Trans-ancestry epigenome-wide association meta-analysis of DNA methylation with lifetime cannabis use.

Fang Fang,Bryan Quach, Kaitlyn G Lawrence,Jenny van Dongen,Jesse A Marks, Sara Lundgren,Mingkuan Lin, Veronika V Odintsova,Ricardo Costeira, Zongli Xu,Linran Zhou,Meisha Mandal, Yujing Xia,Jacqueline M Vink,Laura J Bierut, Miina Ollikainen,Jack A Taylor, Jordana T Bell,Jaakko Kaprio, Dorret I Boomsma,Ke Xu,Dale P Sandler, Dana B Hancock,Eric O Johnson

Molecular psychiatry(2023)

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摘要
Cannabis is widely used worldwide, yet its links to health outcomes are not fully understood. DNA methylation can serve as a mediator to link environmental exposures to health outcomes. We conducted an epigenome-wide association study (EWAS) of peripheral blood-based DNA methylation and lifetime cannabis use (ever vs. never) in a meta-analysis including 9436 participants (7795 European and 1641 African ancestry) from seven cohorts. Accounting for effects of cigarette smoking, our trans-ancestry EWAS meta-analysis revealed four CpG sites significantly associated with lifetime cannabis use at a false discovery rate of 0.05 [Formula: see text]: cg22572071 near gene ADGRF1, cg15280358 in ADAM12, cg00813162 in ACTN1, and cg01101459 near LINC01132. Additionally, our EWAS analysis in participants who never smoked cigarettes identified another epigenome-wide significant CpG site, cg14237301 annotated to APOBR. We used a leave-one-out approach to evaluate methylation scores constructed as a weighted sum of the significant CpGs. The best model can explain 3.79% of the variance in lifetime cannabis use. These findings unravel the DNA methylation changes associated with lifetime cannabis use that are independent of cigarette smoking and may serve as a starting point for further research on the mechanisms through which cannabis exposure impacts health outcomes.
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dna methylation,lifetime cannabis use,meta-analysis meta-analysis,trans-ancestry,epigenome-wide
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