Lee Minho, Cho Hyeyoung, Jung Seung Hyun, Yim Seon-Hee, Cho Sung-Min, Chun Ji-Won, Paik Soo-Hyun, Park Yae Eun, Cheon Dong Huey, Lee Ji Eun, Choi Jung-Seok, Kim Dai-Jin, Chung Yeun-Jun
Catholic Precision Medicine Research Center, College of Medicine, The Catholic University of Korea, Seoul, South Korea.
Integrated Research Center for Genome Polymorphism, College of Medicine, The Catholic University of Korea, Seoul, South Korea.
Front Psychiatry. 2018 Mar 12;9:81. doi: 10.3389/fpsyt.2018.00081. eCollection 2018.
Addictive use of the Internet and online games is a potential psychiatric disorder termed Internet gaming disorder (IGD). Altered microRNA (miRNA) expression profiles have been reported in blood and brain tissue of patients with certain psychiatric disorders and suggested as biomarkers. However, there have been no reports on blood miRNA profiles in IGD.
To discover IGD-associated miRNAs, we analyzed the miRNA expression profiles of 51 samples (25 IGD and 26 controls) using the TaqMan Low Density miRNA Array. For validation, we performed quantitative reverse transcription PCR with 36 independent samples (20 IGD and 16 controls).
Through discovery and independent validation, we identified three miRNAs (hsa-miR-200c-3p, hsa-miR-26b-5p, hsa-miR-652-3p) that were significantly downregulated in the IGD group. Individuals with all three miRNA alterations had a much higher risk of IGD than those with no alteration [odds ratio (OR) 22, 95% CI 2.29-211.11], and the ORs increased dose dependently with number of altered miRNAs. The predicted target genes of the three miRNAs were associated with neural pathways. We explored the protein expression of the three downstream target genes by western blot and confirmed that expression of GABRB2 and DPYSL2 was significantly higher in the IGD group.
We observed that expressions of hsa-miR-200c-3p, hsa-miR-26b-5p, and hsa-miR-652-3p were downregulated in the IGD patients. Our results will be helpful to understand the pathophysiology of IGD.
互联网和网络游戏成瘾是一种潜在的精神障碍,称为网络游戏障碍(IGD)。在某些精神障碍患者的血液和脑组织中,已报道了微小RNA(miRNA)表达谱的改变,并被认为是生物标志物。然而,关于IGD患者血液miRNA谱的报道尚无。
为了发现与IGD相关的miRNA,我们使用TaqMan低密度miRNA阵列分析了51个样本(25例IGD和26例对照)的miRNA表达谱。为了进行验证,我们对36个独立样本(20例IGD和16例对照)进行了定量逆转录PCR。
通过发现和独立验证,我们鉴定出三种miRNA(hsa-miR-200c-3p、hsa-miR-26b-5p、hsa-miR-652-3p)在IGD组中显著下调。与无改变的个体相比,三种miRNA均改变的个体患IGD的风险要高得多[比值比(OR)22,95%置信区间2.29 - 211.11],并且OR随改变的miRNA数量呈剂量依赖性增加。这三种miRNA的预测靶基因与神经通路相关。我们通过蛋白质印迹法探索了三种下游靶基因的蛋白质表达,并证实GABRB2和DPYSL2的表达在IGD组中显著更高。
我们观察到IGD患者中hsa-miR-200c-3p、hsa-miR-26b-5p和hsa-miR-652-3p的表达下调。我们的结果将有助于理解IGD的病理生理学。