Department of Child and Adolescent Psychiatry, NYU Langone Medical Center, New York, New York.
Center for Behavioral Science Research, Department of Health Policy & Health Services Research, Boston University Henry M Goldman School of Dental Medicine, Boston, Massachusetts.
Alcohol Clin Exp Res. 2019 Apr;43(4):628-639. doi: 10.1111/acer.13971. Epub 2019 Mar 4.
Alcohol use disorder (AUD) is a wide-spread, heritable brain disease, but few studies have linked genetic variants or epigenetic factors to brain structures related to AUD in humans, due to many factors including the high-dimensional nature of imaging and genomic data.
To provide potential insights into the links among epigenetic regulation, brain structure, and AUD, we have performed an integrative analysis of brain structural imaging and blood DNA methylome data from 52 AUD and 58 healthy control (HC) subjects collected in the Nathan Kline Institute-Rockland Sample.
We first found that AUD subjects had significantly larger insular surface area than HC in both left and right hemispheres. We then found that 7,827 DNA methylation probes on the HumanMethylation450K BeadChip had significant correlations with the right insular surface area (false discovery rate [FDR] < 0.05). Furthermore, we showed that 44 of the insular surface area-correlated methylation probes were also strongly correlated with AUD status (FDR < 0.05). These AUD-correlated probes are annotated to 36 protein-coding genes, with 16 genes (44%) having been reported by others to be related to AUD or alcohol response, including TAS2R16 and PER2. The remaining 20 genes, in particular ARHGAP22, might represent novel genes involved in AUD or responsive to alcohol.
We have identified 36 insular surface area- and AUD-correlated protein-coding genes that are either known to be AUD- or alcohol-related or not yet reported by prior studies. Therefore, our study suggests that the brain imaging-guided epigenetic analysis has a potential of identifying possible epigenetic mechanisms involved in AUD.
酒精使用障碍(AUD)是一种广泛存在的遗传性脑部疾病,但由于成像和基因组数据的高维性质等诸多因素,很少有研究将遗传变异或表观遗传因素与人类 AUD 相关的大脑结构联系起来。
为了深入了解表观遗传调控、大脑结构和 AUD 之间的联系,我们对来自 Nathan Kline Institute-Rockland Sample 的 52 名 AUD 患者和 58 名健康对照(HC)受试者的大脑结构成像和血液 DNA 甲基化组数据进行了综合分析。
我们首先发现,AUD 受试者的左右半球岛叶表面积均显著大于 HC 受试者。然后我们发现,在 HumanMethylation450K BeadChip 上的 7827 个 DNA 甲基化探针与右侧岛叶表面积显著相关(错误发现率[FDR]<0.05)。此外,我们还发现,44 个与岛叶表面积相关的甲基化探针与 AUD 状态也呈强烈相关(FDR<0.05)。这些与 AUD 相关的探针注释到 36 个蛋白编码基因,其中 16 个基因(44%)已被报道与 AUD 或酒精反应有关,包括 TAS2R16 和 PER2。其余 20 个基因,特别是 ARHGAP22,可能代表与 AUD 相关或对酒精有反应的新基因。
我们已经确定了 36 个与岛叶表面积和 AUD 相关的蛋白编码基因,这些基因要么已知与 AUD 或酒精有关,要么是之前的研究尚未报道的。因此,我们的研究表明,大脑成像指导的表观遗传分析有可能确定 AUD 中涉及的潜在表观遗传机制。