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Assessing treatment switch among patients with multiple sclerosis: A machine learning approach

BACKGROUND: Patients with multiple sclerosis (MS) frequently switch their Disease-Modifying Agents (DMA) for effectiveness and safety concerns. This study aimed to develop and compare the random forest (RF) machine learning (ML) model with the logistic regression (LR) model for predicting DMA switch...

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Autores principales: Li, Jieni, Huang, Yinan, Hutton, George J., Aparasu, Rajender R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10405092/
https://www.ncbi.nlm.nih.gov/pubmed/37554927
http://dx.doi.org/10.1016/j.rcsop.2023.100307
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author Li, Jieni
Huang, Yinan
Hutton, George J.
Aparasu, Rajender R.
author_facet Li, Jieni
Huang, Yinan
Hutton, George J.
Aparasu, Rajender R.
author_sort Li, Jieni
collection PubMed
description BACKGROUND: Patients with multiple sclerosis (MS) frequently switch their Disease-Modifying Agents (DMA) for effectiveness and safety concerns. This study aimed to develop and compare the random forest (RF) machine learning (ML) model with the logistic regression (LR) model for predicting DMA switching among MS patients. METHODS: This retrospective longitudinal study used the TriNetX data from a federated electronic medical records (EMR) network. Between September 2010 and May 2017, adults (aged ≥18) MS patients with ≥1 DMA prescription were identified, and the earliest DMA date was assigned as the index date. Patients prescribed any DMAs different from their index DMAs were considered as treatment switch. . The RF and LR models were built with 72 baseline characteristics and trained with 70% of the randomly split data after up-sampling. Area Under the Curves (AUC), accuracy, recall, G-measure, and F-1 score were used to evaluate the model performance. RESULTS: In this study, 7258 MS patients with ≥1 DMA were identified. Within two years, 16% of MS patients switched to a different DMA. The RF model obtained significantly better discrimination than the LR model (AUC = 0.65 vs. 0.63, p < 0.0001); however, the RF model had a similar predictive performance to the LR model with respect to F- and G-measures (RF: 72% and 73% vs. LR: 72% and 73%, respectively). The most influential features identified from the RF model were age, type of index medication, and year of index. CONCLUSIONS: Compared to the LR model, RF performed better in predicting DMA switch in MS patients based on AUC measures; however, judged by F- and G-measures, the RF model performed similarly to LR. Further research is needed to understand the role of ML techniques in predicting treatment outcomes for the decision-making process to achieve optimal treatment goals.
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spelling pubmed-104050922023-08-08 Assessing treatment switch among patients with multiple sclerosis: A machine learning approach Li, Jieni Huang, Yinan Hutton, George J. Aparasu, Rajender R. Explor Res Clin Soc Pharm Article BACKGROUND: Patients with multiple sclerosis (MS) frequently switch their Disease-Modifying Agents (DMA) for effectiveness and safety concerns. This study aimed to develop and compare the random forest (RF) machine learning (ML) model with the logistic regression (LR) model for predicting DMA switching among MS patients. METHODS: This retrospective longitudinal study used the TriNetX data from a federated electronic medical records (EMR) network. Between September 2010 and May 2017, adults (aged ≥18) MS patients with ≥1 DMA prescription were identified, and the earliest DMA date was assigned as the index date. Patients prescribed any DMAs different from their index DMAs were considered as treatment switch. . The RF and LR models were built with 72 baseline characteristics and trained with 70% of the randomly split data after up-sampling. Area Under the Curves (AUC), accuracy, recall, G-measure, and F-1 score were used to evaluate the model performance. RESULTS: In this study, 7258 MS patients with ≥1 DMA were identified. Within two years, 16% of MS patients switched to a different DMA. The RF model obtained significantly better discrimination than the LR model (AUC = 0.65 vs. 0.63, p < 0.0001); however, the RF model had a similar predictive performance to the LR model with respect to F- and G-measures (RF: 72% and 73% vs. LR: 72% and 73%, respectively). The most influential features identified from the RF model were age, type of index medication, and year of index. CONCLUSIONS: Compared to the LR model, RF performed better in predicting DMA switch in MS patients based on AUC measures; however, judged by F- and G-measures, the RF model performed similarly to LR. Further research is needed to understand the role of ML techniques in predicting treatment outcomes for the decision-making process to achieve optimal treatment goals. Elsevier 2023-07-10 /pmc/articles/PMC10405092/ /pubmed/37554927 http://dx.doi.org/10.1016/j.rcsop.2023.100307 Text en © 2023 The Author(s) https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Li, Jieni
Huang, Yinan
Hutton, George J.
Aparasu, Rajender R.
Assessing treatment switch among patients with multiple sclerosis: A machine learning approach
title Assessing treatment switch among patients with multiple sclerosis: A machine learning approach
title_full Assessing treatment switch among patients with multiple sclerosis: A machine learning approach
title_fullStr Assessing treatment switch among patients with multiple sclerosis: A machine learning approach
title_full_unstemmed Assessing treatment switch among patients with multiple sclerosis: A machine learning approach
title_short Assessing treatment switch among patients with multiple sclerosis: A machine learning approach
title_sort assessing treatment switch among patients with multiple sclerosis: a machine learning approach
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10405092/
https://www.ncbi.nlm.nih.gov/pubmed/37554927
http://dx.doi.org/10.1016/j.rcsop.2023.100307
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