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Differentiation between multiple sclerosis and neuromyelitis optic spectrum disorders with multilevel fMRI features:
Xiao Liang1,2, Qingwen Zeng3, Yanyan Zhu1,2
1Department of Radiology, The First Affiliated Hospital, Jiangxi Medical College, Nanchang University, Nanchang, 330006, Jiangxi, China.
Scientific Reports
|January 14, 2025
Summary
Multilevel functional MRI metrics effectively distinguish multiple sclerosis (MS) from neuromyelitis optic spectrum disorders (NMOSD). Combining resting-state functional connectivity (RSFC), ALFF, and ReHo offers superior diagnostic accuracy over individual features.
Area of Science:
- Neuroimaging
- Machine Learning
- Neurology
Background:
- Conventional statistical analysis of resting-state functional MRI (rs-fMRI) shows limitations in differentiating multiple sclerosis (MS) and neuromyelitis optic spectrum disorders (NMOSD).
- Improved diagnostic tools are crucial for accurate patient management in these neurological conditions.
Purpose of the Study:
- To develop and evaluate machine learning models for distinguishing MS from NMOSD using multilevel rs-fMRI metrics.
- To assess the added value of gray matter volume (GMV) data in classification.
Main Methods:
- Extracted multilevel functional metrics (RSFC, ALFF, ReHo) from 116 brain regions using the anatomical automatic labeling atlas.
- Developed and compared Support Vector Machine (SVM) and Logistic Regression (LR) classifiers integrating these features.
- Evaluated model performance on independent testing cohorts.
Main Results:
- Integrated models combining RSFC, ALFF, and ReHo achieved higher classification performance (SVM AUC=0.857, LR AUC=0.929) than models using individual features.
- Inclusion of GMV data did not significantly enhance classification accuracy.
- Optimal performance was consistent across different brain templates.
Conclusions:
- Multilevel rs-fMRI features (RSFC, ALFF, ReHo) provide a robust and effective method for differentiating MS and NMOSD patients.
- This approach offers a promising avenue for improving diagnostic efficacy in neuroimmunological disorders.

