Department of Nuclear Medicine, Inselspital, Bern University Hospital, University of Bern , Bern, Switzerland.
Department of Informatics, Technische Universität München, Munich, Germany.
Eur J Nucl Med Mol Imaging. 2022 Jul;49(8):2798-2811. doi: 10.1007/s00259-022-05804-x. Epub 2022 May 19.
This work attempts to decode the discriminative information in dopamine transporter (DAT) imaging using deep learning for the differential diagnosis of parkinsonism.
This study involved 1017 subjects who underwent DAT PET imaging ([C]CFT) including 43 healthy subjects and 974 parkinsonian patients with idiopathic Parkinson's disease (IPD), multiple system atrophy (MSA) or progressive supranuclear palsy (PSP). We developed a 3D deep convolutional neural network to learn distinguishable DAT features for the differential diagnosis of parkinsonism. A full-gradient saliency map approach was employed to investigate the functional basis related to the decision mechanism of the network. Furthermore, deep-learning-guided radiomics features and quantitative analysis were compared with their conventional counterparts to further interpret the performance of deep learning.
The proposed network achieved area under the curve of 0.953 (sensitivity 87.7%, specificity 93.2%), 0.948 (sensitivity 93.7%, specificity 97.5%), and 0.900 (sensitivity 81.5%, specificity 93.7%) in the cross-validation, together with sensitivity of 90.7%, 84.1%, 78.6% and specificity of 88.4%, 97.5% 93.3% in the blind test for the differential diagnosis of IPD, MSA and PSP, respectively. The saliency map demonstrated the most contributed areas determining the diagnosis located at parkinsonism-related regions, e.g., putamen, caudate and midbrain. The deep-learning-guided binding ratios showed significant differences among IPD, MSA and PSP groups (P < 0.001), while the conventional putamen and caudate binding ratios had no significant difference between IPD and MSA (P = 0.24 and P = 0.30). Furthermore, compared to conventional radiomics features, there existed average above 78.1% more deep-learning-guided radiomics features that had significant differences among IPD, MSA and PSP.
This study suggested the developed deep neural network can decode in-depth information from DAT and showed potential to assist the differential diagnosis of parkinsonism. The functional regions supporting the diagnosis decision were generally consistent with known parkinsonian pathology but provided more specific guidance for feature selection and quantitative analysis.
本研究旨在利用深度学习技术从多巴胺转运体(DAT)成像中解码鉴别信息,以辅助帕金森病的鉴别诊断。
本研究纳入了 1017 例接受 [C]CFT 多巴胺转运体 PET 成像的受试者,包括 43 例健康对照者和 974 例帕金森病(特发性帕金森病,IPD)、多系统萎缩(MSA)或进行性核上性麻痹(PSP)患者。我们开发了一个 3D 深度卷积神经网络,以学习有助于帕金森病鉴别诊断的可区分 DAT 特征。采用全梯度显著性映射方法探讨与网络决策机制相关的功能基础。此外,还比较了深度学习指导的放射组学特征和定量分析,以进一步解释深度学习的性能。
在交叉验证中,所提出的网络在鉴别诊断 IPD、MSA 和 PSP 中的曲线下面积分别为 0.953(敏感性 87.7%,特异性 93.2%)、0.948(敏感性 93.7%,特异性 97.5%)和 0.900(敏感性 81.5%,特异性 93.7%),在盲测中,用于鉴别诊断 IPD、MSA 和 PSP 的敏感性分别为 90.7%、84.1%和 78.6%,特异性分别为 88.4%、97.5%和 93.3%。显著性映射显示,对诊断最有贡献的区域位于帕金森病相关区域,如壳核、尾状核和中脑。深度学习指导的结合率在 IPD、MSA 和 PSP 组之间存在显著差异(P<0.001),而传统的壳核和尾状核结合率在 IPD 和 MSA 之间无显著差异(P=0.24 和 P=0.30)。此外,与传统的放射组学特征相比,深度学习指导的放射组学特征中有 78.1%以上具有显著差异。
本研究表明,所开发的深度神经网络可以从 DAT 中解码深入信息,并有望辅助帕金森病的鉴别诊断。支持诊断决策的功能区域与已知的帕金森病病理基本一致,但为特征选择和定量分析提供了更具体的指导。