Medical imaging datasets are inherently high dimensional with large variability and low sample sizes that limit the effectiveness of deep learning algorithms. Recently, generative adversarial networks (GANs) with the ability to synthesize realist images have shown great potential as an alternative to standard data augmentation techniques. Our work focuses on cross-modality synthesis of fluorodeoxyglucose~(FDG) Positron Emission Tomography~(PET) scans from structural Magnetic Resonance~(MR) images using generative models to facilitate multi-modal diagnosis of Alzheimer's disease (AD). Specifically, we propose a novel end-to-end, globally and locally aware image-to-image translation GAN (GLA-GAN) with a multi-path architecture that enforces both global structural integrity and fidelity to local details. We further supplement the standard adversarial loss with voxel-level intensity, multi-scale structural similarity (MS-SSIM) and region-of-interest (ROI) based loss components that reduce reconstruction error, enforce structural consistency at different scales and perceive variation in regional sensitivity to AD respectively. Experimental results demonstrate that our GLA-GAN not only generates synthesized FDG-PET scans with enhanced image quality but also superior clinical utility in improving AD diagnosis compared to state-of-the-art models. Finally, we attempt to interpret some of the internal units of the GAN that are closely related to this specific cross-modality generation task.
翻译:医学成像数据集本质上是高维的,具有巨大的变异性和低样本规模,限制了深层学习算法的有效性。最近,具有综合现实图像能力的基因对抗网络(GANs)作为标准数据增强技术的替代物,显示出巨大的潜力。我们的工作重点是将含氟脱氧溶胶~(FDG)活性气球排放托声学~(PET)扫描的跨模式合成成像,利用基因模型对结构磁共振~(MR)图像进行超模化分析,以便利对阿尔茨海默氏病(AD)进行多式诊断。具体而言,我们提议建立一个具有全球和地方意识的图像模拟网络(GANs),作为标准数据增强结构完整性和对当地细节的忠诚性。我们进一步补充标准对抗性损失,利用基于基因共振荡的模型(MS-SSIM)和地区性利益单位(ROI)进行标准性测试,以减少重建错误,在不同尺度上实施结构一致性,并感知到在区域对GA-A(G-A)具体用途分析质量进行更高级的试算。我们G-A-A-A-AG(C)的临床分析,最后的实验结果显示我们对G-A-AD-A-A-AG-G-G-G-C-G-C-C-C-C-C-C-C-C-C-C-C-C-C-C-C-C-C-G-C-C-C-C-C-C-C-C-C-C-C-C-C-C-C-C-C-C-C-C-C-C-C-C-C-C-C-C-C-C-C-C-C-C-C-C-C-C-C-C-C-C-C-C-C-C-C-C-C-C-C-C-C-C-C-C-C-C-C-C-C-C-C-C-C-C-C-C-C-C-C-C-C-C-C-C-C-C-C-C-C-C-C-C-C-C-C-C-C-C-C-C-C-C