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利用基因组数据研究酒精、烟草、大麻和阿片类药物使用对生物和认知衰老的因果影响。

Leveraging Genomic Data to Examine the Causal Impact of Alcohol, Tobacco, Cannabis, and Opioid Use on Biological and Cognitive Ageing.

作者信息

Balbona Jared V, Jeffries Paul, Gorelik Aaron J, Nelson Elliot C, Bogdan Ryan, Agrawal Arpana, Johnson Emma C

机构信息

Department of Psychiatry, School of Medicine, Washington University in St. Louis, St. Louis, Missouri, USA.

Department of Psychological and Brain Sciences, Washington University in St. Louis, St. Louis, Missouri, USA.

出版信息

Addict Biol. 2025 Jul;30(7):e70066. doi: 10.1111/adb.70066.

DOI:10.1111/adb.70066
PMID:40653731
Abstract

Although substance use is associated with a shortened lifespan, impeded health and accelerated biological ageing, the factors contributing to the associations between substance use and ageing are poorly understood. We used summary statistics from genome-wide association studies (GWAS) to investigate whether substance involvement (N from 28K to 2M)-including alcohol, tobacco, cannabis and opioid use and use disorders-is genetically correlated with various ageing metrics (N from 162K to 2.7M) and whether these correlations reflect shared genetic etiologies or putative causal relationships. Using Linkage Disequilibrium Score Regression (LDSC), we found widespread evidence of genetic correlations between substance use/use disorders and indices of physical, cognitive and biological ageing. We then employed a series of Mendelian randomization-based approaches, finding significant causal effects of genetic predispositions to both tobacco use disorder and quantity of tobacco smoked on various markers of ageing. Causal effects of problematic alcohol use and cannabis use disorder were also found, though findings were mixed. Evidence of reverse causality (i.e., ageing causing substance use), meanwhile, was scant. Collectively, these results demonstrate strong triangulation across approaches and highlight the importance of integrating genetic insights into public health strategies for reducing the burden of SUDs across the lifespan.

摘要

尽管物质使用与寿命缩短、健康受损和生物衰老加速有关,但导致物质使用与衰老之间关联的因素却知之甚少。我们利用全基因组关联研究(GWAS)的汇总统计数据,来调查物质使用情况(样本量从2.8万到200万)——包括酒精、烟草、大麻和阿片类药物使用及其使用障碍——是否与各种衰老指标(样本量从16.2万到270万)存在遗传相关性,以及这些相关性是否反映了共同的遗传病因或假定的因果关系。使用连锁不平衡评分回归(LDSC),我们发现了物质使用/使用障碍与身体、认知和生物衰老指标之间存在遗传相关性的广泛证据。然后,我们采用了一系列基于孟德尔随机化的方法,发现烟草使用障碍的遗传易感性和吸烟量对各种衰老标志物均有显著的因果效应。还发现了有问题的酒精使用和大麻使用障碍的因果效应,不过结果不一。与此同时,反向因果关系(即衰老导致物质使用)的证据很少。总体而言,这些结果表明不同方法之间有很强的相互印证,并突出了将遗传见解纳入公共卫生策略以减轻一生中物质使用障碍负担的重要性。

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本文引用的文献

1
Global Healthspan-Lifespan Gaps Among 183 World Health Organization Member States.183个世界卫生组织成员国的全球健康寿命与寿命差距
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Managing the exponential growth of Mendelian randomization studies.应对孟德尔随机化研究的指数级增长。
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Multi-ancestry meta-analysis of tobacco use disorder identifies 461 potential risk genes and reveals associations with multiple health outcomes.多血统烟草使用障碍的荟萃分析确定了 461 个潜在的风险基因,并揭示了与多种健康结果的关联。
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Biological aging markers in blood and brain tissue indicate age acceleration in alcohol use disorder.血液和脑组织中的生物衰老标志物表明酒精使用障碍患者的年龄加速老化。
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The Impact of Childhood Mental Health and Substance Use on Methylation Aging Into Adulthood.童年心理健康和物质使用对成年后甲基化衰老的影响。
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Multi-ancestry study of the genetics of problematic alcohol use in over 1 million individuals.多血统个体超过 100 万人的问题性饮酒使用的遗传学研究。
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Multi-ancestry genome-wide association study of cannabis use disorder yields insight into disease biology and public health implications.多血统全基因组关联研究大麻使用障碍,深入了解疾病生物学和公共卫生影响。
Nat Genet. 2023 Dec;55(12):2094-2103. doi: 10.1038/s41588-023-01563-z. Epub 2023 Nov 20.
10
Multivariate genome-wide analysis of aging-related traits identifies novel loci and new drug targets for healthy aging.多变量全基因组分析与衰老相关的特征,确定了新的与健康衰老相关的基因座和新的药物靶点。
Nat Aging. 2023 Aug;3(8):1020-1035. doi: 10.1038/s43587-023-00455-5. Epub 2023 Aug 7.