用深度学习从PET图像预测动脉输入函数,免去小鼠采血
A robust and versatile deep learning model for prediction of the arterial input function in dynamic small animal $\left[^{18}\text{F}\right]$FDG PET imaging
- 基于卷积神经网络,从动态PET图像直接预测动脉输入函数
- 在多种扫描条件下误差低,相关性高,且对时序偏移和截断数据鲁棒
- 适用于[18F]FDG,但对其他示踪剂需重新训练
动态正电子发射断层扫描(PET)与动力学建模对小动物示踪剂研发至关重要。准确建模依赖于精确的动脉输入函数(AIF)估计,传统方法需动脉采血,但操作复杂、耗时且为终末性,难以开展纵向研究。本文提出一种非侵入式全卷积深度学习模型(FC-DLIF),可直接从PET影像预测AIF,有望替代采血。该模型包含空间特征提取器和时间特征提取器,分别处理体积时间序列中的空间信息与时间动态。模型在[18F]FDG数据上通过交叉验证训练与评估,并扩展至[18F]FDOPA和[68Ga]PSMA两种示踪剂数据。进一步测试显示,模型在扫描截断或时移情况下仍能可靠预测AIF。然而,未在训练中包含的示踪剂无法准确预测。结果表明,该深度学习方法为动脉采血提供了非侵入、可靠且对时序变化鲁棒的替代方案。
原文摘要 · Abstract (English)
Dynamic positron emission tomography (PET) and kinetic modeling are pivotal in advancing tracer development research in small animal studies. Accurate kinetic modeling requires precise input function estimation, traditionally achieved via arterial blood sampling. However, arterial cannulation in small animals like mice, involves intricate, time-consuming, and terminal procedures, precluding longitudinal studies. This work proposes a non-invasive, fully convolutional deep learning-based approach (FC-DLIF) to predict input functions directly from PET imaging, potentially eliminating the need for blood sampling in dynamic small-animal PET. The proposed FC-DLIF model includes a spatial feature extractor acting on the volumetric time frames of the PET sequence, extracting spatial features. These are subsequently further processed in a temporal feature extractor that predicts the arterial input function. The proposed approach is trained and evaluated using images and arterial blood curves from [$^{18}$F]FDG data using cross validation. Further, the model applicability is evaluated on imaging data and arterial blood curves collected using two additional radiotracers ([$^{18}$F]FDOPA, and [$^{68}$Ga]PSMA). The model was further evaluated on data truncated and shifted in time, to simulate shorter, and shifted, PET scans. The proposed FC-DLIF model reliably predicts the arterial input function with respect to mean squared error and correlation. Furthermore, the FC-DLIF model is able to predict the arterial input function even from truncated and shifted samples. The model fails to predict the AIF from samples collected using different radiotracers, as these are not represented in the training data. Our deep learning-based input function offers a non-invasive and reliable alternative to arterial blood sampling, proving robust and flexible to temporal shifts and different scan durations.
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