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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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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
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author Li, Yan
Ge, Zuhao
Zhang, Zhiyan
Shen, Zhiwei
Wang, Yukai
Zhou, Teng
Wu, Renhua
author_facet Li, Yan
Ge, Zuhao
Zhang, Zhiyan
Shen, Zhiwei
Wang, Yukai
Zhou, Teng
Wu, Renhua
author_sort Li, Yan
collection PubMed
description 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.
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spelling pubmed-77041822020-12-08 Broad Learning Enhanced (1)H-MRS for Early Diagnosis of Neuropsychiatric Systemic Lupus Erythematosus Li, Yan Ge, Zuhao Zhang, Zhiyan Shen, Zhiwei Wang, Yukai Zhou, Teng Wu, Renhua Comput Math Methods Med Research Article 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. Hindawi 2020-11-22 /pmc/articles/PMC7704182/ /pubmed/33299467 http://dx.doi.org/10.1155/2020/8874521 Text en Copyright © 2020 Yan Li et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Li, Yan
Ge, Zuhao
Zhang, Zhiyan
Shen, Zhiwei
Wang, Yukai
Zhou, Teng
Wu, Renhua
Broad Learning Enhanced (1)H-MRS for Early Diagnosis of Neuropsychiatric Systemic Lupus Erythematosus
title Broad Learning Enhanced (1)H-MRS for Early Diagnosis of Neuropsychiatric Systemic Lupus Erythematosus
title_full Broad Learning Enhanced (1)H-MRS for Early Diagnosis of Neuropsychiatric Systemic Lupus Erythematosus
title_fullStr Broad Learning Enhanced (1)H-MRS for Early Diagnosis of Neuropsychiatric Systemic Lupus Erythematosus
title_full_unstemmed Broad Learning Enhanced (1)H-MRS for Early Diagnosis of Neuropsychiatric Systemic Lupus Erythematosus
title_short Broad Learning Enhanced (1)H-MRS for Early Diagnosis of Neuropsychiatric Systemic Lupus Erythematosus
title_sort broad learning enhanced (1)h-mrs for early diagnosis of neuropsychiatric systemic lupus erythematosus
topic Research Article
url 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
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