Evidence map›Paper›PMID 39667926›Full record

ArticleBMJ mental health2024

Genetic variation in circadian regulator gene

Hamza Daudali, Jana Anderson, Mark E S Bailey, Alexander Fradera, Claire L Niedzwiedz, Donald Lyall, Laura M M Lyall, Rona J Strawbridge

Abstract read
In one paragraph

Article in BMJ mental health, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
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

3 citing papers in PubMed.

  1. Social Rhythms, Depressive Symptoms, and Quality of Life: An Unbreakable Bond in an Older Adult Sample.International journal of environmental research and public health · 2026
    Observational
  2. Review
  3. Circadian rhythms and mental health.BMJ mental health · 2025
    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

8 authors.

Hamza DaudaliUniversity of Glasgow, Glasgow, UK.
Jana AndersonUniversity of Glasgow, Glasgow, UK.
Mark E S BaileyUniversity of Glasgow, Glasgow, UK.
Alexander FraderaUniversity of Glasgow, Glasgow, UK.
Claire L NiedzwiedzUniversity of Glasgow, Glasgow, UK.ORCID 0000-0001-6133-4168
Donald LyallUniversity of Glasgow, Glasgow, UK.ORCID 0000-0003-3850-1487
Laura M M LyallUniversity of Glasgow, Glasgow, UK.
Rona J StrawbridgeUniversity of Glasgow, Glasgow, UK rona.strawbridge@glasgow.ac.uk.ORCID 0000-0001-8506-3585

Funding

Medical Research Council MR/S003061/1Wellcome Trust
6 · The paper itself

Abstract

backgroundThe link between cardiometabolic disease and mental illness has been well established but remains incompletely explained. One hypothesis suggests that circadian rhythm dysregulation links cardiometabolic disease and mental illnesses.

objectiveWe investigated the

methodsGenetic and phenotypic data from UK Biobank (~500 000 participants) of White British, African-Caribbean, South Asian, white European and Multiple ancestries were used. Regression analyses using Plink 1.09 was used to identify significant associations, with Bonferroni multiple testing correction. Multiple ancestry meta-analyses using METAL software was used to investigate trans-ancestry consistency in genetic effects.

findingsWe identified associations for body mass index, anhedonia, diastolic and systolic blood pressure, waist-hip ratio, major depressive disorder, neuroticism and risk-taking. Meta-analyses indicated that there are ancestry-wide and ancestry-specific effects on cardiometabolic, mental illness and related traits.

conclusionsOur results suggest that the associations for mental illness (and related traits) and those for cardiometabolic traits are distinct rather than shared and that these associations were consistent across ancestry groups. CLINICAL IMPLICATIONS: Further investigation into the tissue-specific roles of

Indexed as

ARNTL Transcription FactorsBiological Specimen BanksAdultAgedBlood PressureBody Mass IndexCardiovascular DiseasesFemaleGenetic Predisposition to DiseaseGenetic VariationHumansMajor Depressive DisorderMaleMental DisordersMiddle AgedNeuroticismARNTL Transcription FactorsBMAL1 protein, humanCross-Sectional StudiesData Interpretation, StatisticalPSYCHIATRY

Identifiers

PMID39667926
PMCPMC11647332

What OpenQuestion holds

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Registered trials

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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.