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Intensity standardization of MRI prior to radiomic feature extraction for artificial intelligence research in glioma—a systematic review

OBJECTIVES: Radiomics is a promising avenue in non-invasive characterisation of diffuse glioma. Clinical translation is hampered by lack of reproducibility across centres and difficulty in standardising image intensity in MRI datasets. The study aim was to perform a systematic review of different me...

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Autores principales: Fatania, Kavi, Mohamud, Farah, Clark, Anna, Nix, Michael, Short, Susan C., O’Connor, James, Scarsbrook, Andrew F., Currie, Stuart
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9474349/
https://www.ncbi.nlm.nih.gov/pubmed/35486171
http://dx.doi.org/10.1007/s00330-022-08807-2
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author Fatania, Kavi
Mohamud, Farah
Clark, Anna
Nix, Michael
Short, Susan C.
O’Connor, James
Scarsbrook, Andrew F.
Currie, Stuart
author_facet Fatania, Kavi
Mohamud, Farah
Clark, Anna
Nix, Michael
Short, Susan C.
O’Connor, James
Scarsbrook, Andrew F.
Currie, Stuart
author_sort Fatania, Kavi
collection PubMed
description OBJECTIVES: Radiomics is a promising avenue in non-invasive characterisation of diffuse glioma. Clinical translation is hampered by lack of reproducibility across centres and difficulty in standardising image intensity in MRI datasets. The study aim was to perform a systematic review of different methods of MRI intensity standardisation prior to radiomic feature extraction. METHODS: MEDLINE, EMBASE, and SCOPUS were searched for articles meeting the following eligibility criteria: MRI radiomic studies where one method of intensity normalisation was compared with another or no normalisation, and original research concerning patients diagnosed with diffuse gliomas. Using PRISMA criteria, data were extracted from short-listed studies including number of patients, MRI sequences, validation status, radiomics software, method of segmentation, and intensity standardisation. QUADAS-2 was used for quality appraisal. RESULTS: After duplicate removal, 741 results were returned from database and reference searches and, from these, 12 papers were eligible. Due to a lack of common pre-processing and different analyses, a narrative synthesis was sought. Three different intensity standardisation techniques have been studied: histogram matching (5/12), limiting or rescaling signal intensity (8/12), and deep learning (1/12)—only two papers compared different methods. From these studies, histogram matching produced the more reliable features compared to other methods of altering MRI signal intensity. CONCLUSION: Multiple methods of intensity standardisation have been described in the literature without clear consensus. Further research that directly compares different methods of intensity standardisation on glioma MRI datasets is required. KEY POINTS: • Intensity standardisation is a key pre-processing step in the development of robust radiomic signatures to evaluate diffuse glioma. • A minority of studies compared the impact of two or more methods. • Further research is required to directly compare multiple methods of MRI intensity standardisation on glioma datasets. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00330-022-08807-2.
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spelling pubmed-94743492022-09-16 Intensity standardization of MRI prior to radiomic feature extraction for artificial intelligence research in glioma—a systematic review Fatania, Kavi Mohamud, Farah Clark, Anna Nix, Michael Short, Susan C. O’Connor, James Scarsbrook, Andrew F. Currie, Stuart Eur Radiol Neuro OBJECTIVES: Radiomics is a promising avenue in non-invasive characterisation of diffuse glioma. Clinical translation is hampered by lack of reproducibility across centres and difficulty in standardising image intensity in MRI datasets. The study aim was to perform a systematic review of different methods of MRI intensity standardisation prior to radiomic feature extraction. METHODS: MEDLINE, EMBASE, and SCOPUS were searched for articles meeting the following eligibility criteria: MRI radiomic studies where one method of intensity normalisation was compared with another or no normalisation, and original research concerning patients diagnosed with diffuse gliomas. Using PRISMA criteria, data were extracted from short-listed studies including number of patients, MRI sequences, validation status, radiomics software, method of segmentation, and intensity standardisation. QUADAS-2 was used for quality appraisal. RESULTS: After duplicate removal, 741 results were returned from database and reference searches and, from these, 12 papers were eligible. Due to a lack of common pre-processing and different analyses, a narrative synthesis was sought. Three different intensity standardisation techniques have been studied: histogram matching (5/12), limiting or rescaling signal intensity (8/12), and deep learning (1/12)—only two papers compared different methods. From these studies, histogram matching produced the more reliable features compared to other methods of altering MRI signal intensity. CONCLUSION: Multiple methods of intensity standardisation have been described in the literature without clear consensus. Further research that directly compares different methods of intensity standardisation on glioma MRI datasets is required. KEY POINTS: • Intensity standardisation is a key pre-processing step in the development of robust radiomic signatures to evaluate diffuse glioma. • A minority of studies compared the impact of two or more methods. • Further research is required to directly compare multiple methods of MRI intensity standardisation on glioma datasets. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00330-022-08807-2. Springer Berlin Heidelberg 2022-04-29 2022 /pmc/articles/PMC9474349/ /pubmed/35486171 http://dx.doi.org/10.1007/s00330-022-08807-2 Text en © The Author(s) 2022 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 Neuro
Fatania, Kavi
Mohamud, Farah
Clark, Anna
Nix, Michael
Short, Susan C.
O’Connor, James
Scarsbrook, Andrew F.
Currie, Stuart
Intensity standardization of MRI prior to radiomic feature extraction for artificial intelligence research in glioma—a systematic review
title Intensity standardization of MRI prior to radiomic feature extraction for artificial intelligence research in glioma—a systematic review
title_full Intensity standardization of MRI prior to radiomic feature extraction for artificial intelligence research in glioma—a systematic review
title_fullStr Intensity standardization of MRI prior to radiomic feature extraction for artificial intelligence research in glioma—a systematic review
title_full_unstemmed Intensity standardization of MRI prior to radiomic feature extraction for artificial intelligence research in glioma—a systematic review
title_short Intensity standardization of MRI prior to radiomic feature extraction for artificial intelligence research in glioma—a systematic review
title_sort intensity standardization of mri prior to radiomic feature extraction for artificial intelligence research in glioma—a systematic review
topic Neuro
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9474349/
https://www.ncbi.nlm.nih.gov/pubmed/35486171
http://dx.doi.org/10.1007/s00330-022-08807-2
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