Abstract
Objective
To develop a discrimination pipeline concerning both radiomics and spatial distribution features of brain lesions for discrimination of multiple sclerosis (MS), aquaporin-4-IgG-seropositive neuromyelitis optica spectrum disorder (NMOSD), and myelin-oligodendrocyte-glycoprotein-IgG-associated disorder (MOGAD).
Methods
Hyperintensity T2 lesions were delineated in 212 brain MRI scans of MS (n = 63), NMOSD (n = 87), and MOGAD (n = 45) patients. To avoid the effect of fixed training/test dataset sampling when developing machine learning models, patients were allocated into 4 sub-groups for cross-validation. For each scan, 351 radiomics and 27 spatial distribution features were extracted. Three models, i.e., multi-lesion radiomics, spatial distribution, and joint models, were constructed using random forest and logistic regression algorithms for differentiating: MS from the others (MS models) and MOGAD from NMOSD (MOG-NMO models), respectively. Then, the joint models were combined with demographic characteristics (i.e., age and sex) to create MS and MOG-NMO discriminators, respectively, based on which a three-disease discrimination pipeline was generated and compared with radiologists.
Results
For classification of both MS-others and MOG-NMO, the joint models performed better than radiomics or spatial distribution model solely. The MS discriminator achieved AUC = 0.909 ± 0.027 and bias-corrected C-index = 0.909 ± 0.027, and the MOG-NMO discriminator achieved AUC = 0.880 ± 0.064 and bias-corrected C-index = 0.883 ± 0.068. The three-disease discrimination pipeline differentiated MS, NMOSD, and MOGAD patients with 75.0% accuracy, prominently outperforming the three radiologists (47.6%, 56.6%, and 66.0%).
Conclusions
The proposed pipeline integrating multi-lesion radiomics and spatial distribution features could effectively differentiate MS, NMOSD, and MOGAD.
Clinical relevance statement
The discrimination pipeline merging both radiomics and spatial distribution features of brain lesions may facilitate the differential diagnoses of multiple sclerosis, neuromyelitis optica spectrum disorder, and myelin-oligodendrocyte-glycoprotein-IgG-associated disorder.
Key Points
• Our study introduces an approach by combining radiomics and spatial distribution models.
• The joint model exhibited superior performance in distinguishing multiple sclerosis from aquaporin-4-IgG-seropositive neuromyelitis optica spectrum disorder and myelin-oligodendrocyte-glycoprotein-IgG-associated disorder as well as discriminating the latter two diseases.
• The three-disease discrimination pipeline showcased remarkable accuracy, surpassing the performance of experienced radiologists, highlighting its potential as a valuable diagnostic tool.
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Abbreviations
- AQP4-IgG:
-
Aquaporin-4-immunoglobulin-G
- IBSI:
-
Imaging biomarker standardization initiative
- MOGAD:
-
Myelin-oligodendrocyte-glycoprotein-IgG-associated disorder
- MS:
-
Multiple sclerosis
- NMOSD:
-
Neuromyelitis optica spectrum disorder
- RIL:
-
The Radiomics Index for Lesion
- RIS:
-
The Radiomics Index for Scan
- SDI:
-
The Spatial Distribution Index
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Funding
This work has received funding from the National Natural Science Foundation of China (82102132, 81771296, 82171341, 82102016, 82202122, 8237071280), the Science and Technology Commission of Shanghai Municipality (20S31904300, 22TS1400900, 23S31904100, 22ZR1409500), and the Greater Bay Area Institute of Precision Medicine (Guangzhou) (KCH2310094).
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The scientific guarantor of this publication is Daoying Geng.
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One of the authors has significant statistical expertise.
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Written informed consent was obtained from all subjects (patients) in this study.
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Approval was obtained from Huashan Hospital Institutional Review Board.
Study subjects or cohorts overlap
Some study subjects or cohorts have been previously reported published in two studies: https://doi.org/10.1007/s00330-019-06506-z, and https://doi.org/10.1007/s00330-022-08653-2.
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• retrospective
• cross sectional study
• performed at one institution
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Luo, X., Li, H., Xia, W. et al. Joint radiomics and spatial distribution model for MRI-based discrimination of multiple sclerosis, neuromyelitis optica spectrum disorder, and myelin-oligodendrocyte-glycoprotein-IgG-associated disorder. Eur Radiol (2023). https://doi.org/10.1007/s00330-023-10529-y
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DOI: https://doi.org/10.1007/s00330-023-10529-y