Exploration of machine learning techniques in predicting multiple sclerosis disease course.

OBJECTIVE:To explore the value of machine learning methods for predicting multiple sclerosis disease course. METHODS:1693 CLIMB study patients were classified as increased EDSS≥1.5 (worsening) or not (non-worsening) at up to five years after baseline visit. Support vector machines (SVM) were used to...

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Main Authors: Yijun Zhao, Brian C Healy, Dalia Rotstein, Charles R G Guttmann, Rohit Bakshi, Howard L Weiner, Carla E Brodley, Tanuja Chitnis
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2017-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC5381810?pdf=render
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spelling doaj-69987d0a93b949f684bdc5835115f17f2020-11-24T21:35:36ZengPublic Library of Science (PLoS)PLoS ONE1932-62032017-01-01124e017486610.1371/journal.pone.0174866Exploration of machine learning techniques in predicting multiple sclerosis disease course.Yijun ZhaoBrian C HealyDalia RotsteinCharles R G GuttmannRohit BakshiHoward L WeinerCarla E BrodleyTanuja ChitnisOBJECTIVE:To explore the value of machine learning methods for predicting multiple sclerosis disease course. METHODS:1693 CLIMB study patients were classified as increased EDSS≥1.5 (worsening) or not (non-worsening) at up to five years after baseline visit. Support vector machines (SVM) were used to build the classifier, and compared to logistic regression (LR) using demographic, clinical and MRI data obtained at years one and two to predict EDSS at five years follow-up. RESULTS:Baseline data alone provided little predictive value. Clinical observation for one year improved overall SVM sensitivity to 62% and specificity to 65% in predicting worsening cases. The addition of one year MRI data improved sensitivity to 71% and specificity to 68%. Use of non-uniform misclassification costs in the SVM model, weighting towards increased sensitivity, improved predictions (up to 86%). Sensitivity, specificity, and overall accuracy improved minimally with additional follow-up data. Predictions improved within specific groups defined by baseline EDSS. LR performed more poorly than SVM in most cases. Race, family history of MS, and brain parenchymal fraction, ranked highly as predictors of the non-worsening group. Brain T2 lesion volume ranked highly as predictive of the worsening group. INTERPRETATION:SVM incorporating short-term clinical and brain MRI data, class imbalance corrective measures, and classification costs may be a promising means to predict MS disease course, and for selection of patients suitable for more aggressive treatment regimens.http://europepmc.org/articles/PMC5381810?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Yijun Zhao
Brian C Healy
Dalia Rotstein
Charles R G Guttmann
Rohit Bakshi
Howard L Weiner
Carla E Brodley
Tanuja Chitnis
spellingShingle Yijun Zhao
Brian C Healy
Dalia Rotstein
Charles R G Guttmann
Rohit Bakshi
Howard L Weiner
Carla E Brodley
Tanuja Chitnis
Exploration of machine learning techniques in predicting multiple sclerosis disease course.
PLoS ONE
author_facet Yijun Zhao
Brian C Healy
Dalia Rotstein
Charles R G Guttmann
Rohit Bakshi
Howard L Weiner
Carla E Brodley
Tanuja Chitnis
author_sort Yijun Zhao
title Exploration of machine learning techniques in predicting multiple sclerosis disease course.
title_short Exploration of machine learning techniques in predicting multiple sclerosis disease course.
title_full Exploration of machine learning techniques in predicting multiple sclerosis disease course.
title_fullStr Exploration of machine learning techniques in predicting multiple sclerosis disease course.
title_full_unstemmed Exploration of machine learning techniques in predicting multiple sclerosis disease course.
title_sort exploration of machine learning techniques in predicting multiple sclerosis disease course.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2017-01-01
description OBJECTIVE:To explore the value of machine learning methods for predicting multiple sclerosis disease course. METHODS:1693 CLIMB study patients were classified as increased EDSS≥1.5 (worsening) or not (non-worsening) at up to five years after baseline visit. Support vector machines (SVM) were used to build the classifier, and compared to logistic regression (LR) using demographic, clinical and MRI data obtained at years one and two to predict EDSS at five years follow-up. RESULTS:Baseline data alone provided little predictive value. Clinical observation for one year improved overall SVM sensitivity to 62% and specificity to 65% in predicting worsening cases. The addition of one year MRI data improved sensitivity to 71% and specificity to 68%. Use of non-uniform misclassification costs in the SVM model, weighting towards increased sensitivity, improved predictions (up to 86%). Sensitivity, specificity, and overall accuracy improved minimally with additional follow-up data. Predictions improved within specific groups defined by baseline EDSS. LR performed more poorly than SVM in most cases. Race, family history of MS, and brain parenchymal fraction, ranked highly as predictors of the non-worsening group. Brain T2 lesion volume ranked highly as predictive of the worsening group. INTERPRETATION:SVM incorporating short-term clinical and brain MRI data, class imbalance corrective measures, and classification costs may be a promising means to predict MS disease course, and for selection of patients suitable for more aggressive treatment regimens.
url http://europepmc.org/articles/PMC5381810?pdf=render
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