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Broad Learning Enhanced (1)H-MRS for Early Diagnosis of Neuropsychiatric Systemic Lupus Erythematosus

In this paper, we explore the potential of using the multivoxel proton magnetic resonance spectroscopy ((1)H-MRS) to diagnose neuropsychiatric systemic lupus erythematosus (NPSLE) with the assistance of a support vector machine broad learning system (BL-SVM). We retrospectively analysed 23 confirmed...

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Detalles Bibliográficos
Autores principales: Li, Yan, Ge, Zuhao, Zhang, Zhiyan, Shen, Zhiwei, Wang, Yukai, Zhou, Teng, Wu, Renhua
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7704182/
https://www.ncbi.nlm.nih.gov/pubmed/33299467
http://dx.doi.org/10.1155/2020/8874521
Descripción
Sumario:In this paper, we explore the potential of using the multivoxel proton magnetic resonance spectroscopy ((1)H-MRS) to diagnose neuropsychiatric systemic lupus erythematosus (NPSLE) with the assistance of a support vector machine broad learning system (BL-SVM). We retrospectively analysed 23 confirmed patients and 16 healthy controls, who underwent a 3.0 T magnetic resonance imaging (MRI) sequence with multivoxel (1)H-MRS in our hospitals. One hundred and seventeen metabolic features were extracted from the multivoxel (1)H-MRS image. Thirty-three metabolic features selected by the Mann-Whitney U test were considered to have a statistically significant difference (p < 0.05). However, the best accuracy achieved by conventional statistical methods using these 33 metabolic features was only 77%. We turned to develop a support vector machine broad learning system (BL-SVM) to quantitatively analyse the metabolic features from (1)H-MRS. Although not all the individual features manifested statistics significantly, the BL-SVM could still learn to distinguish the NPSLE from the healthy controls. The area under the receiver operating characteristic curve (AUC), the sensitivity, and the specificity of our BL-SVM in predicting NPSLE were 95%, 95.8%, and 93%, respectively, by 3-fold cross-validation. We consequently conclude that the proposed system effectively and efficiently working on limited and noisy samples may brighten a noinvasive in vivo instrument for early diagnosis of NPSLE.