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Updated: Jun 24, 2026

Brain Morphology of Cannabis Users With or Without Psychosis: A Pilot MRI Study
Published on: August 18, 2020
Systematic Review and Meta-analysis: Prevalence, Correlates, and Impact of Cannabis Use and Cannabis Use Disorder in
Gonzalo Salazar de Pablo1, Nuria Laherran-Cantera2, Claudia Aymerich3
1Institute of Psychiatry, Psychology & Neuroscience (IoPPN), King's College London, United Kingdom; Child and Adolescent Mental Health Services, South London and Maudsley (SLaM) NHS Foundation Trust, London, United Kingdom; Institute of Psychiatry and Mental Health, Hospital General Universitario Gregorio Marañón School of Medicine, Universidad Complutense, IiSGM, CIBERSAM, Madrid, Spain; Biobizkaia Health Research Institute, Basque Country University, Basurto University Hospital, OSI Bilbao-Basurto, Centro de Investigación en Red de Salud Mental (CIBERSAM), Instituto de Salud Carlos III, Barakaldo, Bizkaia, Spain.
Objective:
To quantify prevalence of cannabis use (CU) and cannabis use disorder (CUD) in early-onset psychosis (EOP) (age <18) and examine their correlates and clinical and functional impact.
Method:
This systematic review and meta-analysis searched 6 databases until July 1, 2025, for studies evaluating CU/CUD in EOP. Data were extracted by independent researchers, and quality assessment was conducted using the Newcastle-Ottawa Scale. Heterogeneity, publication bias, subgroup, and meta-regression analyses were performed, followed by a narrative synthesis.
Results:
Forty studies (N = 3,473; mean [SD] age = 16.2 [1.6] years; 59% male) were included. In EOP, pooled prevalence was 32.8% (95% CI 18.5-51.2) for current CU, 40.2% (95% CI 31.3-49.7) for lifetime CU, and 36.6% (95% CI 18.2-59.9) for lifetime CUD. In meta-regression analyses, current CU was associated with male sex (β = .012, p = .021) and hospitalization rates (β = .006, p = .021), but with less severe negative symptoms (β = -.191, p = .001) and lower proportion of schizophrenia diagnosis (β = -.026, p = .049). Lifetime CU was associated with cocaine use (β = .101, p = .003) and less severe negative symptoms (β = -.173, p = .030). Narrative synthesis indicated that CU commonly preceded psychosis onset and was linked to negative outcomes (eg, longer duration of untreated psychosis and higher hospitalization rates) in EOP. Study quality was mostly fair (67.5%); Grading of Recommendations Assessment, Development and Evaluation certainty ranged from low to moderate.
Conclusion:
CU and CUD are common in individuals with EOP and relate to clinical presentation. Screening and integrated substance use care should be embedded in primary care and clinical settings. Further longitudinal studies and randomized clinical trials to evaluate the efficacy of interventions to reduce CU and CUD are needed.
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