Evidence map›Paper›PMID 32795252›Full record

ArticleBMC cardiovascular disorders2020

Identifying Phenogroups in patients with subclinical diastolic dysfunction using unsupervised statistical learning.

Yvonne E Kaptein, Ilya Karagodin, Hongquan Zuo, Yu Lu, Jun Zhang, John S Kaptein, Jennifer L Strande

Open access · goldAbstract read
In one paragraph

Article in BMC cardiovascular disorders, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
2.4field-weighted citation impact, top 9% 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

11 citing papers in PubMed, 21 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

7 authors at 5 institutions in 1 country.

Yvonne E KapteinAurora Cardiovascular Services, Aurora St Luke's Medical Center, Milwaukee, WI, USA. yvonne.kaptein@gmail.com.
Ilya KaragodinDepartment of Medicine, University of Chicago, Chicago, USA.
Hongquan ZuoElectrical Engineering and Computer Science, University of Wisconsin-Milwaukee, Milwaukee, USA.
Yu LuElectrical Engineering and Computer Science, University of Wisconsin-Milwaukee, Milwaukee, USA.
Jun ZhangElectrical Engineering and Computer Science, University of Wisconsin-Milwaukee, Milwaukee, USA.
John S KapteinUniversity of Southern California, Los Angeles, USA.
Jennifer L StrandeDepartment of Medicine, Medical College of Wisconsin, Milwaukee, USA.
University of Wisconsin–Milwaukee · USAurora St. Luke's Medical Center · USMedical College of Wisconsin · USUniversity of Chicago · USUniversity of Southern California · US

Funding

MULTIDISCIPLINARY CARDIAC SCIENCEST32HL007381 · NHLBI · UNIVERSITY OF CHICAGO · PI JEANNE M DECARA, Yoav Gilad · 1985 to 2026
$12.5M
Developing nicorandil and companion biomarkers for DMD cardiomyopathy therapyR01HL134932 · NHLBI · MEDICAL COLLEGE OF WISCONSIN · PI LAWLOR, MICHAEL WILLIAM · 2017 to 2020
$1.8M
NHLBI NIH HHS R01 HL134932NHLBI NIH HHS T32 HL007381NIH HHS HL134932
6 · The paper itself

Abstract

backgroundSubclinical diastolic dysfunction is a precursor for developing heart failure with preserved ejection fraction (HFpEF); yet not all patients progress to HFpEF. Our objective was to evaluate clinical and echocardiographic variables to identify patients who develop HFpEF.

methodsClinical, laboratory, and echocardiographic data were retrospectively collected for 81 patients without HF and 81 matched patients with HFpEF at the time of first documentation of subclinical diastolic dysfunction. Density-based clustering or hierarchical clustering to group patients was based on 65 total variables including 19 categorical and 46 numerical variables. Logistic regression analysis was conducted on the entire study population as well as each individual cluster to identify independent predictors of HFpEF.

resultsUnsupervised clustering identified 3 subgroups which differed in gender composition, severity of cardiac hypertrophy and aortic stenosis, NT-proBNP, percentage of patients who progressed to HFpEF, and timing of disease progression from diastolic dysfunction to HFpEF to death. Clusters that had higher percentages of women had progressively milder cardiac hypertrophy, less severe aortic stenosis, lower NT-proBNP, were diagnosed at an older age with HFpEF, and survived to an older age. Independent predictors of HFpEF for the entire cohort included diabetes, chronic kidney disease, atrial fibrillation, and diuretic use, with additional predictive variables found for each cluster.

conclusionsCluster analysis can identify phenotypically distinct subgroups of patients with diastolic dysfunction. Clusters differ in HFpEF and mortality outcome. In addition, the variables that correlate with and predict HFpEF outcome differ among clusters.

Indexed as

Deep LearningDiagnosis, Computer-AssistedStroke VolumeUnsupervised Machine LearningVentricular Function, LeftAgedAged, 80 and overAsymptomatic DiseasesBiomarkersCluster AnalysisDiastoleDisease ProgressionEchocardiographyFemaleHeart FailureHumansBiomarkersNatriuretic Peptide, BrainPeptide Fragmentspro-brain natriuretic peptide (1-76)Clinical studiesDiastolic dysfunctionEchocardiographyHeart failureHeart failure with preserved ejection fractionHierarchical clusteringRisk factorsUnsupervised machine learning

Identifiers

PMID32795252
PMCPMC7427922
OpenAlexW3049346026

What OpenQuestion holds

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LicenceCC BY
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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.