Cargando…
Multi-parametric MRI phenotype with trustworthy machine learning for differentiating CNS demyelinating diseases
BACKGROUND: Misdiagnosis of multiple sclerosis (MS) and neuromyelitis optica (NMO) may delay the treatment, resulting in poor prognosis. However, the precise identification of these two diseases is still challenging in clinical practice. We aimed to evaluate the value of quantitative radiomic featur...
Autores principales: | , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8419989/ https://www.ncbi.nlm.nih.gov/pubmed/34488799 http://dx.doi.org/10.1186/s12967-021-03015-w |
_version_ | 1783748869455085568 |
---|---|
author | Huang, Jing Xin, Bowen Wang, Xiuying Qi, Zhigang Dong, Huiqing Li, Kuncheng Zhou, Yun Lu, Jie |
author_facet | Huang, Jing Xin, Bowen Wang, Xiuying Qi, Zhigang Dong, Huiqing Li, Kuncheng Zhou, Yun Lu, Jie |
author_sort | Huang, Jing |
collection | PubMed |
description | BACKGROUND: Misdiagnosis of multiple sclerosis (MS) and neuromyelitis optica (NMO) may delay the treatment, resulting in poor prognosis. However, the precise identification of these two diseases is still challenging in clinical practice. We aimed to evaluate the value of quantitative radiomic features extracted from the brain white matter lesions for differential diagnosis of MS and NMO. METHODS: We recruited 116 CNS demyelinating patients including 78 MS, and 38 NMO. Three neuroradiologists performed visual differential diagnosis based on brain MRI for comparison purpose. A multi-level scheme was designed to harness the selection of discriminative and stable radiomics features extracted from brain while mater lesions in T1-MPRAGE, T2 sequences and clinical factors. Based on the imaging phenotype composed of the selected radiomic and clinical features, Multi-parametric Multivariate Random Forest (MM-RF) model was constructed and verified with both 10-fold cross-validation and independent testing. Result interpretation was provided to build trust in diagnostic decisions. RESULTS: Eighty-six patients were randomly selected to form the training set while the rest 30 patients for independent testing. On the training set, our MM-RF model achieved accuracy 0.849 and AUC 0.826 in 10-fold cross-validation, which were significantly higher than clinical visual analysis (0.709 and 0.683, p < 0.05). In the independent testing, the MM-RF model achieved AUC 0.902, accuracy 0.871, sensitivity 0.873, specificity 0.869, respectively. Furthermore, age, sex and EDSS were found mildly correlated with the radiomic features (p of all < 0.05). CONCLUSIONS: Multi-parametric radiomic features have potential as practical quantitative imaging biomarkers for differentiating MS from NMO. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12967-021-03015-w. |
format | Online Article Text |
id | pubmed-8419989 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-84199892021-09-09 Multi-parametric MRI phenotype with trustworthy machine learning for differentiating CNS demyelinating diseases Huang, Jing Xin, Bowen Wang, Xiuying Qi, Zhigang Dong, Huiqing Li, Kuncheng Zhou, Yun Lu, Jie J Transl Med Research BACKGROUND: Misdiagnosis of multiple sclerosis (MS) and neuromyelitis optica (NMO) may delay the treatment, resulting in poor prognosis. However, the precise identification of these two diseases is still challenging in clinical practice. We aimed to evaluate the value of quantitative radiomic features extracted from the brain white matter lesions for differential diagnosis of MS and NMO. METHODS: We recruited 116 CNS demyelinating patients including 78 MS, and 38 NMO. Three neuroradiologists performed visual differential diagnosis based on brain MRI for comparison purpose. A multi-level scheme was designed to harness the selection of discriminative and stable radiomics features extracted from brain while mater lesions in T1-MPRAGE, T2 sequences and clinical factors. Based on the imaging phenotype composed of the selected radiomic and clinical features, Multi-parametric Multivariate Random Forest (MM-RF) model was constructed and verified with both 10-fold cross-validation and independent testing. Result interpretation was provided to build trust in diagnostic decisions. RESULTS: Eighty-six patients were randomly selected to form the training set while the rest 30 patients for independent testing. On the training set, our MM-RF model achieved accuracy 0.849 and AUC 0.826 in 10-fold cross-validation, which were significantly higher than clinical visual analysis (0.709 and 0.683, p < 0.05). In the independent testing, the MM-RF model achieved AUC 0.902, accuracy 0.871, sensitivity 0.873, specificity 0.869, respectively. Furthermore, age, sex and EDSS were found mildly correlated with the radiomic features (p of all < 0.05). CONCLUSIONS: Multi-parametric radiomic features have potential as practical quantitative imaging biomarkers for differentiating MS from NMO. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12967-021-03015-w. BioMed Central 2021-09-06 /pmc/articles/PMC8419989/ /pubmed/34488799 http://dx.doi.org/10.1186/s12967-021-03015-w Text en © The Author(s) 2021 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 Huang, Jing Xin, Bowen Wang, Xiuying Qi, Zhigang Dong, Huiqing Li, Kuncheng Zhou, Yun Lu, Jie Multi-parametric MRI phenotype with trustworthy machine learning for differentiating CNS demyelinating diseases |
title | Multi-parametric MRI phenotype with trustworthy machine learning for differentiating CNS demyelinating diseases |
title_full | Multi-parametric MRI phenotype with trustworthy machine learning for differentiating CNS demyelinating diseases |
title_fullStr | Multi-parametric MRI phenotype with trustworthy machine learning for differentiating CNS demyelinating diseases |
title_full_unstemmed | Multi-parametric MRI phenotype with trustworthy machine learning for differentiating CNS demyelinating diseases |
title_short | Multi-parametric MRI phenotype with trustworthy machine learning for differentiating CNS demyelinating diseases |
title_sort | multi-parametric mri phenotype with trustworthy machine learning for differentiating cns demyelinating diseases |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8419989/ https://www.ncbi.nlm.nih.gov/pubmed/34488799 http://dx.doi.org/10.1186/s12967-021-03015-w |
work_keys_str_mv | AT huangjing multiparametricmriphenotypewithtrustworthymachinelearningfordifferentiatingcnsdemyelinatingdiseases AT xinbowen multiparametricmriphenotypewithtrustworthymachinelearningfordifferentiatingcnsdemyelinatingdiseases AT wangxiuying multiparametricmriphenotypewithtrustworthymachinelearningfordifferentiatingcnsdemyelinatingdiseases AT qizhigang multiparametricmriphenotypewithtrustworthymachinelearningfordifferentiatingcnsdemyelinatingdiseases AT donghuiqing multiparametricmriphenotypewithtrustworthymachinelearningfordifferentiatingcnsdemyelinatingdiseases AT likuncheng multiparametricmriphenotypewithtrustworthymachinelearningfordifferentiatingcnsdemyelinatingdiseases AT zhouyun multiparametricmriphenotypewithtrustworthymachinelearningfordifferentiatingcnsdemyelinatingdiseases AT lujie multiparametricmriphenotypewithtrustworthymachinelearningfordifferentiatingcnsdemyelinatingdiseases |