Enhancing Nigrosome-1 Sign Identification via Interpretable AI using True Susceptibility Weighted Imaging
© 2024 International Society for Magnetic Resonance in Medicine..
BACKGROUND: Nigrosome 1 (N1), the largest nigrosome region in the ventrolateral area of the substantia nigra pars compacta, is identifiable by the "N1 sign" in long echo time gradient echo MRI. The N1 sign's absence is a vital Parkinson's disease (PD) diagnostic marker. However, it is challenging to visualize and assess the N1 sign in clinical practice.
PURPOSE: To automatically detect the presence or absence of the N1 sign from true susceptibility weighted imaging by using deep-learning method.
STUDY TYPE: Prospective.
POPULATION/SUBJECTS: 453 subjects, including 225 PD patients, 120 healthy controls (HCs), and 108 patients with other movement disorders, were prospectively recruited including 227 males and 226 females. They were divided into training, validation, and test cohorts of 289, 73, and 91 cases, respectively.
FIELD STRENGTH/SEQUENCE: 3D gradient echo SWI sequence at 3T; 3D multiecho strategically acquired gradient echo imaging at 3T; NM-sensitive 3D gradient echo sequence with MTC pulse at 3T.
ASSESSMENT: A neuroradiologist with 5 years of experience manually delineated substantia nigra regions. Two raters with 2 and 36 years of experience assessed the N1 sign on true susceptibility weighted imaging (tSWI), QSM with high-pass filter, and magnitude data combined with MTC data. We proposed NINet, a neural model, for automatic N1 sign identification in tSWI images.
STATISTICAL TESTS: We compared the performance of NINet to the subjective reference standard using Receiver Operating Characteristic analyses, and a decision curve analysis assessed identification accuracy.
RESULTS: NINet achieved an area under the curve (AUC) of 0.87 (CI: 0.76-0.89) in N1 sign identification, surpassing other models and neuroradiologists. NINet localized the putative N1 sign within tSWI images with 67.3% accuracy.
DATA CONCLUSION: Our proposed NINet model's capability to determine the presence or absence of the N1 sign, along with its localization, holds promise for enhancing diagnostic accuracy when evaluating PD using MR images.
LEVEL OF EVIDENCE: 2 TECHNICAL EFFICACY: Stage 1.
| Medienart: |
E-Artikel |
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| Erscheinungsjahr: |
2024 |
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| Erschienen: |
2024 |
| Enthalten in: |
Zur Gesamtaufnahme - year:2024 |
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| Enthalten in: |
Journal of magnetic resonance imaging : JMRI - (2024) vom: 18. Jan. |
| Sprache: |
Englisch |
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| Beteiligte Personen: |
Wang, Chenglong [VerfasserIn] |
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| Links: |
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| Themen: |
Deep-learning |
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| Anmerkungen: |
Date Revised 18.01.2024 published: Print-Electronic Citation Status Publisher |
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| doi: |
10.1002/jmri.29245 |
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| funding: |
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| Förderinstitution / Projekttitel: |
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| PPN (Katalog-ID): |
NLM367270889 |
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| 100 | 1 | |a Wang, Chenglong |e verfasserin |4 aut | |
| 245 | 1 | 0 | |a Enhancing Nigrosome-1 Sign Identification via Interpretable AI using True Susceptibility Weighted Imaging |
| 264 | 1 | |c 2024 | |
| 336 | |a Text |b txt |2 rdacontent | ||
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| 500 | |a Date Revised 18.01.2024 | ||
| 500 | |a published: Print-Electronic | ||
| 500 | |a Citation Status Publisher | ||
| 520 | |a © 2024 International Society for Magnetic Resonance in Medicine. | ||
| 520 | |a BACKGROUND: Nigrosome 1 (N1), the largest nigrosome region in the ventrolateral area of the substantia nigra pars compacta, is identifiable by the "N1 sign" in long echo time gradient echo MRI. The N1 sign's absence is a vital Parkinson's disease (PD) diagnostic marker. However, it is challenging to visualize and assess the N1 sign in clinical practice | ||
| 520 | |a PURPOSE: To automatically detect the presence or absence of the N1 sign from true susceptibility weighted imaging by using deep-learning method | ||
| 520 | |a STUDY TYPE: Prospective | ||
| 520 | |a POPULATION/SUBJECTS: 453 subjects, including 225 PD patients, 120 healthy controls (HCs), and 108 patients with other movement disorders, were prospectively recruited including 227 males and 226 females. They were divided into training, validation, and test cohorts of 289, 73, and 91 cases, respectively | ||
| 520 | |a FIELD STRENGTH/SEQUENCE: 3D gradient echo SWI sequence at 3T; 3D multiecho strategically acquired gradient echo imaging at 3T; NM-sensitive 3D gradient echo sequence with MTC pulse at 3T | ||
| 520 | |a ASSESSMENT: A neuroradiologist with 5 years of experience manually delineated substantia nigra regions. Two raters with 2 and 36 years of experience assessed the N1 sign on true susceptibility weighted imaging (tSWI), QSM with high-pass filter, and magnitude data combined with MTC data. We proposed NINet, a neural model, for automatic N1 sign identification in tSWI images | ||
| 520 | |a STATISTICAL TESTS: We compared the performance of NINet to the subjective reference standard using Receiver Operating Characteristic analyses, and a decision curve analysis assessed identification accuracy | ||
| 520 | |a RESULTS: NINet achieved an area under the curve (AUC) of 0.87 (CI: 0.76-0.89) in N1 sign identification, surpassing other models and neuroradiologists. NINet localized the putative N1 sign within tSWI images with 67.3% accuracy | ||
| 520 | |a DATA CONCLUSION: Our proposed NINet model's capability to determine the presence or absence of the N1 sign, along with its localization, holds promise for enhancing diagnostic accuracy when evaluating PD using MR images | ||
| 520 | |a LEVEL OF EVIDENCE: 2 TECHNICAL EFFICACY: Stage 1 | ||
| 650 | 4 | |a Journal Article | |
| 650 | 4 | |a Parkinson's disease | |
| 650 | 4 | |a deep-learning | |
| 650 | 4 | |a nigrosome-1 | |
| 650 | 4 | |a substantia nigra | |
| 650 | 4 | |a true susceptibility weighted imaging | |
| 700 | 1 | |a He, Naying |e verfasserin |4 aut | |
| 700 | 1 | |a Zhang, Youmin |e verfasserin |4 aut | |
| 700 | 1 | |a Li, Yan |e verfasserin |4 aut | |
| 700 | 1 | |a Huang, Pei |e verfasserin |4 aut | |
| 700 | 1 | |a Liu, Yu |e verfasserin |4 aut | |
| 700 | 1 | |a Jin, Zhijia |e verfasserin |4 aut | |
| 700 | 1 | |a Cheng, Zenghui |e verfasserin |4 aut | |
| 700 | 1 | |a Liu, Yun |e verfasserin |4 aut | |
| 700 | 1 | |a Wang, Yida |e verfasserin |4 aut | |
| 700 | 1 | |a Zhang, Chengxiu |e verfasserin |4 aut | |
| 700 | 1 | |a Haacke, E Mark |e verfasserin |4 aut | |
| 700 | 1 | |a Chen, Shengdi |e verfasserin |4 aut | |
| 700 | 1 | |a Yan, Fuhua |e verfasserin |4 aut | |
| 700 | 1 | |a Yang, Guang |e verfasserin |4 aut | |
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