A multiple-tissue-specific magnetic resonance imaging model for diagnosing Parkinson's disease: a brain radiomics study

Brain radiomics can reflect the characteristics of brain pathophysiology. However, the value of T1-weighted images, quantitative susceptibility mapping, and R2* mapping in the diagnosis of Parkinson's disease (PD) was underestimated in previous studies. In this prospective study to establish a...

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Published inNeural regeneration research Vol. 17; no. 12; pp. 2743 - 2749
Main Authors Guan, Xiao-Jun, Guo, Tao, Zhou, Cheng, Gao, Ting, Wu, Jing-Jing, Han, Victor, Cao, Steven, Wei, Hong-Jiang, Zhang, Yu-Yao, Xuan, Min, Gu, Quan-Quan, Huang, Pei-Yu, Liu, Chun-Lei, Pu, Jia-Li, Zhang, Bao-Rong, Cui, Feng, Xu, Xiao-Jun, Zhang, Min-Ming
Format Journal Article
LanguageEnglish
Published India Wolters Kluwer India Pvt. Ltd 01.12.2022
Medknow Publications & Media Pvt. Ltd
Department of Radiology,the Second Affiliated Hospital,Zhejiang University School of Medicine,Hangzhou,Zhejiang Province,China%Department of Neurology,the Second Affiliated Hospital,Zhejiang University School of Medicine,Hangzhou,Zhejiang Province,China%Department of Electrical Engineering and Computer Sciences,University of California,Berkeley,CA,USA%Institute for Medical Imaging Technology,School of Biomedical Engineering,Shanghai Jiao Tong University,Shanghai,China%School of Information Science and Technology,ShanghaiTech University,Shanghai,China%Department of Electrical Engineering and Computer Sciences,University of California,Berkeley,CA,USA
Helen Wills Neuroscience Institute,University of California,Berkeley,CA,USA%Department of Radiology,Hangzhou Hospital of Traditional Chinese Medicine,Hangzhou,Zhejiang Province,China
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ISSN1673-5374
1876-7958
DOI10.4103/1673-5374.339493

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Abstract Brain radiomics can reflect the characteristics of brain pathophysiology. However, the value of T1-weighted images, quantitative susceptibility mapping, and R2* mapping in the diagnosis of Parkinson's disease (PD) was underestimated in previous studies. In this prospective study to establish a model for PD diagnosis based on brain imaging information, we collected high-resolution T1-weighted images, R2* mapping, and quantitative susceptibility imaging data from 171 patients with PD and 179 healthy controls recruited from August 2014 to August 2019. According to the inclusion time, 123 PD patients and 121 healthy controls were assigned to train the diagnostic model, while the remaining 106 subjects were assigned to the external validation dataset. We extracted 1408 radiomics features, and then used data-driven feature selection to identify informative features that were significant for discriminating patients with PD from normal controls on the training dataset. The informative features so identified were then used to construct a diagnostic model for PD. The constructed model contained 36 informative radiomics features, mainly representing abnormal subcortical iron distribution (especially in the substantia nigra), structural disorganization (e.g., in the inferior temporal, paracentral, precuneus, insula, and precentral gyri), and texture misalignment in the subcortical nuclei (e.g., caudate, globus pallidus, and thalamus). The predictive accuracy of the established model was 81.1 ± 8.0% in the training dataset. On the external validation dataset, the established model showed predictive accuracy of 78.5 ± 2.1%. In the tests of identifying early and drug-naïve PD patients from healthy controls, the accuracies of the model constructed on the same 36 informative features were 80.3 ± 7.1% and 79.1 ± 6.5%, respectively, while the accuracies were 80.4 ± 6.3% and 82.9 ± 5.8% for diagnosing middle-to-late PD and those receiving drug management, respectively. The accuracies for predicting tremor-dominant and non-tremor-dominant PD were 79.8 ± 6.9% and 79.1 ± 6.5%, respectively. In conclusion, the multiple-tissue-specific brain radiomics model constructed from magnetic resonance imaging has the ability to discriminate PD and exhibits the advantages for improving PD diagnosis.
AbstractList Brain radiomics can reflect the characteristics of brain pathophysiology.However,the value of T1-weighted images,quantitative susceptibility mapping,and R2* mapping in the diagnosis of Parkinson's disease(PD)was underestimated in previous studies.In this prospective study to establish a model for PD diagnosis based on brain imaging information,we collected high-resolution T1-weighted images,R2* mapping,and quantitative susceptibility imaging data from 171 patients with PD and 179 healthy controls recruited from August 2014 to August 2019.According to the inclusion time,123 PD patients and 121 healthy controls were assigned to train the diagnostic model,while the remaining 106 subjects were assigned to the external validation dataset.We extracted 1408 radiomics features,and then used data-driven feature selection to identify informative features that were significant for discriminating patients with PD from normal controls on the training dataset.The informative features so identified were then used to construct a diagnostic model for PD.The constructed model contained 36 informative radiomics features,mainly representing abnormal subcortical iron distribution(especially in the substantia nigra),structural disorganization(e.g.,in the inferior temporal,paracentral,precuneus,insula,and precentral gyri),and texture misalignment in the subcortical nuclei(e.g.,caudate,globus pallidus,and thalamus).The predictive accuracy of the established model was 81.1±8.0%in the training dataset.On the external validation dataset,the established model showed predictive accuracy of 78.5±2.1%.In the tests of identifying early and drug-na?ve PD patients from healthy controls,the accuracies of the model constructed on the same 36 informative features were 80.3±7.1%and 79.1±6.5%,respectively,while the accuracies were 80.4±6.3%and 82.9±5.8%for diagnosing middle-to-late PD and those receiving drug management,respectively.The accuracies for predicting tremor-dominant and non-tremor-dominant PD were 79.8±6.9%and 79.1±6.5%,respectively.In conclusion,the multiple-tissue-specific brain radiomics model constructed from magnetic resonance imaging has the ability to discriminate PD and exhibits the advantages for improving PD diagnosis.
Brain radiomics can reflect the characteristics of brain pathophysiology. However, the value of T1-weighted images, quantitative susceptibility mapping, and R2* mapping in the diagnosis of Parkinson’s disease (PD) was underestimated in previous studies. In this prospective study to establish a model for PD diagnosis based on brain imaging information, we collected high-resolution T1-weighted images, R2* mapping, and quantitative susceptibility imaging data from 171 patients with PD and 179 healthy controls recruited from August 2014 to August 2019. According to the inclusion time, 123 PD patients and 121 healthy controls were assigned to train the diagnostic model, while the remaining 106 subjects were assigned to the external validation dataset. We extracted 1408 radiomics features, and then used data-driven feature selection to identify informative features that were significant for discriminating patients with PD from normal controls on the training dataset. The informative features so identified were then used to construct a diagnostic model for PD. The constructed model contained 36 informative radiomics features, mainly representing abnormal subcortical iron distribution (especially in the substantia nigra), structural disorganization (e.g., in the inferior temporal, paracentral, precuneus, insula, and precentral gyri), and texture misalignment in the subcortical nuclei (e.g., caudate, globus pallidus, and thalamus). The predictive accuracy of the established model was 81.1 ± 8.0% in the training dataset. On the external validation dataset, the established model showed predictive accuracy of 78.5 ± 2.1%. In the tests of identifying early and drug-naïve PD patients from healthy controls, the accuracies of the model constructed on the same 36 informative features were 80.3 ± 7.1% and 79.1 ± 6.5%, respectively, while the accuracies were 80.4 ± 6.3% and 82.9 ± 5.8% for diagnosing middle-to-late PD and those receiving drug management, respectively. The accuracies for predicting tremor-dominant and non-tremor-dominant PD were 79.8 ± 6.9% and 79.1 ± 6.5%, respectively. In conclusion, the multiple-tissue-specific brain radiomics model constructed from magnetic resonance imaging has the ability to discriminate PD and exhibits the advantages for improving PD diagnosis.
Brain radiomics can reflect the characteristics of brain pathophysiology. However, the value of T1-weighted images, quantitative susceptibility mapping, and R2* mapping in the diagnosis of Parkinson's disease (PD) was underestimated in previous studies. In this prospective study to establish a model for PD diagnosis based on brain imaging information, we collected high-resolution T1-weighted images, R2* mapping, and quantitative susceptibility imaging data from 171 patients with PD and 179 healthy controls recruited from August 2014 to August 2019. According to the inclusion time, 123 PD patients and 121 healthy controls were assigned to train the diagnostic model, while the remaining 106 subjects were assigned to the external validation dataset. We extracted 1408 radiomics features, and then used data-driven feature selection to identify informative features that were significant for discriminating patients with PD from normal controls on the training dataset. The informative features so identified were then used to construct a diagnostic model for PD. The constructed model contained 36 informative radiomics features, mainly representing abnormal subcortical iron distribution (especially in the substantia nigra), structural disorganization (e.g., in the inferior temporal, paracentral, precuneus, insula, and precentral gyri), and texture misalignment in the subcortical nuclei (e.g., caudate, globus pallidus, and thalamus). The predictive accuracy of the established model was 81.1 ± 8.0% in the training dataset. On the external validation dataset, the established model showed predictive accuracy of 78.5 ± 2.1%. In the tests of identifying early and drug-naïve PD patients from healthy controls, the accuracies of the model constructed on the same 36 informative features were 80.3 ± 7.1% and 79.1 ± 6.5%, respectively, while the accuracies were 80.4 ± 6.3% and 82.9 ± 5.8% for diagnosing middle-to-late PD and those receiving drug management, respectively. The accuracies for predicting tremor-dominant and non-tremor-dominant PD were 79.8 ± 6.9% and 79.1 ± 6.5%, respectively. In conclusion, the multiple-tissue-specific brain radiomics model constructed from magnetic resonance imaging has the ability to discriminate PD and exhibits the advantages for improving PD diagnosis.Brain radiomics can reflect the characteristics of brain pathophysiology. However, the value of T1-weighted images, quantitative susceptibility mapping, and R2* mapping in the diagnosis of Parkinson's disease (PD) was underestimated in previous studies. In this prospective study to establish a model for PD diagnosis based on brain imaging information, we collected high-resolution T1-weighted images, R2* mapping, and quantitative susceptibility imaging data from 171 patients with PD and 179 healthy controls recruited from August 2014 to August 2019. According to the inclusion time, 123 PD patients and 121 healthy controls were assigned to train the diagnostic model, while the remaining 106 subjects were assigned to the external validation dataset. We extracted 1408 radiomics features, and then used data-driven feature selection to identify informative features that were significant for discriminating patients with PD from normal controls on the training dataset. The informative features so identified were then used to construct a diagnostic model for PD. The constructed model contained 36 informative radiomics features, mainly representing abnormal subcortical iron distribution (especially in the substantia nigra), structural disorganization (e.g., in the inferior temporal, paracentral, precuneus, insula, and precentral gyri), and texture misalignment in the subcortical nuclei (e.g., caudate, globus pallidus, and thalamus). The predictive accuracy of the established model was 81.1 ± 8.0% in the training dataset. On the external validation dataset, the established model showed predictive accuracy of 78.5 ± 2.1%. In the tests of identifying early and drug-naïve PD patients from healthy controls, the accuracies of the model constructed on the same 36 informative features were 80.3 ± 7.1% and 79.1 ± 6.5%, respectively, while the accuracies were 80.4 ± 6.3% and 82.9 ± 5.8% for diagnosing middle-to-late PD and those receiving drug management, respectively. The accuracies for predicting tremor-dominant and non-tremor-dominant PD were 79.8 ± 6.9% and 79.1 ± 6.5%, respectively. In conclusion, the multiple-tissue-specific brain radiomics model constructed from magnetic resonance imaging has the ability to discriminate PD and exhibits the advantages for improving PD diagnosis.
Author Xuan, Min
Cao, Steven
Gu, Quan-Quan
Zhang, Yu-Yao
Zhang, Bao-Rong
Wei, Hong-Jiang
Guan, Xiao-Jun
Han, Victor
Zhou, Cheng
Huang, Pei-Yu
Pu, Jia-Li
Zhang, Min-Ming
Gao, Ting
Xu, Xiao-Jun
Cui, Feng
Liu, Chun-Lei
Wu, Jing-Jing
Guo, Tao
AuthorAffiliation Department of Radiology,the Second Affiliated Hospital,Zhejiang University School of Medicine,Hangzhou,Zhejiang Province,China%Department of Neurology,the Second Affiliated Hospital,Zhejiang University School of Medicine,Hangzhou,Zhejiang Province,China%Department of Electrical Engineering and Computer Sciences,University of California,Berkeley,CA,USA%Institute for Medical Imaging Technology,School of Biomedical Engineering,Shanghai Jiao Tong University,Shanghai,China%School of Information Science and Technology,ShanghaiTech University,Shanghai,China%Department of Electrical Engineering and Computer Sciences,University of California,Berkeley,CA,USA;Helen Wills Neuroscience Institute,University of California,Berkeley,CA,USA%Department of Radiology,Hangzhou Hospital of Traditional Chinese Medicine,Hangzhou,Zhejiang Province,China
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Issue 12
Keywords radiomics
magnetic resonance imaging
quantitative susceptibility mapping
imaging biomarker
T1-weighted imaging
diagnosis
iron
R2mapping
Parkinson’s disease
neuroimaging
Parkinson's disease
Language English
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Author contributions: Study conception: XJG, TG, XJX, MMZ; study organization: XJG, TG, MX, QQG, PYH, XJX, MMZ; experiment implementation: XJG, CZ, TG, JJW, VH, SC, HJW, YYZ, CLL, XJX, MMZ; statistical design: XJG, TG, TG, JJW, CLL, XJX, MMZ; statistical analysis: XJG, TG, CZ, VH, SC, HJW, YYZ, JLP, BRZ, FC; statistical revision: XJG, TG, CZ, TG, JJW, MX, QQG, PYH, CLL, JLP, BRZ, FC, XJX, MMZ; manuscript draft: XJG; manuscript revision: XJG, TG, CZ, TG, JJW, VH, SC, HJW, YYZ, MX, QQG, PYH, XJX, MMZ. All authors approved the final version of manuscript for publication.
Both authors contributed equally to this work.
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Department of Radiology,the Second Affiliated Hospital,Zhejiang University School of Medicine,Hangzhou,Zhejiang Province,China%Department of Neurology,the Second Affiliated Hospital,Zhejiang University School of Medicine,Hangzhou,Zhejiang Province,China%Department of Electrical Engineering and Computer Sciences,University of California,Berkeley,CA,USA%Institute for Medical Imaging Technology,School of Biomedical Engineering,Shanghai Jiao Tong University,Shanghai,China%School of Information Science and Technology,ShanghaiTech University,Shanghai,China%Department of Electrical Engineering and Computer Sciences,University of California,Berkeley,CA,USA
Helen Wills Neuroscience Institute,University of California,Berkeley,CA,USA%Department of Radiology,Hangzhou Hospital of Traditional Chinese Medicine,Hangzhou,Zhejiang Province,China
Wolters Kluwer - Medknow
Wolters Kluwer Medknow Publications
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– name: Department of Radiology,the Second Affiliated Hospital,Zhejiang University School of Medicine,Hangzhou,Zhejiang Province,China%Department of Neurology,the Second Affiliated Hospital,Zhejiang University School of Medicine,Hangzhou,Zhejiang Province,China%Department of Electrical Engineering and Computer Sciences,University of California,Berkeley,CA,USA%Institute for Medical Imaging Technology,School of Biomedical Engineering,Shanghai Jiao Tong University,Shanghai,China%School of Information Science and Technology,ShanghaiTech University,Shanghai,China%Department of Electrical Engineering and Computer Sciences,University of California,Berkeley,CA,USA
– name: Helen Wills Neuroscience Institute,University of California,Berkeley,CA,USA%Department of Radiology,Hangzhou Hospital of Traditional Chinese Medicine,Hangzhou,Zhejiang Province,China
– name: Wolters Kluwer - Medknow
– name: Wolters Kluwer Medknow Publications
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Snippet Brain radiomics can reflect the characteristics of brain pathophysiology. However, the value of T1-weighted images, quantitative susceptibility mapping, and...
Brain radiomics can reflect the characteristics of brain pathophysiology.However,the value of T1-weighted images,quantitative susceptibility mapping,and R2*...
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SubjectTerms Datasets
diagnosis; imaging biomarker; iron; magnetic resonance imaging; neuroimaging; parkinson’s disease; quantitative susceptibility mapping; r2 mapping; radiomics; t1-weighted imaging
Magnetic resonance imaging
Parkinson's disease
Radiomics
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Title A multiple-tissue-specific magnetic resonance imaging model for diagnosing Parkinson's disease: a brain radiomics study
URI http://www.nrronline.org/article.asp?issn=1673-5374;year=2022;volume=17;issue=12;spage=2743;epage=2749;aulast=Guan;type=0
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https://pubmed.ncbi.nlm.nih.gov/PMC9165377
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Volume 17
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