Department of Biomedicine - Pharmacology and Therapeutics Unit, Faculty of Medicine, University of Porto, Porto, Portugal.
Department of Biomedicine - Pharmacology and Therapeutics Unit, Faculty of Medicine, University of Porto, Porto, Portugal; Department of Psychiatry and Mental Health, University Hospital Center of São João, Porto, Portugal.
Pharmacol Res. 2022 Jul;181:106258. doi: 10.1016/j.phrs.2022.106258. Epub 2022 May 16.
Cannabis sativa is a recreational drug commonly consumed in Europe and is getting popularity for both recreational and therapeutic use. In some individuals, the use of cannabis leads to psychotic disorders. This systematic review summarizes the current evidence linking genetic polymorphisms and inter-individual susceptibility to psychosis induced by cannabis.
Studies published from 2005 to 2020 were identified through Medline using PubMed, Web of Science and Scopus database and searches were conducted according to PRISMA guidelines. Initial search was performed with terms: "cannabis induced psychosis" AND "genetics".
From the initial group of 108 papers, 18 studies met our inclusion criteria. Many of the findings revealed associations with genetic polymorphisms modulations of genes involved directly (COMT, DRD2 and DAT) or indirectly (AKT1) to dopamine pathways. The most consistent finding was with COMT rs4680, where the presence of the Val allele was associated with a higher risk for cannabis-induced psychosis. This higher susceptibility was also reported for AKT1 (rs2494732) with the CC genotype. Of note, the only genome-wide association study identified a significant signal close to the cholinergic receptor muscarinic 3 represented by rs115455482 and rs74722579 predisposing to cannabis-induced hallucinations and remarkably no dopaminergic target was found.
Actual evidence supports the role of dopamine in cannabis induced psychosis. However, most of genetic polymorphism studies have as a starting point the pre-existing dopaminergic theoretical basis for psychosis. This alerts to the importance of more broad genetic studies. Integrate genetic results into biological systems may enhance our knowledge of cannabis induced psychosis and could help in the prevention and treatment of these patients.
大麻是一种在欧洲被广泛滥用的消遣性药物,它正在成为消遣和治疗用途的热门选择。在一些个体中,大麻的使用会导致精神障碍。本系统综述总结了目前的证据,这些证据将大麻引起的精神障碍与遗传多态性和个体易感性联系起来。
通过 Medline 使用 PubMed、Web of Science 和 Scopus 数据库进行了 2005 年至 2020 年期间发表的研究的检索,并根据 PRISMA 指南进行了搜索。初始搜索使用了以下术语:“大麻引起的精神障碍”和“遗传学”。
从最初的 108 篇论文中,有 18 项研究符合我们的纳入标准。许多研究结果表明,与基因直接(COMT、DRD2 和 DAT)或间接(AKT1)参与多巴胺途径的基因的遗传多态性调节有关。最一致的发现是 COMT rs4680,携带 Val 等位基因的个体发生大麻引起的精神障碍的风险更高。AKT1(rs2494732)的 CC 基因型也报告了这种更高的易感性。值得注意的是,唯一的全基因组关联研究确定了一个显著的信号,靠近胆碱能受体毒蕈碱 3,由 rs115455482 和 rs74722579 代表,易感性增加与大麻引起的幻觉有关,而且没有发现多巴胺能靶点。
现有证据支持多巴胺在大麻引起的精神障碍中的作用。然而,大多数遗传多态性研究都是以精神障碍的现有多巴胺理论基础为起点。这提醒我们需要进行更广泛的遗传研究。将遗传结果整合到生物系统中可以增强我们对大麻引起的精神障碍的认识,并有助于预防和治疗这些患者。