Center for Omics Discovery and Epidemiology, RTI International, Research Triangle Park, North Carolina, USA.
Epidemiology Branch, National Institute of Environmental Health Sciences, Research Triangle Park, North Carolina, USA.
Am J Med Genet B Neuropsychiatr Genet. 2021 Apr;186(3):173-182. doi: 10.1002/ajmg.b.32813. Epub 2020 Aug 17.
Cannabis use is highly prevalent and is associated with adverse and beneficial effects. To better understand the full spectrum of health consequences, biomarkers that accurately classify cannabis use are needed. DNA methylation (DNAm) is an excellent candidate, yet no blood-based epigenome-wide association studies (EWAS) in humans exist. We conducted an EWAS of lifetime cannabis use (ever vs. never) using blood-based DNAm data from a case-cohort study within Sister Study, a prospective cohort of women at risk of developing breast cancer (Discovery N = 1,730 [855 ever users]; Replication N = 853 [392 ever users]). We identified and replicated an association with lifetime cannabis use at cg15973234 (CEMIP): combined p = 3.3 × 10 . We found no overlap between published blood-based cis-meQTLs of cg15973234 and reported lifetime cannabis use-associated single nucleotide polymorphism (SNPs; p < .05), suggesting that the observed DNAm difference was driven by cannabis exposure. We also developed a multi-CpG classifier of lifetime cannabis use using penalized regression of top EWAS CpGs. The resulting 50-CpG classifier produced an area under the curve (AUC) = 0.74 (95% CI [0.72, 0.76], p = 2.00 × 10 ) in the discovery sample and AUC = 0.54 ([0.51, 0.57], p = 2.87 × 10 ) in the replication sample. Our EWAS findings provide evidence that blood-based DNAm is associated with lifetime cannabis use.
大麻使用非常普遍,与不良和有益的影响有关。为了更好地了解健康后果的全貌,需要能够准确分类大麻使用的生物标志物。DNA 甲基化(DNAm)是一个很好的候选者,但目前在人类中还没有基于血液的全基因组关联研究(EWAS)。我们使用 Sister 研究中的病例-队列研究中的基于血液的 DNAm 数据进行了一项终生大麻使用(曾经与从不)的 EWAS,该研究是乳腺癌风险女性的前瞻性队列(发现队列 N=1730[855 名曾经使用者];复制队列 N=853[392 名曾经使用者])。我们鉴定并复制了与 cg15973234 处终生大麻使用的关联(CEMIP):合并 p=3.3×10-8。我们在 cg15973234 处发现的已发表的基于血液的 cis-meQTL 与报告的终生大麻使用相关的单核苷酸多态性(SNP)之间没有重叠(p<.05),这表明观察到的 DNAm 差异是由大麻暴露引起的。我们还使用顶级 EWAS CpG 的惩罚回归开发了终生大麻使用的多-CpG 分类器。由此产生的 50-CpG 分类器在发现样本中的曲线下面积(AUC)为 0.74(95%CI [0.72, 0.76],p=2.00×10-8),在复制样本中的 AUC 为 0.54([0.51, 0.57],p=2.87×10-8)。我们的 EWAS 研究结果提供了证据,证明基于血液的 DNAm 与终生大麻使用有关。