Study register · detail
Mixed
GRADE
Low
33 citations
Samplen = 310 Pat.
Duration4 years
EndpointDepressive symptoms
Blindingn.a.
DesignLongitudinale Kohortenstudie
Key finding
Cannabis use increases depressive symptoms only in genetically vulnerable adolescents (5-HTTLPR short allele), not in all.
Summary
Longitudinal cohort study (n=310 adolescents, 4 years) on cannabis use and depressive symptoms. Parallel growth model: cannabis use increases the risk of an increase in depressive symptoms over time, but exclusively in carriers of the short allele of the 5-HTTLPR genotype (p<0.05 after covariate control). Effect confirmed in sibling replication sample. No evidence for reverse causality (depression → cannabis).
P
PopulationAdolescents, n=310 (plus replication with younger siblings), longitudinal over 4 years
I
InterventionCannabis use (naturalistically assessed, course over time)
O
OutcomeCannabis use increases the risk of an increase in depressive symptoms over time, but only in carriers of the short allele of the 5-HTTLPR genotype (significant after controlling for covariates; replicated in sibling sample)
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
Evidence for the assumption that cannabis use is associated with depression and depressive symptoms is inconsistent and mostly weak. It is likely that the mixed results are due to the fact that prior studies ignored the moderating effects of an individual's genetic vulnerability. The present study takes a first step in scrutinizing the relationship between cannabis use and depressive symptoms by taking a developmental molecular-genetic perspective. Specifically, we concentrated on changes in cannabis use and depressive symptoms over time in a simultaneous manner and differences herein for individuals with and without the short allele of the 5-hydroxytryptamine (serotonin) transporter gene-linked polymorphic region (5-HTTLPR) genotype. Data were from 310 adolescents over a period of 4 years. We used a parallel-process growth model, which allows co-development of cannabis use and depressive symptoms throughout adolescence, and the possible role of the 5-HTTLPR genotype in this process. We used data from the younger siblings of these adolescents in an attempt to replicate potential findings. The parallel-process growth model shows that cannabis use increases the risk for an increase in depressive symptoms over time but only in the presence of the short allele of the 5-HTTLPR genotype. This effect remained significant after controlling for covariates. We did not find conclusive support for the idea that depressive symptoms affect cannabis use. These findings were replicated in the sample of the younger siblings. The findings of the present study show first evidence that the links between cannabis use and depressive symptoms are conditional on the individual's genetic makeup.
The impediment to action advances action.