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Differentiation of MOGAD in ADEM-like presentation children based on FLAIR MRI features
Shaonong Wei1, Lu Xu2, Deyang Zhou1
1Machine Learning and I-health International Cooperation Base of Zhejiang Province, Hangzhou Dianzi University, 310018, China; HDU-ITMO Joint Institute, Hangzhou Dianzi University, Zhejiang 310018, China.
Objective:
The differences in magnetic resonance imaging (MRI) between children with classic acute disseminated encephalomyelitis (ADEM) and myelinal oligodendrocyte glycoprotein antibody associated disease (MOGAD) with ADEM-like presentation are controversial. The purpose of this study was to investigate whether the radiological characteristics of the MRI-FLAIR sequence can predict MOGAD in children with ADEM-like presentation and to further explore its imaging differences.
Methods:
We extracted 1041 radiomics features from MRI-FLAIR lesions. Then we used the redundancy analysis (Spearman correlation coefficient), significance test (student test or Mann-Whitney U test), least absolute contraction and selection operator (LASSO) to select potential predictors from the feature groups. The selected potential predictors and MOG antibody test results were used to fit the machine learning model for classification. Combined with feature selection and machine learning classifiers, the optimal model for each subgroup was derived. The resulting models have been evaluated using the receiver operator characteristic curve (ROC) at the lesion level and the model performance was evaluated at the case level using decision curve analysis.
Results:
We retrospectively reviewed and re-diagnosed 70 ADEM-like presentation cases in our center from April 2015 to January 2020. Including 49 cases with classic ADEM and 21 cases with MOGAD. 30(43%) were female, with a median age of 5.3 years. On the four subgroups by age and gender, the area under the curve (AUC) of the optimal models were 89%, 90%, 98%, and 99%, and the MOGAD detection rates (Specificity) were 83%, 83%, 92%, and 75%, respectively.
Conclusions:
The machine learning model trained on radiomics features of MR-FLAIR images can effectively predict patients' MOGAD. This study provides a fast, objective, and quantifiable method for MOGAD diagnosis.
Insights
Machine learning accurately predicts MOGAD in children presenting with ADEM-like symptoms using MRI-FLAIR radiomics. This offers a rapid, objective diagnostic tool for myelinal oligodendrocyte glycoprotein antibody-associated disease.
Area of Science:
- Neurology
- Radiology
- Artificial Intelligence
Background:
- Distinguishing acute disseminated encephalomyelitis (ADEM) from myelinal oligodendrocyte glycoprotein antibody-associated disease (MOGAD) in children is challenging.
- Magnetic resonance imaging (MRI) features, particularly the FLAIR sequence, are crucial for diagnosis but can be similar in ADEM-like presentations.
Purpose of the Study:
- To determine if MRI-FLAIR radiomics can predict MOGAD in pediatric patients with ADEM-like presentations.
- To identify distinct imaging differences between classic ADEM and MOGAD using radiomic features.
Main Methods:
- Extracted 1041 radiomics features from MRI-FLAIR lesions in 70 pediatric cases (49 ADEM, 21 MOGAD).
- Utilized redundancy analysis, significance testing, and LASSO for feature selection.
- Developed and evaluated machine learning classification models using selected features and MOG antibody test results.
Main Results:
- Machine learning models achieved high diagnostic performance, with Area Under the Curve (AUC) ranging from 89% to 99% across subgroups.
- MOGAD detection rates (specificity) varied from 75% to 92% depending on the subgroup.
- The models effectively differentiated MOGAD from ADEM in the pediatric cohort.
Conclusions:
- Radiomics analysis of MRI-FLAIR images, combined with machine learning, is a powerful tool for predicting MOGAD in children with ADEM-like presentations.
- This approach offers a fast, objective, and quantifiable method for improving MOGAD diagnosis.
- The findings support the use of AI-driven radiomics in differentiating neuroinflammatory conditions in pediatric neurology.
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