanding neurodevelopmental pathways associated with individual differences in reward sensitivity will therefore help inform prevention and intervention efforts for a range of disorders. In this Registered Report, we used data from the Adolescent Brain Cognitive Development℠ study (ABCD study®), from the baseline, 2-year follow-up, and 4-year follow-up waves of data collection, when participants were on average aged 10, 12, and 14 years old, respectively, to examine these pathways using resting-state functional magnetic resonance imaging. Our aims were to examine whether striatal connectivity with the default mode network and cingulo-opercular network were associated with individual differences in reward sensitivity, and whether effects differed by sex and pubertal stage. Results indicated that reward sensitivity was positively associated with ventral striatum connectivity with the default mode network and negatively associated with ventral striatum connectivity with the cingulo-opercular network. In addition, adolescents with higher connectivity between the dorsal striatum (the caudate and putamen) and the cingulo-opercular network exhibited greater declines in reward sensitivity with pubertal development. Overall, increased striatal connectivity with the cingulo-opercular network may be associated with decreased reward sensitivity due to heightened regulation of reward-related function by the cingulo-opercular network, which plays a role in self-regulation and cognitive control.
The findings suggest that the level of pubertal maturation is associated with the longitudinal stability of large-scale brain networks in girls, and a subnetwork positively associated with Tanner breast stage is identified.
Susumu Morita, K. Kasai, Masahiro Kiyota et al.· Neurosciences research· 0 citations
BACKGROUND
Variation in pubertal maturation relative to same-age, same-sex peers (pubertal timing) has been linked to increased risk for depressive symptoms during adolescence. This developmental period is also characterized by substantial reorganization of functional brain networks. However, how pubertal timing relate...
Athanasia Metoki, B. Kay, R. Chauvin et al.· Biological Psychiatry: Cogni...· 0 citations
A sex-specific pattern within the dopaminergic pathways may underlie the clinical divergences between male and female patients with Parkinson’s disease (PD) over the disease course. One hundred forty-seven drug-naive PD patients and 38 controls were enrolled. Anatomical and rs-fMRI images were acquired at baseline. C...
R. de Micco, S. Satolli, Noemi Piramide et al.· npj Parkinson's Disease· 0 citations
Investigation of magnetic resonance imaging-derived neurodevelopmental cortical brain Age Gap Estimate and adverse life events as risk factors of early cannabis initiation suggest that while cortical brainAGE may be somewhat increase vulnerability to adolescent cannabis use in females, its contributions are modest at b...
K. Thiessen, Y. Yu, L. Schmid et al.· medRxiv· 0 citations
Associations between patterns of brain connectivity and brain structural features have transdiagnostic relevance to psychopathology. There is considerable evidence for disruptions to the hippocampus and temporoparietal brain systems in psychotic disorders. The present study examines structure–function relationships—spe...
K. Aberizk, B. Ku, Heng-Yi Cao et al.· Brain Structure and Function· 0 citations
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 limite...
Paula M. Henneberg, Katja Beesdo-Baum, M. Marxen et al.· Translational Psychiatry· 0 citations
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