甲基化
双相情感障碍
表观遗传学
CpG站点
内科学
医学
候选基因
肿瘤科
DNA甲基化
基因
生物信息学
遗传学
生物
基因表达
锂(药物)
作者
Zhang Hs,Ke Xy,Hu Ll,J Wang,Gao Ls,Jiansheng Xie
出处
期刊:PubMed
日期:2018-03-01
卷期号:22 (5): 1421-1425
被引量:7
标识
DOI:10.26355/eurrev_201803_14489
摘要
We aimed to study changes and possible roles of epigenetic modification of candidate genes in the pathogenesis of bipolar disorder, and provide the basis for clinical diagnosis and analysis.A total of 150 patients with bipolar disorder were enrolled in this study from January 2014 to June 2015; also, 50 healthy subjects were enrolled as control group. The patients were followed up for 18 months and followed up once every 3 months to review the methylation status. The methylation status was examined before and after treatment, and the patients were followed up every 3 months after treatment, and the follow-up period was 18 months.Compared with the healthy control group, there were 2075 CpG island aberrant methylation points in patients with bipolar disorder, which can be divided into 24 categories. Log-Ratio > 0.5 was used as the positive criteria, and COMT and PPIEL were identified as the genes associated with bipolar disorder. Compared with the control group, the levels of COMT and PPIEL gene methylation in the observation group were significantly higher (p < 0.05). There was no significant difference in the methylation level of COMT and PPIEL gene between the two groups (p > 0.05) after 12 months of treatment.The methylation level of COMT and PPIEL gene is closely related to bipolar disorder.
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