Correlation Engine 2.0
Clear Search sequence regions


  • d (3)
  • diagnosis (3)
  • GRIN2A (4)
  • GRIN2B (4)
  • humans (1)
  • impairment (1)
  • methyl (3)
  • NMDA receptor (1)
  • nr2b nmda receptor (1)
  • patients (3)
  • reaction time (1)
  • receptors (3)
  • Sizes of these terms reflect their relevance to your search.

    Objective: To examine the association between variants of N-methyl-D-aspartate (NMDA) receptor subunit-encoding genes (GRIN2A and GRIN2B) and continuous performance test (CPT) variables in ADHD and healthy controls. Method: In all, 253 ADHD patients and 98 controls were recruited. The diagnosis, genotype, and diagnosis-genotype interaction effects for the CPT variables were examined. Results: Significant diagnosis effects were detected for all CPT variables. There were significant genotype and interaction effects on response time variability (RTV) by the GRIN2B variant. The C/C subgroup had higher RTV than the C/T + T/T subgroup in ADHD, but not in controls. There were significant genotype effects on omission errors by the GRIN2A variant. The G/G subgroup had more omission errors than the G/A + A/A subgroup in ADHD patients, but not in controls. Conclusion: These results suggest that the genetic variants of GRIN2B and GRIN2A confer an increased susceptibility to attentional impairment in ADHD patients.

    Citation

    Johanna Inhyang Kim, Jae-Won Kim, Subin Park, Soon-Beom Hong, Dong Soo Lee, Sun Ha Paek, Doug Hyun Han, Jae Hoon Cheong, Bung-Nyun Kim. The GRIN2B and GRIN2A Gene Variants Are Associated With Continuous Performance Test Variables in ADHD. Journal of attention disorders. 2020 Sep;24(11):1538-1546

    Expand section icon Mesh Tags

    Expand section icon Substances


    PMID: 27199241

    View Full Text