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Identifying Phenogroups in patients with subclinical diastolic dysfunction using unsupervised statistical learning
BACKGROUND: Subclinical 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. METHODS: Clinical...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7427922/ https://www.ncbi.nlm.nih.gov/pubmed/32795252 http://dx.doi.org/10.1186/s12872-020-01620-z |
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author | Kaptein, Yvonne E. Karagodin, Ilya Zuo, Hongquan Lu, Yu Zhang, Jun Kaptein, John S. Strande, Jennifer L. |
author_facet | Kaptein, Yvonne E. Karagodin, Ilya Zuo, Hongquan Lu, Yu Zhang, Jun Kaptein, John S. Strande, Jennifer L. |
author_sort | Kaptein, Yvonne E. |
collection | PubMed |
description | BACKGROUND: Subclinical 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. METHODS: Clinical, 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. RESULTS: Unsupervised 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. CONCLUSIONS: Cluster 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. |
format | Online Article Text |
id | pubmed-7427922 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-74279222020-08-17 Identifying Phenogroups in patients with subclinical diastolic dysfunction using unsupervised statistical learning Kaptein, Yvonne E. Karagodin, Ilya Zuo, Hongquan Lu, Yu Zhang, Jun Kaptein, John S. Strande, Jennifer L. BMC Cardiovasc Disord Research Article BACKGROUND: Subclinical 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. METHODS: Clinical, 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. RESULTS: Unsupervised 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. CONCLUSIONS: Cluster 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. BioMed Central 2020-08-14 /pmc/articles/PMC7427922/ /pubmed/32795252 http://dx.doi.org/10.1186/s12872-020-01620-z Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Article Kaptein, Yvonne E. Karagodin, Ilya Zuo, Hongquan Lu, Yu Zhang, Jun Kaptein, John S. Strande, Jennifer L. Identifying Phenogroups in patients with subclinical diastolic dysfunction using unsupervised statistical learning |
title | Identifying Phenogroups in patients with subclinical diastolic dysfunction using unsupervised statistical learning |
title_full | Identifying Phenogroups in patients with subclinical diastolic dysfunction using unsupervised statistical learning |
title_fullStr | Identifying Phenogroups in patients with subclinical diastolic dysfunction using unsupervised statistical learning |
title_full_unstemmed | Identifying Phenogroups in patients with subclinical diastolic dysfunction using unsupervised statistical learning |
title_short | Identifying Phenogroups in patients with subclinical diastolic dysfunction using unsupervised statistical learning |
title_sort | identifying phenogroups in patients with subclinical diastolic dysfunction using unsupervised statistical learning |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7427922/ https://www.ncbi.nlm.nih.gov/pubmed/32795252 http://dx.doi.org/10.1186/s12872-020-01620-z |
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