Evidence map›Paper›PMID 30120083›Full record

ArticleEBioMedicine2018

Genome-Wide Association Study of Circadian Rhythmicity in 71,500 UK Biobank Participants and Polygenic Association with Mood Instability.

Amy Ferguson, Laura M Lyall, Joey Ward, Rona J Strawbridge, Breda Cullen, Nicholas Graham, Claire L Niedzwiedz, Keira J A Johnston, Daniel MacKay, Stephany M Biello and 8 more

Registry-linked trialOpen access · goldAbstract read
In one paragraph

Article in EBioMedicine, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT05153941 (DNS Cohort Study Aimed at Understanding the Pathophysiology of AD and AD Related Disorders), which is not on this map. Cited by 40 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed, 1 pooled it
3.5field-weighted citation impact, top 6% 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.

NCT05153941 active not recruitingnot on this mapstarted 2022, after this paper: background citation

DNS Cohort Study Aimed at Understanding the Pathophysiology of AD and AD Related Disorders (ADRD)

TypeobservationalSponsorAltoidaRan2022 to 2030Enrolled3,500ConditionsAlzheimer's Disease, Mild Cognitive Impairment
3 · Its place in the literature

Who cites it

40 citing papers in PubMed, 1 synthesis or guideline pooled it, 72 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Trial
  4. Review
  5. Article
  6. Review
  7. Review
  8. Article
  9. Article
  10. Article
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  12. [Association of Rest-Activity Rhythm With the Risk of Rheumatoid Arthritis and Effect Modification by Genetic Susceptibility].Sichuan da xue xue bao. Yi xue ban = Journal of Sichuan University. Medical science edition · 2025
    Article
  13. Article
  14. Article
  15. Relationship between Polygenic Risk Score and the Hypnotics in Bipolar I Disorder.Clinical psychopharmacology and neuroscience : the official scientific journal of the Korean College of Neuropsychopharmacology · 2024
    Article
  16. Review
  17. Article
  18. The sleep-circadian interface: A window into mental disorders.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Review
  19. Review
  20. 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

18 authors at 4 institutions in 3 countries.

Amy FergusonInstitute of Health & Wellbeing, University of Glasgow, Scotland, UK. Electronic address: a.ferguson.3@research.gla.ac.uk.
Laura M LyallInstitute of Health & Wellbeing, University of Glasgow, Scotland, UK.
Joey WardInstitute of Health & Wellbeing, University of Glasgow, Scotland, UK.
Rona J StrawbridgeInstitute of Health & Wellbeing, University of Glasgow, Scotland, UK; Department of Medicine Solna, Karolinska Institute, Stockholm, Sweden.
Breda CullenInstitute of Health & Wellbeing, University of Glasgow, Scotland, UK.
Nicholas GrahamInstitute of Health & Wellbeing, University of Glasgow, Scotland, UK.
Claire L NiedzwiedzInstitute of Health & Wellbeing, University of Glasgow, Scotland, UK.
Keira J A JohnstonInstitute of Health & Wellbeing, University of Glasgow, Scotland, UK.
Daniel MacKayInstitute of Health & Wellbeing, University of Glasgow, Scotland, UK.
Stephany M BielloInstitute of Neuroscience and Psychology, University of Glasgow, Scotland, UK.
Jill P PellInstitute of Health & Wellbeing, University of Glasgow, Scotland, UK.
Jonathan CavanaghInstitute of Health & Wellbeing, University of Glasgow, Scotland, UK.
Andrew M McIntoshCentre for Cognitive Ageing and Cognitive Epidemiology, University of Edinburgh, Scotland, UK.
Aiden DohertyBig Data Institute, Nuffield Department of Population Health, BHF Centre of Research Excellence, University of Oxford, Oxford, UK; Institute of Biomedical Engineering, Department of Engineering Science, University of Oxford, Oxford, UK.
Mark E S BaileySchool of Life Sciences, College of Medical, Veterinary and Life Sciences, University of Glasgow, Scotland, UK.
Donald M LyallInstitute of Health & Wellbeing, University of Glasgow, Scotland, UK.
Cathy A WyseDepartment of Molecular and Cellular Therapeutics, Irish Centre for Vascular Biology, Royal College of Surgeons in Ireland (RCSI), Dublin, Ireland.
Daniel J SmithInstitute of Health & Wellbeing, University of Glasgow, Scotland, UK. Electronic address: Daniel.Smith@glasgow.ac.uk.
University of Glasgow · GBRoyal College of Surgeons in Ireland · IEUniversity of Edinburgh · GBUniversity of Oxford · GB

Funding

Medical Research Council MC_PC_17228Medical Research Council MC_QA137853Medical Research Council MR/K026992/1Medical Research Council MR/R024774/1Medical Research Council MR/S003061/1Wellcome Trust
6 · The paper itself

Abstract

backgroundCircadian rhythms are fundamental to health and are particularly important for mental wellbeing. Disrupted rhythms of rest and activity are recognised as risk factors for major depressive disorder and bipolar disorder.

methodsWe conducted a genome-wide association study (GWAS) of low relative amplitude (RA), an objective measure of rest-activity cycles derived from the accelerometer data of 71,500 UK Biobank participants. Polygenic risk scores (PRS) for low RA were used to investigate potential associations with psychiatric phenotypes. OUTCOMES: Two independent genetic loci were associated with low RA, within genomic regions for Neurofascin (NFASC) and Solute Carrier Family 25 Member 17 (SLC25A17). A secondary GWAS of RA as a continuous measure identified a locus within Meis Homeobox 1 (MEIS1). There were no significant genetic correlations between low RA and any of the psychiatric phenotypes assessed. However, PRS for low RA was significantly associated with mood instability across multiple PRS thresholds (at PRS threshold 0·05: OR = 1·02, 95% CI = 1·01-1·02, p = 9·6 × 10

interpretationOverall, our findings contribute new knowledge on the complex genetic architecture of circadian rhythmicity and suggest a putative biological link between disrupted circadian function and mood disorder phenotypes, particularly mood instability, but also major depressive disorder and neuroticism.

fundingMedical Research Council (MR/K501335/1).

Indexed as

Biological Specimen BanksGenome-Wide Association StudyAdultAgedCircadian RhythmHumansMental DisordersMiddle AgedMood DisordersMultifactorial InheritancePhenotypePolymorphism, Single NucleotideQuantitative Trait LociCircadian rhythmicityGwasMood instabilityPolygenic risk scoreRelative amplitude

Identifiers

PMID30120083
PMCPMC6154782
OpenAlexW2809445594

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

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.