{"title":"Association Between Cannabis Use and Neuropsychiatric Disorders: A Two-sample Mendelian Randomization Study.","authors":"Wei Guo, Lin Dong, Qingxing Lu, Mengtong Xie, Yuqi Yang, Yanchi Zhang, Xiaoyu Lu, Qiong Yu","doi":"10.31083/AP46108","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>The progressive legalization and widespread use of cannabis has led to its use as a treatment for certain neuropsychiatric disorders. Traditional epidemiological studies suggest that cannabis use has an effect on some neurocognitive aspects. However, it is unclear whether cannabis use is causally related to common neuropsychiatric disorders. The present study was conducted to illustrate the causal relationships of genetically predicted cannabis use with common neuropsychiatric disorders.</p><p><strong>Methods: </strong>We used a two-sample Mendelian randomization method using genome-wide association study (GWAS) summary statistics obtained from publicly available databases on lifetime cannabis use and 10 neuropsychiatric disorders, including multiple sclerosis (MS), Alzheimer's disease (AD), amyotrophic lateral sclerosis (ALS), autism spectrum disorder (ASD), epilepsy, generalized epilepsy, focal epilepsy, migraine, migraine with aura, migraine without aura, schizophrenia (SCZ), anorexia nervosa (AN), attention-deficit/hyperactivity disorder (ADHD), and Parkinson's disease (PD) were studied with a two-sample Mendelian randomization method for GWAS summary statistics. The inverse variance weighted (IVW) method was used as the main analysis model.</p><p><strong>Results: </strong>Our study suggests that lifetime cannabis use is associated with an increased risk of developing PD (odds ratio (OR) = 1.782; 95% CI 1.032-3.075; <i>p</i> = 0.038) and an increased risk of ADHD in female participants (OR = 1.650; 95% CI 1.051-2.590; <i>p</i> = 0.029).</p><p><strong>Conclusions: </strong>Cannabis intake may cause adverse effects relating to certain neuropsychiatric disorders. Therefore, special attention should be paid to the side effects of addictive drugs during clinical treatment to avoid harmful effects on the brain and neurocognition.</p>","PeriodicalId":72151,"journal":{"name":"Alpha psychiatry","volume":"26 4","pages":"46108"},"PeriodicalIF":3.5000,"publicationDate":"2025-08-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12416058/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Alpha psychiatry","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.31083/AP46108","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/8/1 0:00:00","PubModel":"eCollection","JCR":"Q3","JCRName":"PSYCHIATRY","Score":null,"Total":0}
引用次数: 0
Abstract
Background: The progressive legalization and widespread use of cannabis has led to its use as a treatment for certain neuropsychiatric disorders. Traditional epidemiological studies suggest that cannabis use has an effect on some neurocognitive aspects. However, it is unclear whether cannabis use is causally related to common neuropsychiatric disorders. The present study was conducted to illustrate the causal relationships of genetically predicted cannabis use with common neuropsychiatric disorders.
Methods: We used a two-sample Mendelian randomization method using genome-wide association study (GWAS) summary statistics obtained from publicly available databases on lifetime cannabis use and 10 neuropsychiatric disorders, including multiple sclerosis (MS), Alzheimer's disease (AD), amyotrophic lateral sclerosis (ALS), autism spectrum disorder (ASD), epilepsy, generalized epilepsy, focal epilepsy, migraine, migraine with aura, migraine without aura, schizophrenia (SCZ), anorexia nervosa (AN), attention-deficit/hyperactivity disorder (ADHD), and Parkinson's disease (PD) were studied with a two-sample Mendelian randomization method for GWAS summary statistics. The inverse variance weighted (IVW) method was used as the main analysis model.
Results: Our study suggests that lifetime cannabis use is associated with an increased risk of developing PD (odds ratio (OR) = 1.782; 95% CI 1.032-3.075; p = 0.038) and an increased risk of ADHD in female participants (OR = 1.650; 95% CI 1.051-2.590; p = 0.029).
Conclusions: Cannabis intake may cause adverse effects relating to certain neuropsychiatric disorders. Therefore, special attention should be paid to the side effects of addictive drugs during clinical treatment to avoid harmful effects on the brain and neurocognition.
背景:大麻的逐步合法化和广泛使用已导致其用于治疗某些神经精神疾病。传统的流行病学研究表明,大麻的使用对某些神经认知方面有影响。然而,目前尚不清楚大麻的使用是否与常见的神经精神疾病有因果关系。目前的研究是为了说明遗传预测大麻使用与常见神经精神疾病的因果关系。方法:我们采用双样本孟德尔随机化方法,利用全基因组关联研究(GWAS)从公开数据库中获得的终身大麻使用和10种神经精神疾病的汇总统计数据,包括多发性硬化症(MS)、阿尔茨海默病(AD)、肌萎缩侧索硬化症(ALS)、自闭症谱系障碍(ASD)、癫痫、全身性癫痫、局灶性癫痫、偏头痛、先兆偏头痛、无先兆偏头痛、精神分裂症(SCZ)、神经性厌食症(AN)、采用GWAS汇总统计的双样本孟德尔随机化方法对注意缺陷/多动障碍(ADHD)和帕金森病(PD)进行研究。采用方差反加权法(IVW)作为主要分析模型。结果:我们的研究表明,终生使用大麻与患帕金森病的风险增加有关(优势比(OR) = 1.782;95% ci 1.032-3.075;p = 0.038),女性参与者患ADHD的风险增加(OR = 1.650; 95% CI 1.051-2.590; p = 0.029)。结论:大麻摄入可能导致与某些神经精神疾病相关的不良反应。因此,在临床治疗中应特别注意成瘾性药物的副作用,避免对大脑和神经认知产生有害影响。