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. 2018 Dec;42(12):2360-2368.
doi: 10.1111/acer.13905. Epub 2018 Nov 11.

A Whole Methylome Study of Ethanol Exposure in Brain and Blood: An Exploration of the Utility of Peripheral Blood as Proxy Tissue for Brain in Alcohol Methylation Studies

Shaunna L Clark  1   2 , Blair N Costin  3 , Robin F Chan  2 , Alexander W Johnson  1 , Linying Xie  2 , Jessica L Jurmain  3 , Gaurav Kumar  2 , Andrey A Shabalin  2 , Ashutosh K Pandey  4 , Karolina A Aberg  2 , Michael F Miles  3 , Edwin van den Oord  2
Affiliations

A Whole Methylome Study of Ethanol Exposure in Brain and Blood: An Exploration of the Utility of Peripheral Blood as Proxy Tissue for Brain in Alcohol Methylation Studies

Shaunna L Clark et al. Alcohol Clin Exp Res. 2018 Dec.

Abstract

Background: Recent reviews have highlighted the potential use of blood-based methylation biomarkers as diagnostic and prognostic tools of current and future alcohol use and addiction. Due to the substantial overlap that often exists between methylation patterns across different tissues, including blood and brain, blood-based methylation may track methylation changes in brain; however, little work has explored the overlap in alcohol-related methylation in these tissues.

Methods: To study the effects of alcohol on the brain methylome and identify possible biomarkers of these changes in blood, we performed a methylome-wide association study in brain and blood from 40 male DBA/2J mice that received either an acute ethanol (EtOH) or saline intraperitoneal injection. To investigate all 22 million CpGs in the mouse genome, we enriched for the methylated genomic fraction using methyl-CpG binding domain (MBD) protein capture followed by next-generation sequencing (MBD-seq). We performed association tests in blood and brain separately followed by enrichment testing to determine whether there was overlapping alcohol-related methylation in the 2 tissues.

Results: The top result for brain was a CpG located in an intron of Ttc39b (p = 5.65 × 10-08 ), and for blood, the top result was located in Espnl (p = 5.11 × 10-08 ). Analyses implicated pathways involved in inflammation and neuronal differentiation, such as CXCR4, IL-7, and Wnt signaling. Enrichment tests indicated significant overlap among the top results in brain and blood. Pathway analyses of the overlapping genes converge on MAPKinase signaling (p = 5.6 × 10-05 ) which plays a central role in acute and chronic responses to alcohol and glutamate receptor pathways, which can regulate neuroplastic changes underlying addictive behavior.

Conclusions: Overall, we have shown some methylation changes in brain and blood after acute EtOH administration and that the changes in blood partly mirror the changes in brain suggesting the potential for DNA methylation in blood to be biomarkers of alcohol use.

Keywords: Alcohol; Biomarker; Epigenetics; Glutamate; Methylation.

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Figures

Figure 1.
Figure 1.
Enrichment test results for blood and brain MWAS results against genomic features. The x-axis shows the -log10(P-value) for each enrichment test of blood and brain MWAS results against the corresponding genomic features on the y-axis. P-values falling to the right of the vertical dashed line (>1.3 -log10(P-value)) indicate significance at p-value < 0.05.
See this image and copyright information in PMC

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