KCNJ6 variants modulate reward-related brain processes and impact executive functions in attention-deficit/hyperactivity disorder

Georg C. Ziegler, Christoph Röser, Tobias Renner, Tim Hahn, Ann Christine Ehlis, Heike Weber, Astrid Dempfle, Susanne Walitza, Christian Jacob, Marcel Romanos, Andreas J. Fallgatter, Andreas Reif, Klaus Peter Lesch

Research output: Contribution to journalArticlepeer-review

12 Citations (Scopus)

Abstract

KCNJ6, encoding a potassium channel subunit, regulates the excitability of dopaminergic neurons and is expressed in attention-deficit/hyperactivity disorder (ADHD)-relevant brain regions. As a potential ADHD risk gene, KCNJ6, therefore, may contribute to the endophenotypic variation of the disorder. The impact of two SNPs, rs7275707 and rs6517442, both located in the transcriptional control region of KCNJ6, on reporter gene expression was explored in cultured cells. The KCNJ6 variants were then tested for association with ADHD and personality traits in a family-based sample (165 affected children) and an adult case–control sample (450 patients, 426 controls). Furthermore, the genotypic influence on performance in an n-back task and a cued continuous performance test (cCPT) was investigated by electroencephalography recordings. Finally, rs6517442 function was assessed by a reward anticipation paradigm using functional magnetic resonance imaging. Different haplotypes of rs7275707 and rs6517442 significantly influenced KCNJ6 gene expression proving their functional relevance on the molecular level. In the family-based children sample rs7275707 was associated with ADHD (p =.038). Moreover, rs7275707 showed association with the personality trait of Reward Dependence (p =.031). In the ADHD group, both rs7275707 and rs6517442 influenced the Go-centroid location in the cCPT and the N200 amplitude in the n-back task. Furthermore, ventral striatal activation was impacted by rs6517442 during reward anticipation. Our data indicate that functional variants of KCNJ6 influence brain activity during reward-related and executive processes supporting the view of a differential, age-dependent modulatory impact of dopamine-related brain processes in ADHD risk.

Original languageEnglish
Pages (from-to)247-257
Number of pages11
JournalAmerican Journal of Medical Genetics, Part B: Neuropsychiatric Genetics
Volume183
Issue number5
DOIs
Publication statusPublished - Jul 1 2020
Externally publishedYes

Bibliographical note

Funding Information:
We are grateful to all patients for their participation in the study. This study was supported by the Deutsche Forschungsgemeinschaft (DFG: CRU 125, CRC TRR 58 A1/A5, CRC1193 Z03), the European Union's Seventh Framework Programme under Grant No. 602805 (Aggressotype), the Horizon 2020 Research and Innovation Programme under Grant No. 728018 (Eat2beNICE), 667302 (CoCA) and 643051 (MiND), Fritz Thyssen Stiftung (No. 10.13.1185), ERA-Net NEURON/RESPOND, No. 01EW1602B, and 5-100 Russian Academic Excellence Project. In addition, this work was supported by the European College of Neuropsychopharmacology (ECNP Network “ADHD across the lifespan”).

Publisher Copyright:
© 2019 Wiley Periodicals, Inc.

ASJC Scopus Subject Areas

  • Genetics(clinical)
  • Psychiatry and Mental health
  • Cellular and Molecular Neuroscience

PubMed: MeSH publication types

  • Journal Article
  • Research Support, Non-U.S. Gov't

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Ziegler, G. C., Röser, C., Renner, T., Hahn, T., Ehlis, A. C., Weber, H., Dempfle, A., Walitza, S., Jacob, C., Romanos, M., Fallgatter, A. J., Reif, A., & Lesch, K. P. (2020). KCNJ6 variants modulate reward-related brain processes and impact executive functions in attention-deficit/hyperactivity disorder. American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics, 183(5), 247-257. https://doi.org/10.1002/ajmg.b.32734