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Predicting Methylphenidate Response in ADHD Using Machine Learning Approaches

BACKGROUND: There are no objective, biological markers that can robustly predict methylphenidate response in attention deficit hyperactivity disorder. This study aimed to examine whether applying machine learning approaches to pretreatment demographic, clinical questionnaire, environmental, neuropsy...

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Autores principales: Kim, Jae-Won, Sharma, Vinod, Ryan, Neal D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4756719/
https://www.ncbi.nlm.nih.gov/pubmed/25964505
http://dx.doi.org/10.1093/ijnp/pyv052
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author Kim, Jae-Won
Sharma, Vinod
Ryan, Neal D.
author_facet Kim, Jae-Won
Sharma, Vinod
Ryan, Neal D.
author_sort Kim, Jae-Won
collection PubMed
description BACKGROUND: There are no objective, biological markers that can robustly predict methylphenidate response in attention deficit hyperactivity disorder. This study aimed to examine whether applying machine learning approaches to pretreatment demographic, clinical questionnaire, environmental, neuropsychological, neuroimaging, and genetic information can predict therapeutic response following methylphenidate administration. METHODS: The present study included 83 attention deficit hyperactivity disorder youth. At baseline, parents completed the ADHD Rating Scale-IV and Disruptive Behavior Disorder rating scale, and participants undertook the continuous performance test, Stroop color word test, and resting-state functional MRI scans. The dopamine transporter gene, dopamine D4 receptor gene, alpha-2A adrenergic receptor gene (ADRA2A) and norepinephrine transporter gene polymorphisms, and blood lead and urine cotinine levels were also measured. The participants were enrolled in an 8-week, open-label trial of methylphenidate. Four different machine learning algorithms were used for data analysis. RESULTS: Support vector machine classification accuracy was 84.6% (area under receiver operating characteristic curve 0.84) for predicting methylphenidate response. The age, weight, ADRA2A MspI and DraI polymorphisms, lead level, Stroop color word test performance, and oppositional symptoms of Disruptive Behavior Disorder rating scale were identified as the most differentiating subset of features. CONCLUSIONS: Our results provide preliminary support to the translational development of support vector machine as an informative method that can assist in predicting treatment response in attention deficit hyperactivity disorder, though further work is required to provide enhanced levels of classification performance.
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spelling pubmed-47567192016-02-17 Predicting Methylphenidate Response in ADHD Using Machine Learning Approaches Kim, Jae-Won Sharma, Vinod Ryan, Neal D. Int J Neuropsychopharmacol Research Article BACKGROUND: There are no objective, biological markers that can robustly predict methylphenidate response in attention deficit hyperactivity disorder. This study aimed to examine whether applying machine learning approaches to pretreatment demographic, clinical questionnaire, environmental, neuropsychological, neuroimaging, and genetic information can predict therapeutic response following methylphenidate administration. METHODS: The present study included 83 attention deficit hyperactivity disorder youth. At baseline, parents completed the ADHD Rating Scale-IV and Disruptive Behavior Disorder rating scale, and participants undertook the continuous performance test, Stroop color word test, and resting-state functional MRI scans. The dopamine transporter gene, dopamine D4 receptor gene, alpha-2A adrenergic receptor gene (ADRA2A) and norepinephrine transporter gene polymorphisms, and blood lead and urine cotinine levels were also measured. The participants were enrolled in an 8-week, open-label trial of methylphenidate. Four different machine learning algorithms were used for data analysis. RESULTS: Support vector machine classification accuracy was 84.6% (area under receiver operating characteristic curve 0.84) for predicting methylphenidate response. The age, weight, ADRA2A MspI and DraI polymorphisms, lead level, Stroop color word test performance, and oppositional symptoms of Disruptive Behavior Disorder rating scale were identified as the most differentiating subset of features. CONCLUSIONS: Our results provide preliminary support to the translational development of support vector machine as an informative method that can assist in predicting treatment response in attention deficit hyperactivity disorder, though further work is required to provide enhanced levels of classification performance. Oxford University Press 2015-05-11 /pmc/articles/PMC4756719/ /pubmed/25964505 http://dx.doi.org/10.1093/ijnp/pyv052 Text en © The Author 2015. Published by Oxford University Press on behalf of CINP. http://creativecommons.org/licenses/by-nc/4.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Research Article
Kim, Jae-Won
Sharma, Vinod
Ryan, Neal D.
Predicting Methylphenidate Response in ADHD Using Machine Learning Approaches
title Predicting Methylphenidate Response in ADHD Using Machine Learning Approaches
title_full Predicting Methylphenidate Response in ADHD Using Machine Learning Approaches
title_fullStr Predicting Methylphenidate Response in ADHD Using Machine Learning Approaches
title_full_unstemmed Predicting Methylphenidate Response in ADHD Using Machine Learning Approaches
title_short Predicting Methylphenidate Response in ADHD Using Machine Learning Approaches
title_sort predicting methylphenidate response in adhd using machine learning approaches
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4756719/
https://www.ncbi.nlm.nih.gov/pubmed/25964505
http://dx.doi.org/10.1093/ijnp/pyv052
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