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Development and validation of machine learning for early mortality in systemic sclerosis

Clinical predictors of mortality in systemic sclerosis (SSc) are diversely reported due to different healthcare conditions and populations. A simple predictive model for early mortality among patients with SSc is needed as a precise referral tool for general practitioners. We aimed to develop and va...

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Autores principales: Foocharoen, Chingching, Thinkhamrop, Wilaiphorn, Chaichaya, Nathaphop, Mahakkanukrauh, Ajanee, Suwannaroj, Siraphop, Thinkhamrop, Bandit
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9563044/
https://www.ncbi.nlm.nih.gov/pubmed/36229500
http://dx.doi.org/10.1038/s41598-022-22161-9
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author Foocharoen, Chingching
Thinkhamrop, Wilaiphorn
Chaichaya, Nathaphop
Mahakkanukrauh, Ajanee
Suwannaroj, Siraphop
Thinkhamrop, Bandit
author_facet Foocharoen, Chingching
Thinkhamrop, Wilaiphorn
Chaichaya, Nathaphop
Mahakkanukrauh, Ajanee
Suwannaroj, Siraphop
Thinkhamrop, Bandit
author_sort Foocharoen, Chingching
collection PubMed
description Clinical predictors of mortality in systemic sclerosis (SSc) are diversely reported due to different healthcare conditions and populations. A simple predictive model for early mortality among patients with SSc is needed as a precise referral tool for general practitioners. We aimed to develop and validate a simple predictive model for predicting mortality among patients with SSc. Prognostic research with a historical cohort study design was conducted between January 1, 2013, and December 31, 2020, in adult SSc patients attending the Scleroderma Clinic at a university hospital in Thailand. The data were extracted from the Scleroderma Registry Database. Early mortality was defined as dying within 5 years after the onset of SSc. Deep learning algorithms with Adam optimizer and different machine learning algorithms (including Logistic Regression, Decision tree, AdaBoost, Random Forest, Gradient Boosting, XGBoost, and Autoencoder neural network) were used to classify SSc mortality. In addition, the model’s performance was evaluated using the area under the receiver operating characteristic curve (auROC) and its 95% confidence interval (CI) and values in the confusion matrix. The predictive model development included 528 SSc patients, 343 (65.0%) were females and 374 (70.8%) had dcSSc. Ninety-five died within 5 years after disease onset. The final 2 models with the highest predictive performance comprise the modified Rodnan skin score (mRSS) and the WHO-FC ≥ II for Model 1 and mRSS and WHO-FC ≥ III for Model 2. Model 1 provided the highest predictive performance, followed by Model 2. After internal validation, the accuracy and auROC were good. The specificity was high in Models 1 and 2 (84.8%, 89.8%, and 98.8% in model 1 vs. 84.8%, 85.6%, and 98.8% in model 2). This simplified machine learning model for predicting early mortality among patients with SSc could guide early referrals to specialists and help rheumatologists with close monitoring and management planning. External validation across multi-SSc clinics should be considered for further study.
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spelling pubmed-95630442022-10-15 Development and validation of machine learning for early mortality in systemic sclerosis Foocharoen, Chingching Thinkhamrop, Wilaiphorn Chaichaya, Nathaphop Mahakkanukrauh, Ajanee Suwannaroj, Siraphop Thinkhamrop, Bandit Sci Rep Article Clinical predictors of mortality in systemic sclerosis (SSc) are diversely reported due to different healthcare conditions and populations. A simple predictive model for early mortality among patients with SSc is needed as a precise referral tool for general practitioners. We aimed to develop and validate a simple predictive model for predicting mortality among patients with SSc. Prognostic research with a historical cohort study design was conducted between January 1, 2013, and December 31, 2020, in adult SSc patients attending the Scleroderma Clinic at a university hospital in Thailand. The data were extracted from the Scleroderma Registry Database. Early mortality was defined as dying within 5 years after the onset of SSc. Deep learning algorithms with Adam optimizer and different machine learning algorithms (including Logistic Regression, Decision tree, AdaBoost, Random Forest, Gradient Boosting, XGBoost, and Autoencoder neural network) were used to classify SSc mortality. In addition, the model’s performance was evaluated using the area under the receiver operating characteristic curve (auROC) and its 95% confidence interval (CI) and values in the confusion matrix. The predictive model development included 528 SSc patients, 343 (65.0%) were females and 374 (70.8%) had dcSSc. Ninety-five died within 5 years after disease onset. The final 2 models with the highest predictive performance comprise the modified Rodnan skin score (mRSS) and the WHO-FC ≥ II for Model 1 and mRSS and WHO-FC ≥ III for Model 2. Model 1 provided the highest predictive performance, followed by Model 2. After internal validation, the accuracy and auROC were good. The specificity was high in Models 1 and 2 (84.8%, 89.8%, and 98.8% in model 1 vs. 84.8%, 85.6%, and 98.8% in model 2). This simplified machine learning model for predicting early mortality among patients with SSc could guide early referrals to specialists and help rheumatologists with close monitoring and management planning. External validation across multi-SSc clinics should be considered for further study. Nature Publishing Group UK 2022-10-13 /pmc/articles/PMC9563044/ /pubmed/36229500 http://dx.doi.org/10.1038/s41598-022-22161-9 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/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 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/) .
spellingShingle Article
Foocharoen, Chingching
Thinkhamrop, Wilaiphorn
Chaichaya, Nathaphop
Mahakkanukrauh, Ajanee
Suwannaroj, Siraphop
Thinkhamrop, Bandit
Development and validation of machine learning for early mortality in systemic sclerosis
title Development and validation of machine learning for early mortality in systemic sclerosis
title_full Development and validation of machine learning for early mortality in systemic sclerosis
title_fullStr Development and validation of machine learning for early mortality in systemic sclerosis
title_full_unstemmed Development and validation of machine learning for early mortality in systemic sclerosis
title_short Development and validation of machine learning for early mortality in systemic sclerosis
title_sort development and validation of machine learning for early mortality in systemic sclerosis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9563044/
https://www.ncbi.nlm.nih.gov/pubmed/36229500
http://dx.doi.org/10.1038/s41598-022-22161-9
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