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Predicting clinical events using Bayesian multivariate linear mixed models with application to scleroderma
BACKGROUND: Scleroderma is a serious chronic autoimmune disease in which a patient’s disease state manifests in several irregularly spaced longitudinal measures of lung, heart, skin, and other organ systems. Threshold crossings of pulmonary and cardiac measures indicate potentially life-threatening...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8590788/ https://www.ncbi.nlm.nih.gov/pubmed/34773969 http://dx.doi.org/10.1186/s12874-021-01439-y |
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author | Kim, Ji Soo Shah, Ami A. Hummers, Laura K. Zeger, Scott L. |
author_facet | Kim, Ji Soo Shah, Ami A. Hummers, Laura K. Zeger, Scott L. |
author_sort | Kim, Ji Soo |
collection | PubMed |
description | BACKGROUND: Scleroderma is a serious chronic autoimmune disease in which a patient’s disease state manifests in several irregularly spaced longitudinal measures of lung, heart, skin, and other organ systems. Threshold crossings of pulmonary and cardiac measures indicate potentially life-threatening key clinical events including interstitial lung disease (ILD), cardiomyopathy, and pulmonary hypertension (PH). The statistical challenge is to accurately and precisely predict these events by using all of the clinical history for the patient at hand and for a reference population of patients. METHODS: We use a Bayesian mixed model approach to simultaneously characterize each individual’s future trajectories for several biomarkers. We estimate this model using a large population of patients from the Johns Hopkins Scleroderma Center Research Registry. The joint probabilities of critical lung and heart events are then calculated as a byproduct of the mixed model. RESULTS: The performance of this approach is substantially better than standard, more common alternatives. In order to predict an individual’s risks in a clinical setting, we also develop a cross-validated, sequential prediction (CVSP) algorithm. As additional data are observed during a patient’s visit, the algorithm sequentially produces updated predictions for the future longitudinal trajectories and for ILD, cardiomyopathy, and PH. The updated prediction distributions with little additional computing, for example within an electronic health record (EHR). CONCLUSIONS: This method that generates real-time personalized risk estimates has been implemented within the electronic health record system for clinical testing. To our knowledge, this work represents the first approach to compute personalized risk estimates for multiple scleroderma complications. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12874-021-01439-y. |
format | Online Article Text |
id | pubmed-8590788 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-85907882021-11-15 Predicting clinical events using Bayesian multivariate linear mixed models with application to scleroderma Kim, Ji Soo Shah, Ami A. Hummers, Laura K. Zeger, Scott L. BMC Med Res Methodol Research BACKGROUND: Scleroderma is a serious chronic autoimmune disease in which a patient’s disease state manifests in several irregularly spaced longitudinal measures of lung, heart, skin, and other organ systems. Threshold crossings of pulmonary and cardiac measures indicate potentially life-threatening key clinical events including interstitial lung disease (ILD), cardiomyopathy, and pulmonary hypertension (PH). The statistical challenge is to accurately and precisely predict these events by using all of the clinical history for the patient at hand and for a reference population of patients. METHODS: We use a Bayesian mixed model approach to simultaneously characterize each individual’s future trajectories for several biomarkers. We estimate this model using a large population of patients from the Johns Hopkins Scleroderma Center Research Registry. The joint probabilities of critical lung and heart events are then calculated as a byproduct of the mixed model. RESULTS: The performance of this approach is substantially better than standard, more common alternatives. In order to predict an individual’s risks in a clinical setting, we also develop a cross-validated, sequential prediction (CVSP) algorithm. As additional data are observed during a patient’s visit, the algorithm sequentially produces updated predictions for the future longitudinal trajectories and for ILD, cardiomyopathy, and PH. The updated prediction distributions with little additional computing, for example within an electronic health record (EHR). CONCLUSIONS: This method that generates real-time personalized risk estimates has been implemented within the electronic health record system for clinical testing. To our knowledge, this work represents the first approach to compute personalized risk estimates for multiple scleroderma complications. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12874-021-01439-y. BioMed Central 2021-11-14 /pmc/articles/PMC8590788/ /pubmed/34773969 http://dx.doi.org/10.1186/s12874-021-01439-y Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://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 Kim, Ji Soo Shah, Ami A. Hummers, Laura K. Zeger, Scott L. Predicting clinical events using Bayesian multivariate linear mixed models with application to scleroderma |
title | Predicting clinical events using Bayesian multivariate linear mixed models with application to scleroderma |
title_full | Predicting clinical events using Bayesian multivariate linear mixed models with application to scleroderma |
title_fullStr | Predicting clinical events using Bayesian multivariate linear mixed models with application to scleroderma |
title_full_unstemmed | Predicting clinical events using Bayesian multivariate linear mixed models with application to scleroderma |
title_short | Predicting clinical events using Bayesian multivariate linear mixed models with application to scleroderma |
title_sort | predicting clinical events using bayesian multivariate linear mixed models with application to scleroderma |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8590788/ https://www.ncbi.nlm.nih.gov/pubmed/34773969 http://dx.doi.org/10.1186/s12874-021-01439-y |
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