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新西兰纵向队列中重度大麻暴露的全基因组 DNA 甲基化分析。

Genome-wide DNA methylation analysis of heavy cannabis exposure in a New Zealand longitudinal cohort.

机构信息

School of Biological Sciences, University of Canterbury, Christchurch, 8041, New Zealand.

Department of Pathology and Biomedical Science, University of Otago Christchurch, Christchurch, 8011, New Zealand.

出版信息

Transl Psychiatry. 2020 Apr 22;10(1):114. doi: 10.1038/s41398-020-0800-3.

Abstract

Cannabis use is of increasing public health interest globally. Here we examined the effect of heavy cannabis use, with and without tobacco, on genome-wide DNA methylation in a longitudinal birth cohort (Christchurch Health and Development Study, CHDS). A total of 48 heavy cannabis users were selected from the CHDS cohort, on the basis of their adult exposure to cannabis and tobacco, and DNA methylation assessed from whole blood samples, collected at approximately age 28. Methylation in heavy cannabis users was assessed, relative to non-users (n = 48 controls) via the Illumina Infinium® MethylationEPIC BeadChip. We found the most differentially methylated sites in cannabis with tobacco users were in the AHRR and F2RL3 genes, replicating previous studies on the effects of tobacco. Cannabis-only users had no evidence of differential methylation in these genes, or at any other loci at the epigenome-wide significance level (P < 10). However, there were 521 sites differentially methylated at P < 0.001 which were enriched for genes involved in neuronal signalling (glutamatergic synapse and long-term potentiation) and cardiomyopathy. Further, the most differentially methylated loci were associated with genes with reported roles in brain function (e.g. TMEM190, MUC3L, CDC20 and SP9). We conclude that the effects of cannabis use on the mature human blood methylome differ from, and are less pronounced than, the effects of tobacco use, and that larger sample sizes are required to investigate this further.

摘要

大麻使用在全球范围内引起了越来越多的公众健康关注。在这里,我们研究了重度大麻使用者(无论是否同时吸烟草)的全基因组 DNA 甲基化情况,这些人是基于他们成年后的大麻和烟草暴露情况从基督城健康与发展研究(CHDS)队列中选择的。共有 48 名重度大麻使用者入选,他们的 DNA 甲基化情况是从大约 28 岁时采集的全血样本中通过 Illumina Infinium® MethylationEPIC BeadChip 进行评估的。我们通过与非使用者(n=48 名对照)相比,评估了大麻使用者的甲基化情况。我们发现,在同时吸烟草的大麻使用者中,AHRR 和 F2RL3 基因中的甲基化差异最明显,这与之前关于烟草影响的研究结果一致。仅使用大麻的使用者在这些基因或全基因组显著性水平(P<10)的任何其他基因座上均未发现差异甲基化的证据。但是,有 521 个差异甲基化的位点在 P<0.001 时有显著性,这些位点富集了参与神经元信号转导(谷氨酸能突触和长时程增强)和心肌病的基因。此外,差异甲基化最明显的基因座与具有报道的大脑功能相关基因(例如 TMEM190、MUC3L、CDC20 和 SP9)相关。我们得出结论,大麻使用对成熟人类血液甲基组的影响与烟草使用的影响不同,而且也不那么明显,需要更大的样本量来进一步研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a45a/7176736/2f71df517751/41398_2020_800_Fig1_HTML.jpg

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