LST-AI: A deep learning ensemble for accurate MS lesion segmentation

IF 3.4 2区 医学 Q2 NEUROIMAGING Neuroimage-Clinical Pub Date : 2024-01-01 DOI:10.1016/j.nicl.2024.103611
Tun Wiltgen , Julian McGinnis , Sarah Schlaeger , Florian Kofler , CuiCi Voon , Achim Berthele , Daria Bischl , Lioba Grundl , Nikolaus Will , Marie Metz , David Schinz , Dominik Sepp , Philipp Prucker , Benita Schmitz-Koep , Claus Zimmer , Bjoern Menze , Daniel Rueckert , Bernhard Hemmer , Jan Kirschke , Mark Mühlau , Benedikt Wiestler
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Abstract

Automated segmentation of brain white matter lesions is crucial for both clinical assessment and scientific research in multiple sclerosis (MS). Over a decade ago, we introduced an engineered lesion segmentation tool, LST. While recent lesion segmentation approaches have leveraged artificial intelligence (AI), they often remain proprietary and difficult to adopt. As an open-source tool, we present LST-AI, an advanced deep learning-based extension of LST that consists of an ensemble of three 3D U-Nets.

LST-AI explicitly addresses the imbalance between white matter (WM) lesions and non-lesioned WM. It employs a composite loss function incorporating binary cross-entropy and Tversky loss to improve segmentation of the highly heterogeneous MS lesions. We train the network ensemble on 491 MS pairs of T1-weighted and FLAIR images, collected in-house from a 3T MRI scanner, and expert neuroradiologists manually segmented the utilized lesion maps for training. LST-AI also includes a lesion location annotation tool, labeling lesions as periventricular, infratentorial, and juxtacortical according to the 2017 McDonald criteria, and, additionally, as subcortical. We conduct evaluations on 103 test cases consisting of publicly available data using the Anima segmentation validation tools and compare LST-AI with several publicly available lesion segmentation models.

Our empirical analysis shows that LST-AI achieves superior performance compared to existing methods. Its Dice and F1 scores exceeded 0.62, outperforming LST, SAMSEG (Sequence Adaptive Multimodal SEGmentation), and the popular nnUNet framework, which all scored below 0.56. Notably, LST-AI demonstrated exceptional performance on the MSSEG-1 challenge dataset, an international WM lesion segmentation challenge, with a Dice score of 0.65 and an F1 score of 0.63—surpassing all other competing models at the time of the challenge. With increasing lesion volume, the lesion detection rate rapidly increased with a detection rate of >75% for lesions with a volume between 10 mm3 and 100 mm3. Given its higher segmentation performance, we recommend that research groups currently using LST transition to LST-AI. To facilitate broad adoption, we are releasing LST-AI as an open-source model, available as a command-line tool, dockerized container, or Python script, enabling diverse applications across multiple platforms.

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LST-AI:用于准确分割多发性硬化症病灶的深度学习集合
脑白质病变的自动分割对于多发性硬化症(MS)的临床评估和科学研究都至关重要。十多年前,我们推出了一种工程病灶分割工具 LST。虽然最近的病灶分割方法利用了人工智能(AI),但它们往往仍然是专有的,难以采用。作为一款开源工具,我们推出了 LST-AI,它是 LST 基于深度学习的高级扩展,由三个三维 U-Nets 组成。LST-AI 明确解决了白质(WM)病变和非病变 WM 之间的不平衡问题,它采用了一种包含二元交叉熵和 Tversky 损失的复合损失函数,以改善高度异质性 MS 病变的分割。我们在内部 3T 磁共振成像扫描仪收集的 491 对 MS T1 加权和 FLAIR 图像上训练网络集合,并由神经放射学专家手动分割用于训练的病灶图。LST-AI 还包括病灶位置标注工具,可根据 2017 年 McDonald 标准将病灶标注为脑室周围、脑室下和并皮质,此外还可标注为皮质下。我们使用Anima分割验证工具对103个由公开数据组成的测试案例进行了评估,并将LST-AI与几种公开的病灶分割模型进行了比较。其 Dice 和 F1 分数超过 0.62,优于 LST、SAMSEG(序列自适应多模态 SEGmentation)和流行的 nnUNet 框架,它们的分数都低于 0.56。值得注意的是,LST-AI 在国际 WM 病灶分割挑战赛 MSSEG-1 数据集上表现优异,Dice 得分为 0.65,F1 得分为 0.63,超越了当时所有其他竞争模型。随着病变体积的增大,病变检测率迅速提高,体积在 10 立方毫米到 100 立方毫米之间的病变检测率达到 75%。鉴于其较高的分割性能,我们建议目前使用 LST 的研究小组过渡到 LST-AI。为便于广泛采用,我们将以开源模式发布 LST-AI,可作为命令行工具、docker 化容器或 Python 脚本使用,从而实现跨平台的多样化应用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Neuroimage-Clinical
Neuroimage-Clinical NEUROIMAGING-
CiteScore
7.50
自引率
4.80%
发文量
368
审稿时长
52 days
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.
期刊最新文献
Corrigendum to "Quantitative susceptibility mapping in multiple sclerosis: A systematic review and meta-analysis" [Neuroimage: Clin. 42 (2024) 103598]. Corrigendum to "Association between clinical features and decreased degree centrality and variability in dynamic functional connectivity in the obsessive-compulsive disorder" [Neuroimage: Clinical 44 (2024) 1-9/103665]. Corrigendum to "Impact of adult-onset multiple sclerosis on MRI-based intracranial volume: A study in clinically discordant monozygotic twins" [NeuroImage Clin. 42 (2024) 103597]. Neurometabolic alterations in children and adolescents with functional neurological disorder Preoperative plasticity in the functional naming network of patients with left insular gliomas
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