Cargando…
Development of a 32-gene signature using machine learning for accurate prediction of inflammatory bowel disease
Inflammatory bowel disease (IBD) is a chronic inflammatory condition caused by multiple genetic and environmental factors. Numerous genes are implicated in the etiology of IBD, but the diagnosis of IBD is challenging. Here, XGBoost, a machine learning prediction model, has been used to distinguish I...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Nature Singapore
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9813306/ https://www.ncbi.nlm.nih.gov/pubmed/36600111 http://dx.doi.org/10.1186/s13619-022-00143-6 |
_version_ | 1784863896667947008 |
---|---|
author | Yu, Shicheng Zhang, Mengxian Ye, Zhaofeng Wang, Yalong Wang, Xu Chen, Ye-Guang |
author_facet | Yu, Shicheng Zhang, Mengxian Ye, Zhaofeng Wang, Yalong Wang, Xu Chen, Ye-Guang |
author_sort | Yu, Shicheng |
collection | PubMed |
description | Inflammatory bowel disease (IBD) is a chronic inflammatory condition caused by multiple genetic and environmental factors. Numerous genes are implicated in the etiology of IBD, but the diagnosis of IBD is challenging. Here, XGBoost, a machine learning prediction model, has been used to distinguish IBD from healthy cases following elaborative feature selection. Using combined unsupervised clustering analysis and the XGBoost feature selection method, we successfully identified a 32-gene signature that can predict IBD occurrence in new cohorts with 0.8651 accuracy. The signature shows enrichment in neutrophil extracellular trap formation and cytokine signaling in the immune system. The probability threshold of the XGBoost-based classification model can be adjusted to fit personalized lifestyle and health status. Therefore, this study reveals potential IBD-related biomarkers that facilitate an effective personalized diagnosis of IBD. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13619-022-00143-6. |
format | Online Article Text |
id | pubmed-9813306 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Springer Nature Singapore |
record_format | MEDLINE/PubMed |
spelling | pubmed-98133062023-01-17 Development of a 32-gene signature using machine learning for accurate prediction of inflammatory bowel disease Yu, Shicheng Zhang, Mengxian Ye, Zhaofeng Wang, Yalong Wang, Xu Chen, Ye-Guang Cell Regen Research Article Inflammatory bowel disease (IBD) is a chronic inflammatory condition caused by multiple genetic and environmental factors. Numerous genes are implicated in the etiology of IBD, but the diagnosis of IBD is challenging. Here, XGBoost, a machine learning prediction model, has been used to distinguish IBD from healthy cases following elaborative feature selection. Using combined unsupervised clustering analysis and the XGBoost feature selection method, we successfully identified a 32-gene signature that can predict IBD occurrence in new cohorts with 0.8651 accuracy. The signature shows enrichment in neutrophil extracellular trap formation and cytokine signaling in the immune system. The probability threshold of the XGBoost-based classification model can be adjusted to fit personalized lifestyle and health status. Therefore, this study reveals potential IBD-related biomarkers that facilitate an effective personalized diagnosis of IBD. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13619-022-00143-6. Springer Nature Singapore 2023-01-05 /pmc/articles/PMC9813306/ /pubmed/36600111 http://dx.doi.org/10.1186/s13619-022-00143-6 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Article Yu, Shicheng Zhang, Mengxian Ye, Zhaofeng Wang, Yalong Wang, Xu Chen, Ye-Guang Development of a 32-gene signature using machine learning for accurate prediction of inflammatory bowel disease |
title | Development of a 32-gene signature using machine learning for accurate prediction of inflammatory bowel disease |
title_full | Development of a 32-gene signature using machine learning for accurate prediction of inflammatory bowel disease |
title_fullStr | Development of a 32-gene signature using machine learning for accurate prediction of inflammatory bowel disease |
title_full_unstemmed | Development of a 32-gene signature using machine learning for accurate prediction of inflammatory bowel disease |
title_short | Development of a 32-gene signature using machine learning for accurate prediction of inflammatory bowel disease |
title_sort | development of a 32-gene signature using machine learning for accurate prediction of inflammatory bowel disease |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9813306/ https://www.ncbi.nlm.nih.gov/pubmed/36600111 http://dx.doi.org/10.1186/s13619-022-00143-6 |
work_keys_str_mv | AT yushicheng developmentofa32genesignatureusingmachinelearningforaccuratepredictionofinflammatoryboweldisease AT zhangmengxian developmentofa32genesignatureusingmachinelearningforaccuratepredictionofinflammatoryboweldisease AT yezhaofeng developmentofa32genesignatureusingmachinelearningforaccuratepredictionofinflammatoryboweldisease AT wangyalong developmentofa32genesignatureusingmachinelearningforaccuratepredictionofinflammatoryboweldisease AT wangxu developmentofa32genesignatureusingmachinelearningforaccuratepredictionofinflammatoryboweldisease AT chenyeguang developmentofa32genesignatureusingmachinelearningforaccuratepredictionofinflammatoryboweldisease |