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大麻使用障碍与其他物质使用特征之间的遗传影响和因果途径。

Genetic influences and causal pathways shared between cannabis use disorder and other substance use traits.

机构信息

Department of Psychiatry, Yale University School of Medicine, New Haven, CT, USA.

Veterans Affairs Connecticut Healthcare System, West Haven, CT, USA.

出版信息

Mol Psychiatry. 2024 Sep;29(9):2905-2910. doi: 10.1038/s41380-024-02548-y. Epub 2024 Apr 5.

Abstract

Cannabis use disorder (CanUD) has increased with the legalization of the use of cannabis. Around 20% of individuals using cannabis develop CanUD, and the number of users has grown with increasing ease of access. CanUD and other substance use disorders (SUDs) are associated phenotypically and genetically. We leveraged new CanUD genomics data to undertake genetically-informed analyses with unprecedented power, to investigate the genetic architecture and causal relationships between CanUD and lifetime cannabis use with risk for developing SUDs and substance use traits. Analyses included calculating local and global genetic correlations, genomic structural equation modeling (genomicSEM), and Mendelian Randomization (MR). Results from the genetic correlation and genomicSEM analyses demonstrated that CanUD and cannabis use differ in their relationships with SUDs and substance use traits. We found significant causal effects of CanUD influencing all the analyzed traits: opioid use disorder (OUD) (Inverse variant weighted, IVW β = 0.925 ± 0.082), problematic alcohol use (PAU) (IVW β = 0.443 ± 0.030), drinks per week (DPW) (IVW β = 0.182 ± 0.025), Fagerström Test for Nicotine Dependence (FTND) (IVW β = 0.183 ± 0.052), cigarettes per day (IVW β = 0.150 ± 0.045), current versus former smokers (IVW β = 0.178 ± 0.052), and smoking initiation (IVW β = 0.405 ± 0.042). We also found evidence of bidirectionality showing that OUD, PAU, smoking initiation, smoking cessation, and DPW all increase risk of developing CanUD. For cannabis use, bidirectional relationships were inferred with PAU, smoking initiation, and DPW; cannabis use was also associated with a higher risk of developing OUD (IVW β = 0.785 ± 0.266). GenomicSEM confirmed that CanUD and cannabis use load onto different genetic factors. We conclude that CanUD and cannabis use can increase the risk of developing other SUDs. This has substantial public health implications; the move towards legalization of cannabis use may be expected to increase other kinds of problematic substance use. These harmful outcomes are in addition to the medical harms associated directly with CanUD.

摘要

大麻使用障碍(CanUD)随着大麻使用合法化而增加。大约 20%的使用大麻的个体出现 CanUD,并且随着获取途径的增加,使用者的数量也在增加。CanUD 和其他物质使用障碍(SUDs)在表型和遗传上相关。我们利用新的 CanUD 基因组学数据,利用前所未有的强大力量进行遗传信息分析,以研究 CanUD 与终生大麻使用与发展 SUDs 和物质使用特征的风险之间的遗传结构和因果关系。分析包括计算局部和全局遗传相关性、基因组结构方程建模(genomicSEM)和孟德尔随机化(MR)。遗传相关性和基因组 SEM 分析的结果表明,CanUD 和大麻使用在与 SUDs 和物质使用特征的关系上存在差异。我们发现 CanUD 对所有分析特征都有显著的因果影响:阿片类药物使用障碍(OUD)(逆变异加权,IVW β=0.925±0.082)、有问题的酒精使用(PAU)(IVW β=0.443±0.030)、每周饮酒量(DPW)(IVW β=0.182±0.025)、尼古丁依赖 Fagerström 测试(FTND)(IVW β=0.183±0.052)、每天吸烟量(IVW β=0.150±0.045)、当前吸烟者与 former 吸烟者(IVW β=0.178±0.052)和吸烟开始(IVW β=0.405±0.042)。我们还发现了双向性的证据,表明 OUD、PAU、吸烟开始、戒烟和 DPW 都会增加发展 CanUD 的风险。对于大麻使用,在 PAU、吸烟开始和 DPW 中推断出双向关系;大麻使用也与更高的 OUD 发展风险相关(IVW β=0.785±0.266)。基因组 SEM 证实,CanUD 和大麻使用加载到不同的遗传因素上。我们得出结论,CanUD 和大麻使用可以增加发展其他 SUDs 的风险。这具有重大的公共卫生意义;大麻使用合法化的趋势可能会增加其他种类的有问题的物质使用。这些有害后果除了直接与 CanUD 相关的医疗危害之外。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4813/11420056/7d2880242337/41380_2024_2548_Fig1_HTML.jpg

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