Mengyu Li , Magnús Magnússon , Ingibjörg Kristjánsdóttir , Sigrún Helga Lund , Thilo van Eimeren , Lotta M. Ellingsen , Alzheimer’s Disease Neuroimaging Initiative
{"title":"基于区域的U-nets用于快速、准确和可扩展的脑深部分割:在帕金森综合征中的应用","authors":"Mengyu Li , Magnús Magnússon , Ingibjörg Kristjánsdóttir , Sigrún Helga Lund , Thilo van Eimeren , Lotta M. Ellingsen , Alzheimer’s Disease Neuroimaging Initiative","doi":"10.1016/j.nicl.2025.103807","DOIUrl":null,"url":null,"abstract":"<div><div>The early diagnosis of age-related neurodegenerative diseases, which often progress to dementia, poses significant clinical challenges due to subtle and overlapping symptoms of these diseases at early stage. Automated MRI segmentation is important for early detection, as it offers consistent measurements and the ability to detect subtle structural changes in the brain. Manual segmentation is impractical for large datasets or clinical use. Deep learning approaches provide fast processing, however, they often encounter graphics processing unit (GPU) memory constraints when handling large datasets. Here we introduce a deep learning-based approach using region-based U-nets specifically designed to segment 12 deep-brain structures relevant to Parkinson Plus Syndromes. By dividing the brain image into targeted regions around the brainstem, ventricular system, and striatum, our method optimizes GPU usage and significantly reduces training times, while maintaining high accuracy. Validating the proposed method on three datasets, including a 660-subject clinical dataset comprising both healthy controls and patients with various movement disorders, we demonstrate robustness and practical applicability in separating different diseases. The method achieves superior segmentation performance compared to state-of-the-art methods, with a mean Dice Similarity Coefficient (DSC) of 0.90, a 95% Hausdorff Distance (HD95) of 1.35 mm, and an Average Symmetric Surface Distance (ASSD) of 0.45 mm, showcasing its segmentation accuracy and robustness. Furthermore, our method outperforms these methods by reducing training time from several days to a few hours while providing a processing time of less than a second per subject. The source code and trained model will be made publicly available on GitHub.</div></div>","PeriodicalId":54359,"journal":{"name":"Neuroimage-Clinical","volume":"47 ","pages":"Article 103807"},"PeriodicalIF":3.6000,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Region-based U-nets for fast, accurate, and scalable deep brain segmentation: Application to Parkinson Plus Syndromes\",\"authors\":\"Mengyu Li , Magnús Magnússon , Ingibjörg Kristjánsdóttir , Sigrún Helga Lund , Thilo van Eimeren , Lotta M. Ellingsen , Alzheimer’s Disease Neuroimaging Initiative\",\"doi\":\"10.1016/j.nicl.2025.103807\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>The early diagnosis of age-related neurodegenerative diseases, which often progress to dementia, poses significant clinical challenges due to subtle and overlapping symptoms of these diseases at early stage. Automated MRI segmentation is important for early detection, as it offers consistent measurements and the ability to detect subtle structural changes in the brain. Manual segmentation is impractical for large datasets or clinical use. Deep learning approaches provide fast processing, however, they often encounter graphics processing unit (GPU) memory constraints when handling large datasets. Here we introduce a deep learning-based approach using region-based U-nets specifically designed to segment 12 deep-brain structures relevant to Parkinson Plus Syndromes. By dividing the brain image into targeted regions around the brainstem, ventricular system, and striatum, our method optimizes GPU usage and significantly reduces training times, while maintaining high accuracy. Validating the proposed method on three datasets, including a 660-subject clinical dataset comprising both healthy controls and patients with various movement disorders, we demonstrate robustness and practical applicability in separating different diseases. The method achieves superior segmentation performance compared to state-of-the-art methods, with a mean Dice Similarity Coefficient (DSC) of 0.90, a 95% Hausdorff Distance (HD95) of 1.35 mm, and an Average Symmetric Surface Distance (ASSD) of 0.45 mm, showcasing its segmentation accuracy and robustness. Furthermore, our method outperforms these methods by reducing training time from several days to a few hours while providing a processing time of less than a second per subject. 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Region-based U-nets for fast, accurate, and scalable deep brain segmentation: Application to Parkinson Plus Syndromes
The early diagnosis of age-related neurodegenerative diseases, which often progress to dementia, poses significant clinical challenges due to subtle and overlapping symptoms of these diseases at early stage. Automated MRI segmentation is important for early detection, as it offers consistent measurements and the ability to detect subtle structural changes in the brain. Manual segmentation is impractical for large datasets or clinical use. Deep learning approaches provide fast processing, however, they often encounter graphics processing unit (GPU) memory constraints when handling large datasets. Here we introduce a deep learning-based approach using region-based U-nets specifically designed to segment 12 deep-brain structures relevant to Parkinson Plus Syndromes. By dividing the brain image into targeted regions around the brainstem, ventricular system, and striatum, our method optimizes GPU usage and significantly reduces training times, while maintaining high accuracy. Validating the proposed method on three datasets, including a 660-subject clinical dataset comprising both healthy controls and patients with various movement disorders, we demonstrate robustness and practical applicability in separating different diseases. The method achieves superior segmentation performance compared to state-of-the-art methods, with a mean Dice Similarity Coefficient (DSC) of 0.90, a 95% Hausdorff Distance (HD95) of 1.35 mm, and an Average Symmetric Surface Distance (ASSD) of 0.45 mm, showcasing its segmentation accuracy and robustness. Furthermore, our method outperforms these methods by reducing training time from several days to a few hours while providing a processing time of less than a second per subject. The source code and trained model will be made publicly available on GitHub.
期刊介绍:
NeuroImage: Clinical, a journal of diseases, disorders and syndromes involving the Nervous System, provides a vehicle for communicating important advances in the study of abnormal structure-function relationships of the human nervous system based on imaging.
The focus of NeuroImage: Clinical is on defining changes to the brain associated with primary neurologic and psychiatric diseases and disorders of the nervous system as well as behavioral syndromes and developmental conditions. The main criterion for judging papers is the extent of scientific advancement in the understanding of the pathophysiologic mechanisms of diseases and disorders, in identification of functional models that link clinical signs and symptoms with brain function and in the creation of image based tools applicable to a broad range of clinical needs including diagnosis, monitoring and tracking of illness, predicting therapeutic response and development of new treatments. Papers dealing with structure and function in animal models will also be considered if they reveal mechanisms that can be readily translated to human conditions.