Evidence map›Paper›PMID 36587059›Full record

ArticleScientific reports2022

Deep learning-derived cardiovascular age shares a genetic basis with other cardiac phenotypes.

Julian Libiseller-Egger, Jody E Phelan, Zachi I Attia, Ernest Diez Benavente, Susana Campino, Paul A Friedman, Francisco Lopez-Jimenez, David A Leon, Taane G Clark

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
5.6field-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

14 citing papers in PubMed, 31 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Review
  5. Article
  6. Article
  7. Article
  8. Genetics of Cardiac Aging Implicate Organ-Specific Variation.medRxiv : the preprint server for health sciences · 2024
    Article
  9. Article
  10. Article
  11. Review
  12. The Potential for Artificial Intelligence Applied to Epigenetics.Mayo Clinic proceedings. Digital health · 2023
    Article
  13. Review
  14. 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 4 countries.

Julian Libiseller-EggerFaculty of Infectious and Tropical Diseases, London School of Hygiene & Tropical Medicine, London, UK.
Jody E PhelanFaculty of Infectious and Tropical Diseases, London School of Hygiene & Tropical Medicine, London, UK.
Zachi I AttiaDepartment of Cardiovascular Medicine, Mayo Clinic College of Medicine, Rochester, MN, USA.
Ernest Diez BenaventeFaculty of Infectious and Tropical Diseases, London School of Hygiene & Tropical Medicine, London, UK.
Susana CampinoFaculty of Infectious and Tropical Diseases, London School of Hygiene & Tropical Medicine, London, UK.
Paul A FriedmanDepartment of Cardiovascular Medicine, Mayo Clinic College of Medicine, Rochester, MN, USA.
Francisco Lopez-JimenezDepartment of Cardiovascular Medicine, Mayo Clinic College of Medicine, Rochester, MN, USA.
David A LeonFaculty of Epidemiology and Population Health, London School of Hygiene & Tropical Medicine, London, UK.
Taane G ClarkFaculty of Infectious and Tropical Diseases, London School of Hygiene & Tropical Medicine, London, UK. taane.clark@lshtm.ac.uk.
London School of Hygiene & Tropical Medicine · GBMayo Clinic · USUniversity Medical Center Utrecht · NL

Funding

Medical Research Council MC_PC_17228Medical Research Council MR/M01360X/1Medical Research Council MR/N010469/1Medical Research Council MR/R020973/1Medical Research Council MR/R025576/1Medical Research Council MR/X005895/1Wellcome Trust
6 · The paper itself

Abstract

Artificial intelligence (AI)-based approaches can now use electrocardiograms (ECGs) to provide expert-level performance in detecting heart abnormalities and diagnosing disease. Additionally, patient age predicted from ECGs by AI models has shown great potential as a biomarker for cardiovascular age, where recent work has found its deviation from chronological age ("delta age") to be associated with mortality and co-morbidities. However, despite being crucial for understanding underlying individual risk, the genetic underpinning of delta age is unknown. In this work we performed a genome-wide association study using UK Biobank data (n=34,432) and identified eight loci associated with delta age ([Formula: see text]), including genes linked to cardiovascular disease (CVD) (e.g. SCN5A) and (heart) muscle development (e.g. TTN). Our results indicate that the genetic basis of cardiovascular ageing is predominantly determined by genes directly involved with the cardiovascular system rather than those connected to more general mechanisms of ageing. Our insights inform the epidemiology of CVD, with implications for preventative and precision medicine.

Indexed as

Cardiovascular DiseasesDeep LearningArtificial IntelligenceGenome-Wide Association StudyHeartHumansPhenotype

Identifiers

PMID36587059
PMCPMC9805465
OpenAlexW4313397186

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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.