Dempster Emma L, Wong Chloe C Y, Burrage Joe, Hannon Eilis, Quattrone Diego, Trotta Giulia, Rodriguez Victoria, Alameda Luis, Spinazzola Edoardo, Tripoli Giada, Austin-Zimmerman Isabelle, Li Zhikun, Gayer-Anderson Charlotte, Freeman Tom P, Johnson Emma C, Jongsma Hannah E, Stilo Simona, La Cascia Caterina, Ferraro Laura, La Barbera Daniele, Lasalvia Antonio, Tosato Sarah, Tarricone Ilaria, D'Andrea Giuseppe, Galatolo Michela, Tortelli Andrea, Pompili Maurizio, Selten Jean-Paul, de Haan Lieuwe, Menezes Paulo Rossi, Del Ben Cristina M, Santos Jose Luis, Arrojo Manuel, Bobes Julio, Sanjuán Julio, Bernardo Miguel, Arango Celso, Jones Peter B, Breen Gerome, Mondelli Valeria, Dazzan Paola, Iyegbe Conrad, Vassos Evangelos, Morgan Craig, Mukherjee Diptendu, van Os Jim, Rutten Bart, O'Donovan Michael C, Sham Pak, Mill Jonathan, Murray Robin, Di Forti Marta
Department of Clinical & Biomedical Sciences, University of Exeter Medical School, University of Exeter, Exeter, UK.
Department of Social, Genetic and Developmental Psychiatry, Institute of Psychiatry, Psychology and Neuroscience, King's College London, London, UK.
Mol Psychiatry. 2025 Apr;30(4):1277-1286. doi: 10.1038/s41380-024-02689-0. Epub 2024 Oct 16.
The rising prevalence and legalisation of cannabis worldwide have underscored the need for a comprehensive understanding of its biological impact, particularly on mental health. Epigenetic mechanisms, specifically DNA methylation, have gained increasing recognition as vital factors in the interplay between risk factors and mental health. This study aimed to explore the effects of current cannabis use and high-potency cannabis on DNA methylation in two independent cohorts of individuals experiencing first-episode psychosis (FEP) compared to control subjects. The combined sample consisted of 682 participants (188 current cannabis users and 494 never users). DNA methylation profiles were generated on blood-derived DNA samples using the Illumina DNA methylation array platform. A meta-analysis across cohorts identified one CpG site (cg11669285) in the CAVIN1 gene that showed differential methylation with current cannabis use, surpassing the array-wide significance threshold, and independent of the tobacco-related epigenetic signature. Furthermore, a CpG site localised in the MCU gene (cg11669285) achieved array-wide significance in an analysis of the effect of high-potency (THC = > 10%) current cannabis use. Pathway and regional analyses identified cannabis-related epigenetic variation proximal to genes linked to immune and mitochondrial function, both of which are known to be influenced by cannabinoids. Interestingly, a model including an interaction term between cannabis use and FEP status identified two sites that were significantly associated with current cannabis use with a nominally significant interaction suggesting that FEP status might moderate how cannabis use affects DNA methylation. Overall, these findings contribute to our understanding of the epigenetic impact of current cannabis use and highlight potential molecular pathways affected by cannabis exposure.
全球范围内大麻流行率的上升及其合法化凸显了全面了解其生物学影响的必要性,尤其是对心理健康的影响。表观遗传机制,特别是DNA甲基化,作为风险因素与心理健康相互作用中的重要因素,已得到越来越多的认可。本研究旨在探讨当前使用大麻和高浓度大麻对两组独立的首发精神病(FEP)患者与对照受试者DNA甲基化的影响。合并样本包括682名参与者(188名当前大麻使用者和494名从未使用者)。使用Illumina DNA甲基化阵列平台对血液来源的DNA样本进行DNA甲基化谱分析。跨队列的荟萃分析在CAVIN1基因中鉴定出一个CpG位点(cg11669285),该位点显示出与当前大麻使用相关的差异甲基化,超过了全阵列显著性阈值,且独立于烟草相关的表观遗传特征。此外,在对高浓度(THC = > 10%)当前大麻使用影响的分析中,位于MCU基因中的一个CpG位点(cg11669285)达到了全阵列显著性。通路和区域分析确定了与免疫和线粒体功能相关基因附近的大麻相关表观遗传变异,已知这两者均受大麻素影响。有趣的是,一个包含大麻使用与FEP状态相互作用项的模型确定了两个与当前大麻使用显著相关的位点,具有名义上显著的相互作用,表明FEP状态可能会调节大麻使用对DNA甲基化的影响。总体而言,这些发现有助于我们理解当前大麻使用的表观遗传影响,并突出了受大麻暴露影响的潜在分子途径。