Evidence mapPaperPMID 38084713Full record

ArticleJournal of the American Heart Association2023

Causal Association Between Subtypes of Excessive Daytime Sleepiness and Risk of Cardiovascular Diseases.

Matthew O Goodman, Hassan S Dashti, Jacqueline M Lane, Daniel P Windred, Angus Burns, Samuel E Jones, Tamar Sofer, Shaun M Purcell, Xiaofeng Zhu, Hanna M Ollila and 10 more

Open access · goldAbstract read
In one paragraph

Article in Journal of the American Heart Association, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed, 2 pooled it
5.1field-weighted citation impact, top 4% 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

10 citing papers in PubMed, 2 syntheses or guidelines pooled it, 20 citations in OpenAlex.

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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

20 authors at 8 institutions in 7 countries.

Matthew O GoodmanDivision of Sleep and Circadian Disorders Brigham and Women's Hospital Boston MA.ORCID 0000-0002-3982-7940
Hassan S DashtiBroad Institute Cambridge MA.ORCID 0000-0002-1650-679X
Jacqueline M LaneDivision of Sleep and Circadian Disorders Brigham and Women's Hospital Boston MA.ORCID 0000-0001-6101-2855
Daniel P WindredSchool of Psychological Sciences Turner Institute for Brain and Mental Health, Monash University Melbourne Victoria Australia.ORCID 0000-0002-7461-7498
Angus BurnsBroad Institute Cambridge MA.
Samuel E JonesInstitute for Molecular Medicine Finland (FIMM) University of Helsinki Finland.ORCID 0000-0003-0153-922X
Tamar SoferDivision of Sleep and Circadian Disorders Brigham and Women's Hospital Boston MA.ORCID 0000-0001-8520-8860
Shaun M PurcellDivision of Sleep and Circadian Disorders Brigham and Women's Hospital Boston MA.ORCID 0000-0002-7402-5812
Xiaofeng ZhuDepartment of Population and Quantitative Health Sciences Case Western Reserve University Cleveland OH.
Hanna M OllilaBroad Institute Cambridge MA.
Simon D KyleSleep and Circadian Neuroscience Institute, Nuffield Department of Clinical Neurosciences University of Oxford United Kingdom.
Kai SpiegelhalderDepartment of Psychiatry and Psychotherapy Medical Centre-University of Freiburg, Faculty of Medicine, University of Freiburg Freiburg Germany.
Yuksel PekerDivision of Sleep and Circadian Disorders Brigham and Women's Hospital Boston MA.ORCID 0000-0001-9067-6538
Tianyi HuangDepartment of Neurology and Medicine Harvard Medical School, Brigham and Women's Hospital Boston MA.ORCID 0000-0001-8420-9167
Sean W CainSchool of Psychological Sciences Turner Institute for Brain and Mental Health, Monash University Melbourne Victoria Australia.ORCID 0000-0002-8385-1550
Andrew J K PhillipsSchool of Psychological Sciences Turner Institute for Brain and Mental Health, Monash University Melbourne Victoria Australia.ORCID 0000-0003-1156-7056
Richa SaxenaBroad Institute Cambridge MA.ORCID 0000-0003-2233-1065
Martin K RutterDivision of Endocrinology, Diabetes & Gastroenterology, School of Medical Sciences, Faculty of Biology, Medicine and Health University of Manchester Manchester United Kingdom.ORCID 0000-0001-6380-539X
Susan RedlineDivision of Sleep and Circadian Disorders Brigham and Women's Hospital Boston MA.ORCID 0000-0002-6585-1610
Heming WangDivision of Sleep and Circadian Disorders Brigham and Women's Hospital Boston MA.ORCID 0000-0002-1486-7495
Broad Institute · USBrigham and Women's Hospital · USMonash University · AUCase Western Reserve University · USManchester Academic Health Science Centre · GBNeurosciences Institute · USUniversity of Freiburg · DEUniversity of Helsinki · FI

Funding

Phenotypic and Molecular Signatures for Sleep Apnea and Related MorbiditiesR35HL135818 · NHLBI · BRIGHAM AND WOMEN'S HOSPITAL · PI Susan S. Redline · 2022 to 2023
$2.0M
Dissecting heterogeneity of excessive daytime sleepiness and impact on cardiovascular diseasesR01HL153814 · BRIGHAM AND WOMEN'S HOSPITAL · 2025 to 2025
$403k
NHLBI NIH HHS R01 HL153814NHLBI NIH HHS R21 HL165324NHLBI NIH HHS R35 HL135818
6 · The paper itself

Abstract

backgroundExcessive daytime sleepiness (EDS), experienced in 10% to 20% of the population, has been associated with cardiovascular disease and death. However, the condition is heterogeneous and is prevalent in individuals having short and long sleep duration. We sought to clarify the relationship between sleep duration subtypes of EDS with cardiovascular outcomes, accounting for these subtypes. METHODS AND

resultsWe defined 3 sleep duration subtypes of excessive daytime sleepiness: normal (6-9 hours), short (<6 hours), and long (>9 hours), and compared these with a nonsleepy, normal-sleep-duration reference group. We analyzed their associations with incident myocardial infarction (MI) and stroke using medical records of 355 901 UK Biobank participants and performed 2-sample Mendelian randomization for each outcome. Compared with healthy sleep, long-sleep EDS was associated with an 83% increased rate of MI (hazard ratio, 1.83 [95% CI, 1.21-2.77]) during 8.2-year median follow-up, adjusting for multiple health and sociodemographic factors. Mendelian randomization analysis provided supporting evidence of a causal role for a genetic long-sleep EDS subtype in MI (inverse-variance weighted β=1.995,

conclusionsOur study suggests the previous evidence linking EDS with increased cardiovascular disease risk may be primarily driven by the effect of its long-sleep subtype on higher risk of MI. Underlying mechanisms remain to be investigated but may involve sleep irregularity and circadian disruption, suggesting a need for novel interventions in this population.

Indexed as

Cardiovascular DiseasesDisorders of Excessive SomnolenceMyocardial InfarctionStrokeHumansSleepcardiovascular diseasesexcessive daytime sleepiness subtypesMendelian randomizationprospective analysissleep duration

Identifiers

PMID38084713
PMCPMC10863774
OpenAlexW4389624883

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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 Socratic graph.