Evidence map›Paper›PMID 34329479›Full record

ArticleSleep2021

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

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

Open access · hybridAbstract read
In one paragraph

Article in Sleep, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed, 1 pooled it
0.1field-weighted citation impact, top 58% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed, 1 synthesis or guideline pooled it, 3 citations in OpenAlex.

  1. Pooled it
  2. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors at 3 institutions in 2 countries.

Ullrich BartschSchool of Physiology, Pharmacology & Neuroscience, University of Bristol, Bristol, UK.ORCID 0000-0002-2213-8989
Laura J CorbinMRC Integrative Epidemiology Unit at University of Bristol, Bristol, UK.ORCID 0000-0002-4032-9500
Charlotte HellmichSchool of Physiology, Pharmacology & Neuroscience, University of Bristol, Bristol, UK.
Michelle TaylorMRC Integrative Epidemiology Unit at University of Bristol, Bristol, UK.
Kayleigh E EaseyMRC Integrative Epidemiology Unit at University of Bristol, Bristol, UK.
Claire DurantClinical Research and Imaging Centre (CRIC), University of Bristol, Bristol, UK.
Hugh M MarstonTranslational Neuroscience, Eli Lilly & Co Ltd UK, Erl Wood Manor, Windlesham, UK.
Nicholas J TimpsonMRC Integrative Epidemiology Unit at University of Bristol, Bristol, UK.
Matthew W JonesSchool of Physiology, Pharmacology & Neuroscience, University of Bristol, Bristol, UK.ORCID 0000-0001-5396-3108
University of Bristol · GBBoehringer Ingelheim (Germany) · DEUniversity of Surrey · GB

Funding

Cancer Research UK C18281/A29019Medical Research Council G0701503/85179Medical Research Council G1002064Medical Research Council MC_PC_15018Medical Research Council MC_UU_00011/1Medical Research Council MC_UU_12013/3Wellcome Trust 076467/Z/05/ZWellcome Trust 202802/Z/16/ZWellcome Trust 202810/Z/16/ZWellcome Trust 217065/Z/19/Z
6 · The paper itself

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.

Indexed as

Memory ConsolidationSchizophreniaChildHumansKruppel-Like Transcription FactorsLongitudinal StudiesMalePolysomnographySleepYoung AdultKruppel-Like Transcription FactorsZNF804A protein, humanALSPACgeneticsmotor sequence taskpsychosisschizophreniasleepslow wavespindle

Identifiers

PMID34329479
PMCPMC8664578
OpenAlexW3186326204

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.