Association of Unc-51-like Kinase 4 (ULK4) with the reactivity of the extended reward system in response to conditioned stimuli

• Verfasst von: Treutlein, Jens [VerfasserIn]
• Verfasst von: Löhlein, Simone [VerfasserIn]
• Verfasst von: Einenkel, Karolin E. [VerfasserIn]
• Verfasst von: Picotin, Rosanne [VerfasserIn]
• Verfasst von: Diekhof, Esther K. [VerfasserIn]
• Verfasst von: Gruber, Oliver [VerfasserIn]
• Titel: Association of Unc-51-like Kinase 4 (ULK4) with the reactivity of the extended reward system in response to conditioned stimuli
• Verf.angabe: Jens Treutlein, Simone Löhlein, Karolin E. Einenkel, Rosanne Picotin, Esther K. Diekhof, Oliver Gruber
• Jahr: 2024
• Umfang: 8 S.
• Fussnoten: Online veröffentlicht: 26. August 2024 ; Gesehen am 08.10.2024
• Titel Quelle: Enthalten in: The world journal of biological psychiatry
• Ort Quelle: Abingdon : Taylor & Francis Group, 2000
• Jahr Quelle: 2024
• Band/Heft Quelle: 25(2024), 8, Seite 443-450
• ISSN Quelle: 1814-1412
• DOI: doi:10.1080/15622975.2024.2393381
• Datenträger: Online-Ressource
• Sprache: eng
• Sach-SW: biological psychiatry
• Sach-SW: brain imaging
• Sach-SW: extended reward system
• Sach-SW: Genetics
• Sach-SW: ULK4
• K10plus-PPN: 1905066287

Abstract

ULK4 is an established candidate gene for mental disorders and antipsychotic treatment response. We investigated the association of functional genetic variation at the ULK4 locus with the human extended dopaminergic reward system using fMRI during the performance of a well-established reward paradigm. Two hundred and thirty-four patients were included in this study. Association of genetic variation in the ULK4 gene with reward system functioning were determined using the Desire-Reason-Dilemma (DRD) paradigm which allows to assess brain activation in response to conditioned reward stimuli. Variant prioritisation revealed the strongest functional signatures for the ULK4 variant rs17215589, coding for amino acid exchange Ala715Thr. For rs17215589 minor allele carriers, we detected increased activation responses to conditioned reward stimuli in the ventral tegmental area, nucleus accumbens and several cortical brain regions of the extended reward system. Our findings provide further evidence in humans that genetic variation in ULK4 may increase the vulnerability to mental disorders, by modulating the extended reward system function. Future studies are needed to confirm the modulation of the extended reward system by ULK4 and to specify the role of this mechanism in the pathogenesis of psychiatric disorders.