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Classification of Paediatric Inflammatory Bowel Disease using Machine Learning
Paediatric inflammatory bowel disease (PIBD), comprising Crohn’s disease (CD), ulcerative colitis (UC) and inflammatory bowel disease unclassified (IBDU) is a complex and multifactorial condition with increasing incidence. An accurate diagnosis of PIBD is necessary for a prompt and effective treatme...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5445076/ https://www.ncbi.nlm.nih.gov/pubmed/28546534 http://dx.doi.org/10.1038/s41598-017-02606-2 |
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author | Mossotto, E. Ashton, J. J. Coelho, T. Beattie, R. M. MacArthur, B. D. Ennis, S. |
author_facet | Mossotto, E. Ashton, J. J. Coelho, T. Beattie, R. M. MacArthur, B. D. Ennis, S. |
author_sort | Mossotto, E. |
collection | PubMed |
description | Paediatric inflammatory bowel disease (PIBD), comprising Crohn’s disease (CD), ulcerative colitis (UC) and inflammatory bowel disease unclassified (IBDU) is a complex and multifactorial condition with increasing incidence. An accurate diagnosis of PIBD is necessary for a prompt and effective treatment. This study utilises machine learning (ML) to classify disease using endoscopic and histological data for 287 children diagnosed with PIBD. Data were used to develop, train, test and validate a ML model to classify disease subtype. Unsupervised models revealed overlap of CD/UC with broad clustering but no clear subtype delineation, whereas hierarchical clustering identified four novel subgroups characterised by differing colonic involvement. Three supervised ML models were developed utilising endoscopic data only, histological only and combined endoscopic/histological data yielding classification accuracy of 71.0%, 76.9% and 82.7% respectively. The optimal combined model was tested on a statistically independent cohort of 48 PIBD patients from the same clinic, accurately classifying 83.3% of patients. This study employs mathematical modelling of endoscopic and histological data to aid diagnostic accuracy. While unsupervised modelling categorises patients into four subgroups, supervised approaches confirm the need of both endoscopic and histological evidence for an accurate diagnosis. Overall, this paper provides a blueprint for ML use with clinical data. |
format | Online Article Text |
id | pubmed-5445076 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-54450762017-05-30 Classification of Paediatric Inflammatory Bowel Disease using Machine Learning Mossotto, E. Ashton, J. J. Coelho, T. Beattie, R. M. MacArthur, B. D. Ennis, S. Sci Rep Article Paediatric inflammatory bowel disease (PIBD), comprising Crohn’s disease (CD), ulcerative colitis (UC) and inflammatory bowel disease unclassified (IBDU) is a complex and multifactorial condition with increasing incidence. An accurate diagnosis of PIBD is necessary for a prompt and effective treatment. This study utilises machine learning (ML) to classify disease using endoscopic and histological data for 287 children diagnosed with PIBD. Data were used to develop, train, test and validate a ML model to classify disease subtype. Unsupervised models revealed overlap of CD/UC with broad clustering but no clear subtype delineation, whereas hierarchical clustering identified four novel subgroups characterised by differing colonic involvement. Three supervised ML models were developed utilising endoscopic data only, histological only and combined endoscopic/histological data yielding classification accuracy of 71.0%, 76.9% and 82.7% respectively. The optimal combined model was tested on a statistically independent cohort of 48 PIBD patients from the same clinic, accurately classifying 83.3% of patients. This study employs mathematical modelling of endoscopic and histological data to aid diagnostic accuracy. While unsupervised modelling categorises patients into four subgroups, supervised approaches confirm the need of both endoscopic and histological evidence for an accurate diagnosis. Overall, this paper provides a blueprint for ML use with clinical data. Nature Publishing Group UK 2017-05-25 /pmc/articles/PMC5445076/ /pubmed/28546534 http://dx.doi.org/10.1038/s41598-017-02606-2 Text en © The Author(s) 2017 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Mossotto, E. Ashton, J. J. Coelho, T. Beattie, R. M. MacArthur, B. D. Ennis, S. Classification of Paediatric Inflammatory Bowel Disease using Machine Learning |
title | Classification of Paediatric Inflammatory Bowel Disease using Machine Learning |
title_full | Classification of Paediatric Inflammatory Bowel Disease using Machine Learning |
title_fullStr | Classification of Paediatric Inflammatory Bowel Disease using Machine Learning |
title_full_unstemmed | Classification of Paediatric Inflammatory Bowel Disease using Machine Learning |
title_short | Classification of Paediatric Inflammatory Bowel Disease using Machine Learning |
title_sort | classification of paediatric inflammatory bowel disease using machine learning |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5445076/ https://www.ncbi.nlm.nih.gov/pubmed/28546534 http://dx.doi.org/10.1038/s41598-017-02606-2 |
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