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Schizophrenia-associated variation at ZNF804A correlates with altered experience-dependent dynamics of sleep slow waves and spindles in healthy young adults

Bartsch, Ullrich; Corbin, Laura J.; Hellmich, Charlotte; Taylor, Michelle; Easey, Kayleigh E; Durant, Claire; Marston, Hugh M; Timpson, Nicholas J; Jones, Matthew W.

Authors

Ullrich Bartsch

Laura J. Corbin

Charlotte Hellmich

Michelle Taylor

Kayleigh E Easey

Claire Durant

Hugh M Marston

Nicholas J Timpson

Matthew W. Jones



Abstract

The rs1344706 polymorphism in ZNF804A is robustly associated with schizophrenia and schizophrenia is, in turn, associated with abnormal non-rapid eye movement (NREM) sleep neurophysiology. To examine whether rs1344706 is associated with intermediate neurophysiological traits in the absence of disease, we assessed the relationship between genotype, sleep neurophysiology, and sleep-dependent memory consolidation in healthy participants. We recruited healthy adult males with no history of psychiatric disorder from the Avon Longitudinal Study of Parents and Children (ALSPAC) birth cohort. Participants were homozygous for either the schizophrenia-associated 'A' allele (N = 22) or the alternative 'C' allele (N = 18) at rs1344706. Actigraphy, polysomnography (PSG) and a motor sequence task (MST) were used to characterize daily activity patterns, sleep neurophysiology and sleep-dependent memory consolidation. Average MST learning and sleep-dependent performance improvements were similar across genotype groups, albeit more variable in the AA group. During sleep after learning, CC participants showed increased slow-wave (SW) and spindle amplitudes, plus augmented coupling of SW activity across recording electrodes. SW and spindles in those with the AA genotype were insensitive to learning, whilst SW coherence decreased following MST training. Accordingly, NREM neurophysiology robustly predicted the degree of overnight motor memory consolidation in CC carriers, but not in AA carriers. We describe evidence that rs1344706 polymorphism in ZNF804A is associated with changes in the coordinated neural network activity that supports offline information processing during sleep in a healthy population. These findings highlight the utility of sleep neurophysiology in mapping the impacts of schizophrenia-associated common genetic variants on neural circuit oscillations and function.

Citation

Bartsch, U., Corbin, L. J., Hellmich, C., Taylor, M., Easey, K. E., Durant, C., …Jones, M. W. (2021). Schizophrenia-associated variation at ZNF804A correlates with altered experience-dependent dynamics of sleep slow waves and spindles in healthy young adults. SLEEP, 44(12), https://doi.org/10.1093/sleep/zsab191

Journal Article Type Article
Acceptance Date Jun 6, 2021
Online Publication Date Jul 30, 2021
Publication Date Dec 10, 2021
Deposit Date Sep 23, 2022
Journal Sleep
Print ISSN 0161-8105
Electronic ISSN 1550-9109
Publisher Oxford University Press (OUP)
Peer Reviewed Peer Reviewed
Volume 44
Issue 12
DOI https://doi.org/10.1093/sleep/zsab191
Keywords Physiology (medical); Neurology (clinical), psychosis; schizophrenia; genetics; sleep; slow wave; spindle; motor sequence task; ALSPAC
Public URL https://uwe-repository.worktribe.com/output/10003721
Publisher URL https://academic.oup.com/sleep/article/44/12/zsab191/6331689?login=true