Department of Psychiatry, UMC Utrecht Brain Center, University Medical Centre Utrecht, Utrecht University, The Netherlands.
Department of Psychiatry, Tergooi Hospital, Blaricum, The Netherlands.
Brain Behav Immun. 2020 Aug;88:573-581. doi: 10.1016/j.bbi.2020.04.051. Epub 2020 Apr 21.
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) and in those with high levels of lifetime cannabis use (p = 4.5 × 10). 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.
为了探究大麻使用与精神病风险增加相关的生物学机制,我们进行了一项全基因组环境互作研究(GWEIS)。在一个无精神障碍个体样本(N=1262)中,我们分析了大麻使用的规律性与基因型与类精神病体验(PLE)之间的交互作用作为结果。PLE 使用社区心理体验评估量表(CAPE)进行测量。样本中包含了大麻使用和 PLE 处于极端的个体,以增加研究的效力。P2RX7 基因(rs7958311)中的单核苷酸多态性与规律性大麻使用者的高水平精神病体验风险相关(p=1.10×10),以及与终生高大麻使用水平相关(p=4.5×10)。在 IMAGEN 队列中具有终生高大麻使用水平的个体中复制了这种交互作用(N=1217,p=0.020)。体外激活单核细胞实验表明 P2RX7 在大麻使用者中的功能相关性。这些细胞暴露于四氢大麻酚(THC)或大麻二酚(CBD)会降低 P2X7 受体的免疫反应,这依赖于所鉴定的遗传变异。P2RX7 变异与精神障碍有关,P2X7 受体参与与精神病相关的途径,如神经递质、突触可塑性和免疫调节。我们得出结论,P2RX7 在使用大麻时易发生精神病症状,这表明 P2RX7 可能成为新开发的 P2X7 拮抗剂的潜在靶点。