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Nationwide prediction of type 2 diabetes comorbidities
Identification of individuals at risk of developing disease comorbidities represents an important task in tackling the growing personal and societal burdens associated with chronic diseases. We employed machine learning techniques to investigate to what extent data from longitudinal, nationwide Dani...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7000818/ https://www.ncbi.nlm.nih.gov/pubmed/32019971 http://dx.doi.org/10.1038/s41598-020-58601-7 |
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author | Dworzynski, Piotr Aasbrenn, Martin Rostgaard, Klaus Melbye, Mads Gerds, Thomas Alexander Hjalgrim, Henrik Pers, Tune H. |
author_facet | Dworzynski, Piotr Aasbrenn, Martin Rostgaard, Klaus Melbye, Mads Gerds, Thomas Alexander Hjalgrim, Henrik Pers, Tune H. |
author_sort | Dworzynski, Piotr |
collection | PubMed |
description | Identification of individuals at risk of developing disease comorbidities represents an important task in tackling the growing personal and societal burdens associated with chronic diseases. We employed machine learning techniques to investigate to what extent data from longitudinal, nationwide Danish health registers can be used to predict individuals at high risk of developing type 2 diabetes (T2D) comorbidities. Leveraging logistic regression-, random forest- and gradient boosting models and register data spanning hospitalizations, drug prescriptions and contacts with primary care contractors from >200,000 individuals newly diagnosed with T2D, we predicted five-year risk of heart failure (HF), myocardial infarction (MI), stroke (ST), cardiovascular disease (CVD) and chronic kidney disease (CKD). For HF, MI, CVD, and CKD, register-based models outperformed a reference model leveraging canonical individual characteristics by achieving area under the receiver operating characteristic curve improvements of 0.06, 0.03, 0.04, and 0.07, respectively. The top 1,000 patients predicted to be at highest risk exhibited observed incidence ratios exceeding 4.99, 3.52, 1.97 and 4.71 respectively. In summary, prediction of T2D comorbidities utilizing Danish registers led to consistent albeit modest performance improvements over reference models, suggesting that register data could be leveraged to systematically identify individuals at risk of developing disease comorbidities. |
format | Online Article Text |
id | pubmed-7000818 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-70008182020-02-11 Nationwide prediction of type 2 diabetes comorbidities Dworzynski, Piotr Aasbrenn, Martin Rostgaard, Klaus Melbye, Mads Gerds, Thomas Alexander Hjalgrim, Henrik Pers, Tune H. Sci Rep Article Identification of individuals at risk of developing disease comorbidities represents an important task in tackling the growing personal and societal burdens associated with chronic diseases. We employed machine learning techniques to investigate to what extent data from longitudinal, nationwide Danish health registers can be used to predict individuals at high risk of developing type 2 diabetes (T2D) comorbidities. Leveraging logistic regression-, random forest- and gradient boosting models and register data spanning hospitalizations, drug prescriptions and contacts with primary care contractors from >200,000 individuals newly diagnosed with T2D, we predicted five-year risk of heart failure (HF), myocardial infarction (MI), stroke (ST), cardiovascular disease (CVD) and chronic kidney disease (CKD). For HF, MI, CVD, and CKD, register-based models outperformed a reference model leveraging canonical individual characteristics by achieving area under the receiver operating characteristic curve improvements of 0.06, 0.03, 0.04, and 0.07, respectively. The top 1,000 patients predicted to be at highest risk exhibited observed incidence ratios exceeding 4.99, 3.52, 1.97 and 4.71 respectively. In summary, prediction of T2D comorbidities utilizing Danish registers led to consistent albeit modest performance improvements over reference models, suggesting that register data could be leveraged to systematically identify individuals at risk of developing disease comorbidities. Nature Publishing Group UK 2020-02-04 /pmc/articles/PMC7000818/ /pubmed/32019971 http://dx.doi.org/10.1038/s41598-020-58601-7 Text en © The Author(s) 2020 Open Access This 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Dworzynski, Piotr Aasbrenn, Martin Rostgaard, Klaus Melbye, Mads Gerds, Thomas Alexander Hjalgrim, Henrik Pers, Tune H. Nationwide prediction of type 2 diabetes comorbidities |
title | Nationwide prediction of type 2 diabetes comorbidities |
title_full | Nationwide prediction of type 2 diabetes comorbidities |
title_fullStr | Nationwide prediction of type 2 diabetes comorbidities |
title_full_unstemmed | Nationwide prediction of type 2 diabetes comorbidities |
title_short | Nationwide prediction of type 2 diabetes comorbidities |
title_sort | nationwide prediction of type 2 diabetes comorbidities |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7000818/ https://www.ncbi.nlm.nih.gov/pubmed/32019971 http://dx.doi.org/10.1038/s41598-020-58601-7 |
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