Evidence map›Paper›PMID 34845917›Full record

ArticleJournal of the American Heart Association2021

Unsupervised Learning for Automated Detection of Coronary Artery Disease Subgroups.

Alyssa M Flores, Alejandro Schuler, Anne Verena Eberhard, Jeffrey W Olin, John P Cooke, Nicholas J Leeper, Nigam H Shah, Elsie G Ross

Registry-linked trialAbstract read
In one paragraph

Article in Journal of the American Heart Association, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT00380185 (The Genetic Determinants of Peripheral Arterial Disease), which is not on this map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing 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.

NCT00380185 completednot on this map

The Genetic Determinants of Peripheral Arterial Disease

TypeobservationalSponsorStanford UniversityRan2004Enrolled1,789ConditionsPeripheral Vascular Diseases
3 · Its place in the literature

Who cites it

21 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
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  11. Article
  12. Review
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  15. Review
  16. Article
  17. Phenomics and Robust Multiomics Data for Cardiovascular Disease Subtyping.Arteriosclerosis, thrombosis, and vascular biology · 2023
    Review
  18. Article
  19. Article
  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

8 authors.

Alyssa M FloresDivision of Vascular Surgery Department of Surgery Stanford University School of Medicine Stanford CA.ORCID 0000-0002-4623-5521
Alejandro SchulerCenter for Biomedical Informatics Research Stanford University Stanford CA.ORCID 0000-0003-4853-6130
Anne Verena EberhardDivision of Vascular Surgery Department of Surgery Stanford University School of Medicine Stanford CA.ORCID 0000-0002-3158-2686
Jeffrey W OlinZena and Michael A. Wiener Cardiovascular InstituteMarie-Josée and Henry R. Kravis Center for Cardiovascular HealthIcahn School of Medicine at Mount Sinai New York NY.ORCID 0000-0003-3374-616X
John P CookeDepartment of Cardiovascular Sciences Houston Methodist Research Institute Houston TX.ORCID 0000-0003-0033-9138
Nicholas J LeeperDivision of Vascular Surgery Department of Surgery Stanford University School of Medicine Stanford CA.ORCID 0000-0002-0905-2806
Nigam H ShahCenter for Biomedical Informatics Research Stanford University Stanford CA.ORCID 0000-0001-9385-7158
Elsie G RossDivision of Vascular Surgery Department of Surgery Stanford University School of Medicine Stanford CA.ORCID 0000-0002-9366-0109

Funding

Training In Cardiovascular Physiology & PharmacologyT32HL007444 · NHLBI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI Ju Chen, Robert Scott Ross · 1985 to 2026
$11.1M
Clonal expansion, resistance to efferocytosis and innate immunity in atherosclerosisR35HL144475 · NHLBI · STANFORD UNIVERSITY · PI LEEPER, NICHOLAS JAMES · 2019 to 2024
$5.1M
Methods for generalized ontology terms enrichment analysisR01LM011369 · NLM · STANFORD UNIVERSITY · PI SHAH, NIGAM H · 2013 to 2020
$5.0M
Genetic Determinants of PADR01HL075774 · NHLBI · STANFORD UNIVERSITY · PI COOKE, JOHN P · 2003 to 2007
$5.0M
Stanford Career Development in Vascular MedicineK12HL087746 · NHLBI · STANFORD UNIVERSITY · PI DALMAN, RONALD L · 2007 to 2012
$3.5M
UCSD PRIDE Faculty Development Program in Cardiovascular SciencesR25HL145817 · NHLBI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI Robert Scott Ross, Joann Trejo · 2019 to 2026
$3.3M
Using Artificial Intelligence to Enable Early Identification and Treatment of Peripheral Artery DiseaseK01HL148639 · NHLBI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI ROSS, ELSIE GYANG · 2019 to 2023
$807k
NHLBI NIH HHS K01 HL148639NHLBI NIH HHS K12 HL087746NHLBI NIH HHS R01 HL075774NHLBI NIH HHS R25 HL145817NHLBI NIH HHS R35 HL144475NHLBI NIH HHS T32 HL007444NLM NIH HHS R01 LM011369
6 · The paper itself

Abstract

Background The promise of precision population health includes the ability to use robust patient data to tailor prevention and care to specific groups. Advanced analytics may allow for automated detection of clinically informative subgroups that account for clinical, genetic, and environmental variability. This study sought to evaluate whether unsupervised machine learning approaches could interpret heterogeneous and missing clinical data to discover clinically important coronary artery disease subgroups. Methods and Results The Genetic Determinants of Peripheral Arterial Disease study is a prospective cohort that includes individuals with newly diagnosed and/or symptomatic coronary artery disease. We applied generalized low rank modeling and K-means cluster analysis using 155 phenotypic and genetic variables from 1329 participants. Cox proportional hazard models were used to examine associations between clusters and major adverse cardiovascular and cerebrovascular events and all-cause mortality. We then compared performance of risk stratification based on clusters and the American College of Cardiology/American Heart Association pooled cohort equations. Unsupervised analysis identified 4 phenotypically and prognostically distinct clusters. All-cause mortality was highest in cluster 1 (oldest/most comorbid; 26%), whereas major adverse cardiovascular and cerebrovascular event rates were highest in cluster 2 (youngest/multiethnic; 41%). Cluster 4 (middle-aged/healthiest behaviors) experienced more incident major adverse cardiovascular and cerebrovascular events (30%) than cluster 3 (middle-aged/lowest medication adherence; 23%), despite apparently similar risk factor and lifestyle profiles. In comparison with the pooled cohort equations, cluster membership was more informative for risk assessment of myocardial infarction, stroke, and mortality. Conclusions Unsupervised clustering identified 4 unique coronary artery disease subgroups with distinct clinical trajectories. Flexible unsupervised machine learning algorithms offer the ability to meaningfully process heterogeneous patient data and provide sharper insights into disease characterization and risk assessment. Registration URL: https://www.clinicaltrials.gov; Unique identifier: NCT00380185.

Indexed as

Coronary Artery DiseaseUnsupervised Machine LearningAdultAgedHumansMiddle AgedProspective StudiesRisk Assessmentcluster analysiscoronary artery diseasemachine learningphenotype discovery

Identifiers

PMID34845917
PMCPMC9075403

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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 Socratic graph.