Frontiers in Psychiatry (Mar 2018)

Circulating MicroRNA Expression Levels Associated With Internet Gaming Disorder

  • Minho Lee,
  • Hyeyoung Cho,
  • Hyeyoung Cho,
  • Seung Hyun Jung,
  • Seung Hyun Jung,
  • Seon-Hee Yim,
  • Sung-Min Cho,
  • Sung-Min Cho,
  • Ji-Won Chun,
  • Soo-Hyun Paik,
  • Yae Eun Park,
  • Yae Eun Park,
  • Dong Huey Cheon,
  • Dong Huey Cheon,
  • Ji Eun Lee,
  • Jung-Seok Choi,
  • Dai-Jin Kim,
  • Yeun-Jun Chung,
  • Yeun-Jun Chung,
  • Yeun-Jun Chung

DOI
https://doi.org/10.3389/fpsyt.2018.00081
Journal volume & issue
Vol. 9

Abstract

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BackgroundAddictive 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.MethodsTo 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).ResultsThrough 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.ConclusionWe 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.

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