4.0 Article

Optimal Integration of Machine Learning for Distinct Classification and Activity State Determination in Multiple Sclerosis and Neuromyelitis Optica

期刊

TECHNOLOGIES
卷 11, 期 5, 页码 -

出版社

MDPI
DOI: 10.3390/technologies11050131

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machine learning; deep learning; medical diagnosis; multiple sclerosis; neuromyelitis optica; feature selection

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In this study, an innovative diagnostic approach for accurately locating multiple sclerosis (MS) and neuromyelitis optica (NMO) using machine learning algorithms applied to MRI scans was developed. The results demonstrated that KNN and SVM algorithms performed superiorly in differentiating between MS and NMO, and classifying active versus inactive states of MS, respectively. This advanced methodology provides clinicians with a highly accurate, efficient tool for diagnosing these diseases and has the potential to streamline treatment processes.
The intricate neuroinflammatory diseases multiple sclerosis (MS) and neuromyelitis optica (NMO) often present similar clinical symptoms, creating challenges in their precise detection via magnetic resonance imaging (MRI). This challenge is further compounded when detecting the active and inactive states of MS. To address this diagnostic problem, we introduce an innovative framework that incorporates state-of-the-art machine learning algorithms applied to features culled from MRI scans by pre-trained deep learning models, VGG-NET and InceptionV3. To develop and test this methodology, we utilized a robust dataset obtained from the King Abdullah University Hospital in Jordan, encompassing cases diagnosed with both MS and NMO. We benchmarked thirteen distinct machine learning algorithms and discovered that support vector machine (SVM) and K-nearest neighbor (KNN) algorithms performed superiorly in our context. Our results demonstrated KNN's exceptional performance in differentiating between MS and NMO, with precision, recall, F1-score, and accuracy values of 0.98, 0.99, 0.99, and 0.99, respectively, using leveraging features extracted from VGG16. In contrast, SVM excelled in classifying active versus inactive states of MS, achieving precision, recall, F1-score, and accuracy values of 0.99, 0.97, 0.98, and 0.98, respectively, using leveraging features extracted from VGG16 and VGG19. Our advanced methodology outshines previous studies, providing clinicians with a highly accurate, efficient tool for diagnosing these diseases. The immediate implication of our research is the potential to streamline treatment processes, thereby delivering timely, appropriate care to patients suffering from these complex diseases.

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