Comparison of Machine Learning Models for Prediction of Initial Intravenous Immunoglobulin Resistance in Children With Kawasaki Disease

We constructed an optimal machine learning (ML) method for predicting intravenous immunoglobulin (IVIG) resistance in children with Kawasaki disease (KD) using commonly available clinical and laboratory variables. We retrospectively collected 98 clinical records of hospitalized children with KD (2–1...

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Main Authors: Yasutaka Kuniyoshi, Haruka Tokutake, Natsuki Takahashi, Azusa Kamura, Sumie Yasuda, Makoto Tashiro
Format: Article
Language:English
Published: Frontiers Media S.A. 2020-12-01
Series:Frontiers in Pediatrics
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fped.2020.570834/full
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spelling doaj-a603081bdf1b4f98b2ff4be9fb6b2a682020-12-08T08:35:33ZengFrontiers Media S.A.Frontiers in Pediatrics2296-23602020-12-01810.3389/fped.2020.570834570834Comparison of Machine Learning Models for Prediction of Initial Intravenous Immunoglobulin Resistance in Children With Kawasaki DiseaseYasutaka KuniyoshiHaruka TokutakeNatsuki TakahashiAzusa KamuraSumie YasudaMakoto TashiroWe constructed an optimal machine learning (ML) method for predicting intravenous immunoglobulin (IVIG) resistance in children with Kawasaki disease (KD) using commonly available clinical and laboratory variables. We retrospectively collected 98 clinical records of hospitalized children with KD (2–109 months of age). We found that 20 (20%) children were resistant to initial IVIG therapy. We trained three ML techniques, including logistic regression, linear support vector machine, and eXtreme gradient boosting with 10 variables against IVIG resistance. Moreover, we estimated the predictive performance based on nested 5-fold cross-validation (CV). We also selected variables using the recursive feature elimination method and performed the nested 5-fold CV with selected variables in a similar manner. We compared ML models with the existing system regardless of their predictive performance. Results of the area under the receiver operator characteristic curve were in the range of 0.58–0.60 in the all-variable model and 0.60–0.75 in the select model. The specificities were more than 0.90 and higher than those in existing scoring systems, but the sensitivities were lower. Three ML models based on demographics and routine laboratory variables did not provide reliable performance. This is possibly the first study that has attempted to establish a better predictive model. Additional biomarkers are probably needed to generate an effective prediction model.https://www.frontiersin.org/articles/10.3389/fped.2020.570834/fullarea under the curveextreme gradient boostingsupport vector machinelogistic regressionnested cross-validationpredictive model
collection DOAJ
language English
format Article
sources DOAJ
author Yasutaka Kuniyoshi
Haruka Tokutake
Natsuki Takahashi
Azusa Kamura
Sumie Yasuda
Makoto Tashiro
spellingShingle Yasutaka Kuniyoshi
Haruka Tokutake
Natsuki Takahashi
Azusa Kamura
Sumie Yasuda
Makoto Tashiro
Comparison of Machine Learning Models for Prediction of Initial Intravenous Immunoglobulin Resistance in Children With Kawasaki Disease
Frontiers in Pediatrics
area under the curve
extreme gradient boosting
support vector machine
logistic regression
nested cross-validation
predictive model
author_facet Yasutaka Kuniyoshi
Haruka Tokutake
Natsuki Takahashi
Azusa Kamura
Sumie Yasuda
Makoto Tashiro
author_sort Yasutaka Kuniyoshi
title Comparison of Machine Learning Models for Prediction of Initial Intravenous Immunoglobulin Resistance in Children With Kawasaki Disease
title_short Comparison of Machine Learning Models for Prediction of Initial Intravenous Immunoglobulin Resistance in Children With Kawasaki Disease
title_full Comparison of Machine Learning Models for Prediction of Initial Intravenous Immunoglobulin Resistance in Children With Kawasaki Disease
title_fullStr Comparison of Machine Learning Models for Prediction of Initial Intravenous Immunoglobulin Resistance in Children With Kawasaki Disease
title_full_unstemmed Comparison of Machine Learning Models for Prediction of Initial Intravenous Immunoglobulin Resistance in Children With Kawasaki Disease
title_sort comparison of machine learning models for prediction of initial intravenous immunoglobulin resistance in children with kawasaki disease
publisher Frontiers Media S.A.
series Frontiers in Pediatrics
issn 2296-2360
publishDate 2020-12-01
description We constructed an optimal machine learning (ML) method for predicting intravenous immunoglobulin (IVIG) resistance in children with Kawasaki disease (KD) using commonly available clinical and laboratory variables. We retrospectively collected 98 clinical records of hospitalized children with KD (2–109 months of age). We found that 20 (20%) children were resistant to initial IVIG therapy. We trained three ML techniques, including logistic regression, linear support vector machine, and eXtreme gradient boosting with 10 variables against IVIG resistance. Moreover, we estimated the predictive performance based on nested 5-fold cross-validation (CV). We also selected variables using the recursive feature elimination method and performed the nested 5-fold CV with selected variables in a similar manner. We compared ML models with the existing system regardless of their predictive performance. Results of the area under the receiver operator characteristic curve were in the range of 0.58–0.60 in the all-variable model and 0.60–0.75 in the select model. The specificities were more than 0.90 and higher than those in existing scoring systems, but the sensitivities were lower. Three ML models based on demographics and routine laboratory variables did not provide reliable performance. This is possibly the first study that has attempted to establish a better predictive model. Additional biomarkers are probably needed to generate an effective prediction model.
topic area under the curve
extreme gradient boosting
support vector machine
logistic regression
nested cross-validation
predictive model
url https://www.frontiersin.org/articles/10.3389/fped.2020.570834/full
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