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Patient clusters based on HbA1c trajectories: A step toward individualized medicine in type 2 diabetes
AIMS: To identify clinically meaningful clusters of patients with similar glycated hemoglobin (HbA1c) trajectories among patients with type 2 diabetes. METHODS: A retrospective cohort study using unsupervised machine learning clustering methodologies to determine clusters of patients with similar lo...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6235308/ https://www.ncbi.nlm.nih.gov/pubmed/30427908 http://dx.doi.org/10.1371/journal.pone.0207096 |
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author | Karpati, Tomas Leventer-Roberts, Maya Feldman, Becca Cohen-Stavi, Chandra Raz, Itamar Balicer, Ran |
author_facet | Karpati, Tomas Leventer-Roberts, Maya Feldman, Becca Cohen-Stavi, Chandra Raz, Itamar Balicer, Ran |
author_sort | Karpati, Tomas |
collection | PubMed |
description | AIMS: To identify clinically meaningful clusters of patients with similar glycated hemoglobin (HbA1c) trajectories among patients with type 2 diabetes. METHODS: A retrospective cohort study using unsupervised machine learning clustering methodologies to determine clusters of patients with similar longitudinal HbA1c trajectories. Stability of these clusters was assessed and supervised random forest analysis verified the clusters’ reproducibility. Clinical relevance of the clusters was assessed through multivariable analysis, comparing differences in risk for a composite outcome (macrovascular and microvascular outcomes, hypoglycemic events, and all-cause mortality) at HbA1c thresholds for each cluster. RESULTS: Among 60,423 patients, three clusters of HbA1c trajectories were generated: stable (n = 45,679), descending (n = 6,084), and ascending (n = 8,660) trends, which were reproduced with 99.8% accuracy using a random forest model. In the clinical relevance assessment, HbA1c levels demonstrated a J-shape association with the risk for outcomes. HbA1c level thresholds for minimizing outcomes’ risk differed by cluster: 6.0–6.4% for the stable cluster, <8.0% for the descending cluster, and <9.0 for the ascending cluster. CONCLUSIONS: By applying unsupervised machine learning to longitudinal HbA1c trajectories, we have identified clusters of patients who have distinct risk for diabetes-related complications. These clusters can be the basis for developing individualized models to personalize glycemic targets. |
format | Online Article Text |
id | pubmed-6235308 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-62353082018-12-01 Patient clusters based on HbA1c trajectories: A step toward individualized medicine in type 2 diabetes Karpati, Tomas Leventer-Roberts, Maya Feldman, Becca Cohen-Stavi, Chandra Raz, Itamar Balicer, Ran PLoS One Research Article AIMS: To identify clinically meaningful clusters of patients with similar glycated hemoglobin (HbA1c) trajectories among patients with type 2 diabetes. METHODS: A retrospective cohort study using unsupervised machine learning clustering methodologies to determine clusters of patients with similar longitudinal HbA1c trajectories. Stability of these clusters was assessed and supervised random forest analysis verified the clusters’ reproducibility. Clinical relevance of the clusters was assessed through multivariable analysis, comparing differences in risk for a composite outcome (macrovascular and microvascular outcomes, hypoglycemic events, and all-cause mortality) at HbA1c thresholds for each cluster. RESULTS: Among 60,423 patients, three clusters of HbA1c trajectories were generated: stable (n = 45,679), descending (n = 6,084), and ascending (n = 8,660) trends, which were reproduced with 99.8% accuracy using a random forest model. In the clinical relevance assessment, HbA1c levels demonstrated a J-shape association with the risk for outcomes. HbA1c level thresholds for minimizing outcomes’ risk differed by cluster: 6.0–6.4% for the stable cluster, <8.0% for the descending cluster, and <9.0 for the ascending cluster. CONCLUSIONS: By applying unsupervised machine learning to longitudinal HbA1c trajectories, we have identified clusters of patients who have distinct risk for diabetes-related complications. These clusters can be the basis for developing individualized models to personalize glycemic targets. Public Library of Science 2018-11-14 /pmc/articles/PMC6235308/ /pubmed/30427908 http://dx.doi.org/10.1371/journal.pone.0207096 Text en © 2018 Karpati et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Karpati, Tomas Leventer-Roberts, Maya Feldman, Becca Cohen-Stavi, Chandra Raz, Itamar Balicer, Ran Patient clusters based on HbA1c trajectories: A step toward individualized medicine in type 2 diabetes |
title | Patient clusters based on HbA1c trajectories: A step toward individualized medicine in type 2 diabetes |
title_full | Patient clusters based on HbA1c trajectories: A step toward individualized medicine in type 2 diabetes |
title_fullStr | Patient clusters based on HbA1c trajectories: A step toward individualized medicine in type 2 diabetes |
title_full_unstemmed | Patient clusters based on HbA1c trajectories: A step toward individualized medicine in type 2 diabetes |
title_short | Patient clusters based on HbA1c trajectories: A step toward individualized medicine in type 2 diabetes |
title_sort | patient clusters based on hba1c trajectories: a step toward individualized medicine in type 2 diabetes |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6235308/ https://www.ncbi.nlm.nih.gov/pubmed/30427908 http://dx.doi.org/10.1371/journal.pone.0207096 |
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