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Meta-analysis identifies shared genetic loci between cannabis use and sleep disorders

Meta-analysis identifies shared genetic loci between cannabis use and sleep disorders
Photo by Ben Maffin / Unsplash
Key Takeaway
Consider the observational genetic links between cannabis use and sleep traits, but do not infer causality.

This is a meta-analysis using data from the All of Us and UK Biobank cohorts, comprising 152,807 cases and 220,272 controls, to investigate the genetic architecture linking cannabis use with sleep and circadian traits. The authors synthesized evidence to identify shared genetic loci and correlations.

The analysis identified 39 independent loci associated with both cannabis use and sleep/circadian rhythms. The authors reported significant positive genetic correlations between cannabis use and clinical insomnia, insomnia-related medication usage, and objectively measured nighttime physical activity. They also reported significant negative genetic correlations with morningness chronotype and daytime activity. Colocalization analysis showed near-perfect colocalization at the SLC39A8 and CADM2 loci between cannabis use and clinical insomnia.

The authors did not report effect sizes, p-values, or confidence intervals for these findings. The study is observational and cannot infer causality. Limitations were not explicitly reported in the provided data.

The practice relevance noted is investigating the genetic effects of cannabis use as its use becomes more widespread, both recreationally and medicinally. The findings suggest shared genetic pathways but require further validation.

Study Details

Study typeMeta analysis
EvidenceLevel 1
PublishedApr 2026
View Original Abstract ↓
Cannabis use is an increasingly common therapeutic for a variety of chronic diseases. In addition, people with sleep problems may self-medicate using cannabis products. However, genetic architecture of cannabis use and its shared genetic predispositions with sleep traits has not been systematically examined. We performed a meta-analysis of cannabis use within the All of Us and UK Biobank cohorts, consisting of 152,807 cases and 220,272 controls. Our meta-analysis identified 39 independent loci, including the previously reported CADM2 locus associated with cannabis use and replicating previous work. Additionally our associations include neuronal and sleep-regulating genes such as HTR1A, RAI1, SLC39A8, and NCAM1. Moreover, tissue-specific analyses revealed that the genetic architecture of cannabis use is heavily enriched within the central nervous system and specific brain cell types. In addition, we observed significant positive genetic correlations with clinical insomnia, insomnia-related medication usage, and objectively measured nighttime physical activity, alongside negative correlations with morningness chronotype and daytime activity. Fine-mapping and colocalization analyses identified shared genetic signals between cannabis use and clinical insomnia including a near-perfect colocalization at SLC39A8 and CADM2. Together, these results highlight the shared genetic risk between cannabis use and sleep disorders. Additionally, our findings indicate the importance of investigating the genetic effects of cannabis use as its use becomes more widespread, both recreationally and medicinally.
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