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. 2019 Jun;29(6):786-794.
doi: 10.1016/j.euroneuro.2019.04.005. Epub 2019 May 7.

Gene-environment interaction between an endocannabinoid system genetic polymorphism and cannabis use in first episode of psychosis

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Gene-environment interaction between an endocannabinoid system genetic polymorphism and cannabis use in first episode of psychosis

Miquel Bioque et al. Eur Neuropsychopharmacol. 2019 Jun.

Abstract

Alterations of the endocannabinoid system (ECS) may play an important role in the development of schizophrenia and other psychotic disorders. Cannabis use is one of the environmental factors more repeatedly related to an increase the risk of developing a psychotic episode, while its use modifies the ECS normal function. In the present study we purposed to examine the gene by environment (GxE) interaction between 15 selected single nucleotide polymorphisms (SNPs) related to the ECS and cannabis use in a cohort of 321 patients with a first episode of psychosis (FEP) and 241 matched healthy controls. We found the fatty-acid amide hydrolase (FAAH) rs2295633 SNP genetic polymorphism was associated with a greater risk of presenting a FEP in subjects with relevant cannabis use, but not in subjects without a history of cannabis use. The probability of presenting a FEP was tenfold higher (OR: 10.69) in cannabis users who were homozygote carriers of the T allele of the FAAH rs2295633 SNP, compared to users of cannabis without this genotype. We also found that a higher a proportion of TT carriers of the FAAH rs2295633 SNP with a positive history of cannabis use was treated with high potency antipsychotic. This study has identified a GxE-environment interaction between a genetic polymorphism from the ECS and cannabis use involved in the risk of presenting a FEP. Although this preliminary data should be replicated with independent samples, our results highlight the importance of the pro-psychotic effects of exogenous cannabis use over the ECS in certain subjects.

Keywords: Cannabis; Endocannabinoid system; FAAH; Psychosis; Schizophrenia; rs2295633.

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