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In silico clinical trials for pediatric orphan diseases
To date poor treatment options are available for patients with congenital pseudarthrosis of the tibia (CPT), a pediatric orphan disease. In this study we have performed an in silico clinical trial on 200 virtual subjects, generated from a previously established model of murine bone regeneration, to...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5802824/ https://www.ncbi.nlm.nih.gov/pubmed/29410461 http://dx.doi.org/10.1038/s41598-018-20737-y |
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author | Carlier, A. Vasilevich, A. Marechal, M. de Boer, J. Geris, L. |
author_facet | Carlier, A. Vasilevich, A. Marechal, M. de Boer, J. Geris, L. |
author_sort | Carlier, A. |
collection | PubMed |
description | To date poor treatment options are available for patients with congenital pseudarthrosis of the tibia (CPT), a pediatric orphan disease. In this study we have performed an in silico clinical trial on 200 virtual subjects, generated from a previously established model of murine bone regeneration, to tackle the challenges associated with the small, pediatric patient population. Each virtual subject was simulated to receive no treatment and bone morphogenetic protein (BMP) treatment. We have shown that the degree of severity of CPT is significantly reduced with BMP treatment, although the effect is highly subject-specific. Using machine learning techniques we were also able to stratify the virtual subject population in adverse responders, non-responders, responders and asymptomatic. In summary, this study shows the potential of in silico medicine technologies as well as their implications for other orphan diseases. |
format | Online Article Text |
id | pubmed-5802824 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-58028242018-02-14 In silico clinical trials for pediatric orphan diseases Carlier, A. Vasilevich, A. Marechal, M. de Boer, J. Geris, L. Sci Rep Article To date poor treatment options are available for patients with congenital pseudarthrosis of the tibia (CPT), a pediatric orphan disease. In this study we have performed an in silico clinical trial on 200 virtual subjects, generated from a previously established model of murine bone regeneration, to tackle the challenges associated with the small, pediatric patient population. Each virtual subject was simulated to receive no treatment and bone morphogenetic protein (BMP) treatment. We have shown that the degree of severity of CPT is significantly reduced with BMP treatment, although the effect is highly subject-specific. Using machine learning techniques we were also able to stratify the virtual subject population in adverse responders, non-responders, responders and asymptomatic. In summary, this study shows the potential of in silico medicine technologies as well as their implications for other orphan diseases. Nature Publishing Group UK 2018-02-06 /pmc/articles/PMC5802824/ /pubmed/29410461 http://dx.doi.org/10.1038/s41598-018-20737-y Text en © The Author(s) 2018 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 Carlier, A. Vasilevich, A. Marechal, M. de Boer, J. Geris, L. In silico clinical trials for pediatric orphan diseases |
title | In silico clinical trials for pediatric orphan diseases |
title_full | In silico clinical trials for pediatric orphan diseases |
title_fullStr | In silico clinical trials for pediatric orphan diseases |
title_full_unstemmed | In silico clinical trials for pediatric orphan diseases |
title_short | In silico clinical trials for pediatric orphan diseases |
title_sort | in silico clinical trials for pediatric orphan diseases |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5802824/ https://www.ncbi.nlm.nih.gov/pubmed/29410461 http://dx.doi.org/10.1038/s41598-018-20737-y |
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