Cargando…
A magnetic resonance imaging based radiomics model to predict mitosis cycles in intracranial meningioma
The aim of this study was to develop a magnetic resonance imaging (MRI) based radiomics model to predict mitosis cycles in intracranial meningioma grading prior to surgery. Preoperative contrast-enhanced T1-weighted (T1CE) cerebral MRI data of 167 meningioma patients between 2015 and 2020 were obtai...
Autores principales: | , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9849352/ https://www.ncbi.nlm.nih.gov/pubmed/36653482 http://dx.doi.org/10.1038/s41598-023-28089-y |
_version_ | 1784871940941414400 |
---|---|
author | Krähling, Hermann Musigmann, Manfred Akkurt, Burak Han Sartoretti, Thomas Sartoretti, Elisabeth Henssen, Dylan J. H. A. Stummer, Walter Heindel, Walter Brokinkel, Benjamin Mannil, Manoj |
author_facet | Krähling, Hermann Musigmann, Manfred Akkurt, Burak Han Sartoretti, Thomas Sartoretti, Elisabeth Henssen, Dylan J. H. A. Stummer, Walter Heindel, Walter Brokinkel, Benjamin Mannil, Manoj |
author_sort | Krähling, Hermann |
collection | PubMed |
description | The aim of this study was to develop a magnetic resonance imaging (MRI) based radiomics model to predict mitosis cycles in intracranial meningioma grading prior to surgery. Preoperative contrast-enhanced T1-weighted (T1CE) cerebral MRI data of 167 meningioma patients between 2015 and 2020 were obtained, preprocessed and segmented using the 3D Slicer software and the PyRadiomics plugin. In total 145 radiomics features of the T1CE MRI images were computed. The criterion on the basis of which the feature selection was made is whether the number of mitoses per 10 high power field (HPF) is greater than or equal to zero. Our analyses show that machine learning algorithms can be used to make accurate predictions about whether the number of mitoses per 10 HPF is greater than or equal to zero. We obtained our best model using Ridge regression for feature pre-selection, followed by stepwise logistic regression for final model construction. Using independent test data, this model resulted in an AUC (Area under the Curve) of 0.8523, an accuracy of 0.7941, a sensitivity of 0.8182, a specificity of 0.7500 and a Cohen’s Kappa of 0.5576. We analyzed the performance of this model as a function of the number of mitoses per 10 HPF. The model performs well for cases with zero mitoses as well as for cases with more than one mitosis per 10 HPF. The worst model performance (accuracy = 0.6250) is obtained for cases with one mitosis per 10 HPF. Our results show that MRI-based radiomics may be a promising approach to predict the mitosis cycles in intracranial meningioma prior to surgery. Specifically, our approach may offer a non-invasive means of detecting the early stages of a malignant process in meningiomas prior to the onset of clinical symptoms. |
format | Online Article Text |
id | pubmed-9849352 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-98493522023-01-20 A magnetic resonance imaging based radiomics model to predict mitosis cycles in intracranial meningioma Krähling, Hermann Musigmann, Manfred Akkurt, Burak Han Sartoretti, Thomas Sartoretti, Elisabeth Henssen, Dylan J. H. A. Stummer, Walter Heindel, Walter Brokinkel, Benjamin Mannil, Manoj Sci Rep Article The aim of this study was to develop a magnetic resonance imaging (MRI) based radiomics model to predict mitosis cycles in intracranial meningioma grading prior to surgery. Preoperative contrast-enhanced T1-weighted (T1CE) cerebral MRI data of 167 meningioma patients between 2015 and 2020 were obtained, preprocessed and segmented using the 3D Slicer software and the PyRadiomics plugin. In total 145 radiomics features of the T1CE MRI images were computed. The criterion on the basis of which the feature selection was made is whether the number of mitoses per 10 high power field (HPF) is greater than or equal to zero. Our analyses show that machine learning algorithms can be used to make accurate predictions about whether the number of mitoses per 10 HPF is greater than or equal to zero. We obtained our best model using Ridge regression for feature pre-selection, followed by stepwise logistic regression for final model construction. Using independent test data, this model resulted in an AUC (Area under the Curve) of 0.8523, an accuracy of 0.7941, a sensitivity of 0.8182, a specificity of 0.7500 and a Cohen’s Kappa of 0.5576. We analyzed the performance of this model as a function of the number of mitoses per 10 HPF. The model performs well for cases with zero mitoses as well as for cases with more than one mitosis per 10 HPF. The worst model performance (accuracy = 0.6250) is obtained for cases with one mitosis per 10 HPF. Our results show that MRI-based radiomics may be a promising approach to predict the mitosis cycles in intracranial meningioma prior to surgery. Specifically, our approach may offer a non-invasive means of detecting the early stages of a malignant process in meningiomas prior to the onset of clinical symptoms. Nature Publishing Group UK 2023-01-18 /pmc/articles/PMC9849352/ /pubmed/36653482 http://dx.doi.org/10.1038/s41598-023-28089-y Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/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 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/) . |
spellingShingle | Article Krähling, Hermann Musigmann, Manfred Akkurt, Burak Han Sartoretti, Thomas Sartoretti, Elisabeth Henssen, Dylan J. H. A. Stummer, Walter Heindel, Walter Brokinkel, Benjamin Mannil, Manoj A magnetic resonance imaging based radiomics model to predict mitosis cycles in intracranial meningioma |
title | A magnetic resonance imaging based radiomics model to predict mitosis cycles in intracranial meningioma |
title_full | A magnetic resonance imaging based radiomics model to predict mitosis cycles in intracranial meningioma |
title_fullStr | A magnetic resonance imaging based radiomics model to predict mitosis cycles in intracranial meningioma |
title_full_unstemmed | A magnetic resonance imaging based radiomics model to predict mitosis cycles in intracranial meningioma |
title_short | A magnetic resonance imaging based radiomics model to predict mitosis cycles in intracranial meningioma |
title_sort | magnetic resonance imaging based radiomics model to predict mitosis cycles in intracranial meningioma |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9849352/ https://www.ncbi.nlm.nih.gov/pubmed/36653482 http://dx.doi.org/10.1038/s41598-023-28089-y |
work_keys_str_mv | AT krahlinghermann amagneticresonanceimagingbasedradiomicsmodeltopredictmitosiscyclesinintracranialmeningioma AT musigmannmanfred amagneticresonanceimagingbasedradiomicsmodeltopredictmitosiscyclesinintracranialmeningioma AT akkurtburakhan amagneticresonanceimagingbasedradiomicsmodeltopredictmitosiscyclesinintracranialmeningioma AT sartorettithomas amagneticresonanceimagingbasedradiomicsmodeltopredictmitosiscyclesinintracranialmeningioma AT sartorettielisabeth amagneticresonanceimagingbasedradiomicsmodeltopredictmitosiscyclesinintracranialmeningioma AT henssendylanjha amagneticresonanceimagingbasedradiomicsmodeltopredictmitosiscyclesinintracranialmeningioma AT stummerwalter amagneticresonanceimagingbasedradiomicsmodeltopredictmitosiscyclesinintracranialmeningioma AT heindelwalter amagneticresonanceimagingbasedradiomicsmodeltopredictmitosiscyclesinintracranialmeningioma AT brokinkelbenjamin amagneticresonanceimagingbasedradiomicsmodeltopredictmitosiscyclesinintracranialmeningioma AT mannilmanoj amagneticresonanceimagingbasedradiomicsmodeltopredictmitosiscyclesinintracranialmeningioma AT krahlinghermann magneticresonanceimagingbasedradiomicsmodeltopredictmitosiscyclesinintracranialmeningioma AT musigmannmanfred magneticresonanceimagingbasedradiomicsmodeltopredictmitosiscyclesinintracranialmeningioma AT akkurtburakhan magneticresonanceimagingbasedradiomicsmodeltopredictmitosiscyclesinintracranialmeningioma AT sartorettithomas magneticresonanceimagingbasedradiomicsmodeltopredictmitosiscyclesinintracranialmeningioma AT sartorettielisabeth magneticresonanceimagingbasedradiomicsmodeltopredictmitosiscyclesinintracranialmeningioma AT henssendylanjha magneticresonanceimagingbasedradiomicsmodeltopredictmitosiscyclesinintracranialmeningioma AT stummerwalter magneticresonanceimagingbasedradiomicsmodeltopredictmitosiscyclesinintracranialmeningioma AT heindelwalter magneticresonanceimagingbasedradiomicsmodeltopredictmitosiscyclesinintracranialmeningioma AT brokinkelbenjamin magneticresonanceimagingbasedradiomicsmodeltopredictmitosiscyclesinintracranialmeningioma AT mannilmanoj magneticresonanceimagingbasedradiomicsmodeltopredictmitosiscyclesinintracranialmeningioma |