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Cannabinoids and psychotic symptoms: A potential role for a genetic variant in the P2X purinoceptor 7 (P2RX7) gene.

Authors :
Boks MP
He Y
Schubart CD
Gastel WV
Elkrief L
Huguet G
Eijk KV
Vinkers CH
Kahn RS
Paus T
Conrod P
Hol EM
de Witte LD
Source :
Brain, behavior, and immunity [Brain Behav Immun] 2020 Aug; Vol. 88, pp. 573-581. Date of Electronic Publication: 2020 Apr 21.
Publication Year :
2020

Abstract

To investigate the biological mechanisms underlying the higher risk for psychosis in those that use cannabis, we conducted a genome-wide environment-interaction study (GWEIS). In a sample of individuals without a psychiatric disorder (N = 1262), we analyzed the interactions between regular cannabis use and genotype with psychotic-like experiences (PLE) as outcome. PLE were measured using the Community Assessment of Psychic Experiences (CAPE). The sample was enriched for those at the extremes of both cannabis use and PLE to increase power. A single nucleotide polymorphism in the P2RX7 gene (rs7958311) was associated with risk for a high level of psychotic experiences in regular cannabis users (p = 1.10 x10 <superscript>-7</superscript> ) and in those with high levels of lifetime cannabis use (p = 4.5 × 10 <superscript>-6</superscript> ). This interaction was replicated in individuals with high levels of lifetime cannabis use in the IMAGEN cohort (N = 1217, p = 0.020). Functional relevance of P2RX7 in cannabis users was suggested by in vitro experiments on activated monocytes. Exposure of these cells to tetrahydrocannabinol (THC) or cannabidiol (CBD) reduced the immunological response of the P2X7 receptor, which was dependent on the identified genetic variant. P2RX7 variants have been implicated in psychiatric disorders before and the P2X7 receptor is involved in pathways relevant to psychosis, such as neurotransmission, synaptic plasticity and immune regulation. We conclude that P2RX7 plays a role in vulnerability to develop psychotic symptoms when using cannabis and point to a new pathway that can potentially be targeted by newly developed P2X7 antagonists.<br /> (Copyright © 2020. Published by Elsevier Inc.)

Details

Language :
English
ISSN :
1090-2139
Volume :
88
Database :
MEDLINE
Journal :
Brain, behavior, and immunity
Publication Type :
Academic Journal
Accession number :
32330591
Full Text :
https://doi.org/10.1016/j.bbi.2020.04.051