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Carrie E. Bearden

2 papers in the library · publishing 2024

Papers

Assessing evidence supporting cannabis harm reduction practices for adolescents at clinical high-risk for psychosis: a review and clinical implementation tool.

Psychological Medicine January 1, 2024 Simon Kapler, Laura Adery, Gil D Hoftman et al.

Cannabis use is linked to increased rates of psychotic disorders and worsening of symptoms in people with psychosis spectrum disorders, including those at Clinical High Risk for Psychosis (CHR-P). While causality remains uncertain, cannabis may be a modifiable risk factor for conversion to psychotic disorder in CHR-P individuals. Current evidence supports a harm reduction approach rather than abstinence alone: reducing frequency of use, choosing lower delta-9-tetrahydrocannabinol content or cannabidiol-only products, avoiding edibles with inconsistent potency, improving patient-provider communication about cannabis use and psychotic-like experiences, and using a collaborative, individualized therapeutic approach. Whether these interventions lower conversion risk is unknown.

Altered neurobehavioral reward response predicts psychotic-like experiences in youth exposed to cannabis prenatally

Carolyn M. Amir, Dara G. Ghahremani, Sarah E. Chang et al. preprint

Prenatal cannabis exposure is linked to psychotic-like experiences in youth, and this relationship may involve disrupted reward-related brain function. In a large longitudinal study of children aged 9–10 at baseline, those with prenatal cannabis exposure (652 children) showed blunted neural response to reward anticipation, which was associated with psychotic-like experiences and predicted psychosis symptoms in middle adolescence. Dampened behavioral reward sensitivity was also associated with psychotic-like experiences across follow-ups. Trait-level measures of reward motivation and impulsivity were more strongly linked to psychotic-like experiences in children with prenatal cannabis exposure. Blunted activation in reward-related brain regions may be a biomarker for increased psychosis risk.