Evidence map›Paper›PMID 39696061›Full record

ArticleBMC pregnancy and childbirth2024

Evaluating causal associations of chronotype with pregnancy and perinatal outcomes and its interactions with insomnia and sleep duration: a mendelian randomization study.

Qian Yang, Maria C Magnus, Fanny Kilpi, Gillian Santorelli, Ana Goncalves Soares, Jane West, Per Magnus, Siri E Håberg, Kate Tilling, Deborah A Lawlor and 2 more

Abstract read
In one paragraph

Article in BMC pregnancy and childbirth, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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2 · The registry

The trial behind it

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

12 authors.

Qian YangMRC Integrative Epidemiology Unit, University of Bristol, Bristol, UK. qian.yang@bristol.ac.uk.ORCID http://orcid.org/0000-0001-8778-4132
Maria C MagnusMRC Integrative Epidemiology Unit, University of Bristol, Bristol, UK.ORCID http://orcid.org/0000-0002-0568-3774
Fanny KilpiMRC Integrative Epidemiology Unit, University of Bristol, Bristol, UK.ORCID http://orcid.org/0000-0002-3551-2829
Gillian SantorelliMRC Integrative Epidemiology Unit, University of Bristol, Bristol, UK.ORCID http://orcid.org/0000-0003-0427-1783
Ana Goncalves SoaresMRC Integrative Epidemiology Unit, University of Bristol, Bristol, UK.ORCID http://orcid.org/0000-0003-2763-4647
Jane WestBradford Institute for Health Research, Bradford Teaching Hospitals NHS Foundation Trust, Bradford, UK.ORCID http://orcid.org/0000-0002-5770-8363
Per MagnusCentre for Fertility and Health, Norwegian Institute of Public Health, Oslo, Norway.
Siri E HåbergCentre for Fertility and Health, Norwegian Institute of Public Health, Oslo, Norway.ORCID http://orcid.org/0000-0002-2199-5225
Kate Tilling *MRC Integrative Epidemiology Unit, University of Bristol, Bristol, UK.ORCID http://orcid.org/0000-0002-1010-8926
Deborah A Lawlor *MRC Integrative Epidemiology Unit, University of Bristol, Bristol, UK.ORCID http://orcid.org/0000-0002-6793-2262
M Carolina Borges *MRC Integrative Epidemiology Unit, University of Bristol, Bristol, UK.ORCID http://orcid.org/0000-0001-7785-4547
Eleanor Sanderson *MRC Integrative Epidemiology Unit, University of Bristol, Bristol, UK.ORCID http://orcid.org/0000-0001-5188-5775

Funding

British Heart Foundation CH/F/20/90003China Scholarship Council CSC201808060273European Research Council 101071773H2020 European Research Council 847684Medical Research Council MC_UU_00032/01Medical Research Council MC_UU_00032/02Medical Research Council MC_UU_00032/05Medical Research Council MC_UU_00032/1Medical Research Council MC_UU_00032/2Medical Research Council MC_UU_00032/5Medical Research Council MR/P014054/1NIHR Bristol Biomedical Research Centre NF-0616-10102Norges Forskningsråd 262700
6 · The paper itself

Abstract

backgroundObservational studies suggested chronotype was associated with pregnancy and perinatal outcomes. Whether these associations are causal is unclear. Our aims are to use Mendelian randomization (MR) to explore (1) associations of evening preference with stillbirth, miscarriage, gestational diabetes, hypertensive disorders of pregnancy, perinatal depression, preterm birth and offspring birthweight; and (2) differences in associations of insomnia and sleep duration with those outcomes between chronotype preferences.

methodsWe conducted two-sample MR using 105 genetic variants reported in a genome-wide association study (N = 248,100) to instrument for lifelong predisposition to evening- versus morning-preference. We generated variant-outcome associations in European ancestry women from UK Biobank (UKB, N = 176,897), Avon Longitudinal Study of Parents and Children (ALSPAC, N = 6826), Born in Bradford (BiB, N = 2940) and the Norwegian Mother, Father and Child Cohort Study (MoBa, N = 57,430), and extracted equivalent associations from FinnGen (N = 190,879). We used inverse variance weighted (IVW) as main analysis, with weighted median and MR-Egger as sensitivity analyses. Relying on the individual participant data from UKB, ALSPAC, BiB and MoBa, we also conducted IVW analyses of insomnia and sleep duration on the pregnancy and perinatal outcomes, stratified by genetically predicted chronotypes.

resultsIn IVW and sensitivity analyses, we did not find robust evidence of associations of chronotype with the outcomes. Insomnia was associated with a higher risk of preterm birth among evening preference women (odds ratio 1.61, 95% confidence interval: 1.17, 2.21), but not among morning preference women (odds ratio 0.87, 95% confidence interval: 0.64, 1.18), with an interaction P-value = 0.01. There was no evidence of interactions between insomnia and chronotype on other outcomes, or between sleep duration and chronotype on any outcomes.

conclusionsThis study raises the possibility of a higher risk of preterm birth among women with insomnia who also have an evening preference. Our findings warrant replications due to imprecise estimates.

Indexed as

Mendelian Randomization AnalysisPregnancy OutcomeSleepSleep Initiation and Maintenance DisordersAdultChronotypeCircadian RhythmFemaleGenome-Wide Association StudyHumansLongitudinal StudiesPregnancyPregnancy ComplicationsPremature BirthSleep DurationUnited KingdomChronotypeMendelian randomizationPregnancy and perinatal outcomesSleep

Identifiers

PMID39696061
PMCPMC11654309

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LicenceCC BY
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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.