Study register · detail
Mixed
GRADE
Low
55 citations
Samplen = 596 Pat.
DurationFollow-up until the 22nd year…
EndpointPsychotic symptoms
Blindingn.a.
DesignProspektive Längsschnittstudie (Kohorte)
Key finding
Prenatal cannabis exposure and early age of onset increase the risk of psychotic symptoms, whereby the mediation pathway via EAOM was not significant.
Summary
Prospective cohort study (n=596): early age of onset of cannabis use (EAOM) significantly predicted increased rates of psychotic symptoms in young adulthood (22 years) (p<0,05). In addition, prenatal cannabis exposure (PME) predicted EAOM, suggesting an indirect developmental risk pathway from the prenatal phase to young adulthood.
P
PopulationYoung adults (offspring from prenatal cohort, n=596, age 22 years) with and without prenatal cannabis exposure
I
InterventionPrenatal cannabis exposure (PME) and early age of onset of cannabis use (EAOM)
O
OutcomePME and EAOM significantly predicted increased rates of psychotic symptoms at age 22; direct effect of PME on PS marginally significant (p=0,06) after adjustment; total effect (direct + indirect) significant
Confidence in the evidence
Low
The second of four GRADE levels, the effect estimate is of limited reliability.
Quality profile
Sample size
★★★★★
Blinding
—
Effect size
Mixed
Citations / year
★★★★★
Authors
Share
Abstract
<h4>Background</h4>Studies have demonstrated that an early age of onset of Cannabis use (EAOM) is associated with a higher risk of developing psychotic symptoms (PS) compared to initiating Cannabis use at a later age or not at all. Research has also found that prenatal Cannabis exposure (PME) predicts EAOM. This report evaluates the relationships among PME, EAOM, and PS.<h4>Method</h4>Subjects were initially interviewed in their fourth prenatal month. Women and offspring who completed the birth assessment (n = 763) were selected for follow-up. Women and their offspring were followed until the offspring were 22 years of age: 596 offspring were evaluated. At age 22, PS were assessed in the offspring with the Diagnostic Interview Schedule using DSM-IV criteria. Analyses controlled for significant covariates including other prenatal substance exposures, race, gender, and offspring substance use at 22 years.<h4>Results</h4>PME and EAOM significantly predicted increased rates of PS at 22 years controlling for other significant covariates. The direct effect of PME on PS was marginally significant (p = 0.06) when EAOM was entered into the model and other covariates were fixed. In the mediation analysis, EAOM did not significantly mediate the association between PME and PS, controlling for significant covariates, nor was the indirect pathway significant when structural equation modeling was used. The total effect of the direct and indirect pathways was significant.<h4>Conclusions</h4>In addition to EAOM, PME may also play a role in the association between Cannabis use and the development of PS. This could highlight a new area for prevention.
The impediment to action advances action.