应用深度学习模型诊断血红素/伊红染色心肌组织淀粉样变性。

European heart journal. Imaging methods and practice Pub Date : 2024-12-30 eCollection Date: 2025-01-01 DOI:10.1093/ehjimp/qyae141
Takeshi Tohyama, Takeshi Iwasaki, Masataka Ikeda, Masato Katsuki, Tatsuya Watanabe, Kayo Misumi, Keisuke Shinohara, Takeo Fujino, Toru Hashimoto, Shouji Matsushima, Tomomi Ide, Junji Kishimoto, Koji Todaka, Yoshinao Oda, Kohtaro Abe
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引用次数: 0

摘要

目的:心肌组织淀粉样蛋白沉积是诊断心脏淀粉样变性的明确特征,尽管骨示踪心脏显像和心脏磁共振成像等侵入性较小的成像方式已被确立为诊断的第一步。本研究旨在建立一个深度学习模型,以支持从血红素/伊红(HE)染色的心肌组织中诊断心脏淀粉样变性。方法和结果:这项单中心回顾性观察性研究纳入了166名在2008年至2022年间接受心肌活组织检查的患者,其中76名诊断为心脏淀粉样变性,90名诊断为其他诊断。开发了一个深度学习模型来输出从每个心肌标本中切出的所有小斑块的心脏淀粉样变的概率。该模型突出显示了染色图像中的高度可疑区域,对应于Dylon染色标记淀粉样蛋白沉积的区域,并以曲线下面积为0.965来区分评价数据集中的斑块。假设将心脏淀粉样变性的诊断标准定义为所有斑块中发生心脏淀粉样变性的中位数概率>50%,则该模型在区分心脏淀粉样变性患者和非心脏淀粉样变性患者方面表现良好,曲线下面积为1.0。结论:建立了一种能够准确诊断心肌淀粉样变性的深度学习模型。虽然需要使用来自多个中心的he染色心肌组织对该模型进行进一步的前瞻性验证,但它可能有助于减少心脏淀粉样变性缺失的风险,并在临床实践中最大化组织学诊断的效用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Deep learning model to diagnose cardiac amyloidosis from haematoxylin/eosin-stained myocardial tissue.

Aims: Amyloid deposition in myocardial tissue is a definitive feature for diagnosing cardiac amyloidosis, though less invasive imaging modalities such as bone tracer cardiac scintigraphy and cardiac magnetic resonance imaging have been established as first steps for its diagnosis. This study aimed to develop a deep learning model to support the diagnosis of cardiac amyloidosis from haematoxylin/eosin (HE)-stained myocardial tissue.

Methods and results: This single-centre retrospective observational study enrolled 166 patients who underwent myocardial biopsies between 2008 and 2022, including 76 patients diagnosed with cardiac amyloidosis and 90 with other diagnoses. A deep learning model was developed to output the probabilities of cardiac amyloidosis for all the small patches cutout from each myocardial specimen. The developed model highlighted the area in the stained images as highly suspicious, corresponding to where Dylon staining marked amyloid deposition, and discriminated the patches in the evaluation dataset with an area under the curve of 0.965. Provided that the diagnostic criterion for cardiac amyloidosis was defined as a median probability of cardiac amyloidosis >50% in all patches, the model achieved perfect performance in discriminating patients with cardiac amyloidosis from those without it, with an area under the curve of 1.0.

Conclusion: A deep learning model was developed to diagnose cardiac amyloidosis from HE-stained myocardial tissue accurately. Although further prospective validation of this model using HE-stained myocardial tissues from multiple centres is needed, it may help minimize the risk of missing cardiac amyloidosis and maximize the utility of histological diagnosis in clinical practice.

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