Department of Psychiatry, Washington University School of Medicine, St Louis, MO, USA.
Department of Biomedicine-Human Genetics and Centre for Integrative Sequencing, Aarhus University, Aarhus, Denmark; The Lundbeck Foundation Initiative for Integrative Psychiatric Research, iPSYCH, Aarhus, Denmark; Center for Genomics and Personalized Medicine, Aarhus, Denmark.
Lancet Psychiatry. 2020 Dec;7(12):1032-1045. doi: 10.1016/S2215-0366(20)30339-4. Epub 2020 Oct 20.
Variation in liability to cannabis use disorder has a strong genetic component (estimated twin and family heritability about 50-70%) and is associated with negative outcomes, including increased risk of psychopathology. The aim of the study was to conduct a large genome-wide association study (GWAS) to identify novel genetic variants associated with cannabis use disorder.
To conduct this GWAS meta-analysis of cannabis use disorder and identify associations with genetic loci, we used samples from the Psychiatric Genomics Consortium Substance Use Disorders working group, iPSYCH, and deCODE (20 916 case samples, 363 116 control samples in total), contrasting cannabis use disorder cases with controls. To examine the genetic overlap between cannabis use disorder and 22 traits of interest (chosen because of previously published phenotypic correlations [eg, psychiatric disorders] or hypothesised associations [eg, chronotype] with cannabis use disorder), we used linkage disequilibrium score regression to calculate genetic correlations.
We identified two genome-wide significant loci: a novel chromosome 7 locus (FOXP2, lead single-nucleotide polymorphism [SNP] rs7783012; odds ratio [OR] 1·11, 95% CI 1·07-1·15, p=1·84 × 10) and the previously identified chromosome 8 locus (near CHRNA2 and EPHX2, lead SNP rs4732724; OR 0·89, 95% CI 0·86-0·93, p=6·46 × 10). Cannabis use disorder and cannabis use were genetically correlated (r 0·50, p=1·50 × 10), but they showed significantly different genetic correlations with 12 of the 22 traits we tested, suggesting at least partially different genetic underpinnings of cannabis use and cannabis use disorder. Cannabis use disorder was positively genetically correlated with other psychopathology, including ADHD, major depression, and schizophrenia.
These findings support the theory that cannabis use disorder has shared genetic liability with other psychopathology, and there is a distinction between genetic liability to cannabis use and cannabis use disorder.
National Institute of Mental Health; National Institute on Alcohol Abuse and Alcoholism; National Institute on Drug Abuse; Center for Genomics and Personalized Medicine and the Centre for Integrative Sequencing; The European Commission, Horizon 2020; National Institute of Child Health and Human Development; Health Research Council of New Zealand; National Institute on Aging; Wellcome Trust Case Control Consortium; UK Research and Innovation Medical Research Council (UKRI MRC); The Brain & Behavior Research Foundation; National Institute on Deafness and Other Communication Disorders; Substance Abuse and Mental Health Services Administration (SAMHSA); National Institute of Biomedical Imaging and Bioengineering; National Health and Medical Research Council (NHMRC) Australia; Tobacco-Related Disease Research Program of the University of California; Families for Borderline Personality Disorder Research (Beth and Rob Elliott) 2018 NARSAD Young Investigator Grant; The National Child Health Research Foundation (Cure Kids); The Canterbury Medical Research Foundation; The New Zealand Lottery Grants Board; The University of Otago; The Carney Centre for Pharmacogenomics; The James Hume Bequest Fund; National Institutes of Health: Genes, Environment and Health Initiative; National Institutes of Health; National Cancer Institute; The William T Grant Foundation; Australian Research Council; The Virginia Tobacco Settlement Foundation; The VISN 1 and VISN 4 Mental Illness Research, Education, and Clinical Centers of the US Department of Veterans Affairs; The 5th Framework Programme (FP-5) GenomEUtwin Project; The Lundbeck Foundation; NIH-funded Shared Instrumentation Grant S10RR025141; Clinical Translational Sciences Award grants; National Institute of Neurological Disorders and Stroke; National Heart, Lung, and Blood Institute; National Institute of General Medical Sciences.
大麻使用障碍的易感性具有很强的遗传成分(双胞胎和家庭遗传度约为 50-70%),与负面结果相关,包括精神病理学风险增加。本研究的目的是进行大规模全基因组关联研究(GWAS),以确定与大麻使用障碍相关的新遗传变异。
为了进行这项大麻使用障碍的 GWAS 荟萃分析,并确定与遗传位点的关联,我们使用了来自精神药理学基因组学联盟物质使用障碍工作组、iPSYCH 和 deCODE 的样本(总共 20916 例病例样本,363116 例对照样本),将大麻使用障碍病例与对照进行对比。为了研究大麻使用障碍与 22 个感兴趣的特征(选择这些特征是因为先前发表的表型相关性[例如,精神障碍]或假设的与大麻使用障碍的关联[例如,睡眠类型])之间的遗传重叠,我们使用连锁不平衡得分回归计算遗传相关性。
我们确定了两个全基因组显著的位点:一个新的 7 号染色体位点(FOXP2,主要单核苷酸多态性[SNP]rs7783012;优势比[OR]1.11,95%置信区间[CI]1.07-1.15,p=1.84×10)和先前确定的 8 号染色体位点(靠近 CHRNA2 和 EPHX2,主要 SNP rs4732724;OR 0.89,95%CI 0.86-0.93,p=6.46×10)。大麻使用障碍和大麻使用具有遗传相关性(r=0.50,p=1.50×10),但它们与我们测试的 22 个特征中的 12 个具有显著不同的遗传相关性,这表明大麻使用和大麻使用障碍至少具有部分不同的遗传基础。大麻使用障碍与其他精神病理学呈正相关,包括 ADHD、重度抑郁症和精神分裂症。
这些发现支持大麻使用障碍与其他精神病理学具有共同遗传易感性的理论,并且大麻使用与大麻使用障碍之间存在遗传易感性的区别。
美国国立卫生研究院;美国国家酒精滥用和酒精中毒研究所;美国国家药物滥用研究所;基因组学和个性化医学与整合测序中心;欧盟地平线 2020 计划;美国国家儿童健康与人类发育研究所;新西兰健康研究理事会;美国国家老龄化研究所;英国惠康信托基金会病例对照研究联盟;英国研究与创新部医学研究理事会(英国研究与创新部);大脑与行为研究基金会;美国国立耳聋和其他交流障碍研究所;物质滥用和心理健康服务管理局;美国国立生物医学成像和生物工程研究所;澳大利亚国家健康与医学研究理事会;加州大学与边缘型人格障碍相关的疾病研究计划 2018 年 NARSAD 青年研究员赠款;全国儿童健康研究基金会(治愈儿童);坎特伯雷医学研究基金会;新西兰彩票委员会;奥塔哥大学;Carney 基因组学中心;詹姆斯·休姆遗赠基金;美国国立卫生研究院:基因、环境与健康倡议;美国国立卫生研究院;美国国家癌症研究所;威廉 T 格兰特基金会;澳大利亚研究理事会;弗吉尼亚烟草和解基金会;美国退伍军人事务部第 1 和第 4 号精神病学研究、教育和临床中心;第 5 框架计划(FP-5)GenomEUtwin 项目;丹麦隆德基金会;美国国立卫生研究院资助的共享仪器拨款 S10RR025141;临床转化科学奖;美国国立神经疾病与中风研究所;美国国家心肺血液研究所;美国国立普通医学科学研究所。