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年轻人中使用大麻与基于 DNA 甲基化的生物年龄。

Marijuana use and DNA methylation-based biological age in young adults.

机构信息

Department of Preventive Medicine, Northwestern University Feinberg School of Medicine, 680 N. Lake Shore Drive, Suite 1400, Chicago, IL, 60611, USA.

Division of Biostatistics, Washington University, St. Louis, MO, USA.

出版信息

Clin Epigenetics. 2022 Oct 26;14(1):134. doi: 10.1186/s13148-022-01359-8.

Abstract

BACKGROUND

Marijuana is the third most commonly used drug in the USA and efforts to legalize it for medical and recreational use are growing. Despite the increase in use, marijuana's effect on aging remains understudied and understanding the effects of marijuana on molecular aging may provide novel insights into the role of marijuana in the aging process. We therefore sought to investigate the association between cumulative and recent use of marijuana with epigenetic age acceleration (EAA) as estimated from blood DNA methylation.

RESULTS

A random subset of participants from The Coronary Artery Risk Development in Young Adults (CARDIA) Study with available whole blood at examination years (Y) 15 and Y20 underwent epigenomic profiling. Four EAA estimates (intrinsic epigenetic age acceleration, extrinsic epigenetic age acceleration, PhenoAge acceleration, and GrimAge acceleration) were calculated from DNA methylation levels measured at Y15 and Y20. Ever use and cumulative marijuana-years were calculated from the baseline visit to Y15 and Y20, and recent marijuana use (both any and number of days of use in the last 30 days) were calculated at Y15 and Y20. Ever use of marijuana and each additional marijuana-year were associated with a 6-month (P < 0.001) and a 2.5-month (P < 0.001) higher average in GrimAge acceleration (GAA) using generalized estimating equations, respectively. Recent use and each additional day of recent use were associated with a 20-month (P < 0.001) and a 1-month (P < 0.001) higher GAA, respectively. A statistical interaction between marijuana-years and alcohol consumption on GAA was observed (P = 0.011), with nondrinkers exhibiting a higher GAA (β = 0.21 [95% CI 0.05, 0.36], P = 0.008) compared to heavy drinkers (β = 0.05 [95% CI - 0.09, 0.18], P = 0.500) per each additional marijuana-year. No associations were observed for the remaining EAA estimates.

CONCLUSIONS

These findings suggest cumulative and recent marijuana use are associated with age-related epigenetic changes that are related to lifespan. These observed associations may be modified by alcohol consumption. Given the increase in use and legalization, these findings provide novel insight on the effect of marijuana use on the aging process as captured through blood DNA methylation.

摘要

背景

大麻是美国使用第三多的毒品,将其合法化用于医疗和娱乐用途的努力正在增加。尽管使用量增加,但大麻对衰老的影响仍未得到充分研究,了解大麻对分子衰老的影响可能为大麻在衰老过程中的作用提供新的见解。因此,我们试图调查从血液 DNA 甲基化中估计的累积和最近使用大麻与表观遗传年龄加速 (EAA) 之间的关联。

结果

一项来自“冠状动脉风险发展在年轻人”(CARDIA)研究的随机参与者子集,在 Y15 和 Y20 年的检查时有可用的全血,进行了表观基因组分析。从 Y15 和 Y20 测量的 DNA 甲基化水平计算了四个 EAA 估计值(内在表观遗传年龄加速、外在表观遗传年龄加速、PhenoAge 加速和 GrimAge 加速)。从基线访视到 Y15 和 Y20 计算了大麻的累积使用年限和累积大麻年数,在 Y15 和 Y20 计算了最近的大麻使用(包括过去 30 天内使用的任何天数和使用天数)。在广义估计方程中,大麻的既往使用和每增加一年大麻使用与平均 GrimAge 加速(GAA)增加 6 个月(P < 0.001)和 2.5 个月(P < 0.001)分别相关。最近使用和最近每天使用的天数分别与 GAA 增加 20 个月(P < 0.001)和 1 个月(P < 0.001)相关。在 GAA 上观察到大麻年数和酒精消耗之间的统计学相互作用(P = 0.011),与非饮酒者相比,重度饮酒者每增加一年大麻使用,GAA 增加更高(β = 0.21 [95%CI 0.05, 0.36],P = 0.008)。与重度饮酒者(β = 0.05 [95%CI -0.09, 0.18],P = 0.500)相比,非饮酒者的 GAA 更高(β = 0.21 [95%CI 0.05, 0.36],P = 0.008)。没有观察到其余 EAA 估计值的关联。

结论

这些发现表明,累积和最近使用大麻与与寿命相关的表观遗传变化有关。这些观察到的关联可能受到酒精消耗的影响。鉴于使用量的增加和合法化,这些发现为通过血液 DNA 甲基化评估大麻使用对衰老过程的影响提供了新的见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1e85/9609285/3b391f88cfec/13148_2022_1359_Fig1_HTML.jpg

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