用MRI和极低剂量PET生成高质量脑部PET图像,减少癫痫患者辐射暴露。
Score-based Generative Diffusion Models to Synthesize Full-dose FDG Brain PET from MRI in Epilepsy Patients
- 采用基于分数的生成扩散模型,从MRI数据合成FDG-PET图像。
- 仅用MRI即可生成接近全剂量的PET图像,全脑代谢比值误差最小。
- 结合1%低剂量PET输入后,三类模型性能均显著提升且效果相当。
氟代脱氧葡萄糖(FDG)PET用于癫痫患者评估是同步PET/MRI中最常见的应用之一,因需同时获取脑结构与代谢信息,但该群体年轻,辐射剂量问题突出。现有研究较少利用先进生成式AI方法(如扩散模型)从MRI或超低剂量PET数据中合成诊断级PET图像,并针对癫痫人群开展临床评估。本研究在52名受试者(40训练/2验证/10测试)的同步PET/MRI数据上,对比了两种基于分数的生成扩散模型(SGM-Karras Diffusion和SGM-方差保持)与Transformer-Unet在MRI到PET图像转换任务中的表现。评估包含标准图像指标及临床相关指标,如半球代谢不对称性评估指标(一致性指数与一致性平均绝对误差)。结果显示,仅使用T1w和T2 FLAIR图像时,SGM-KD在定量与定性方面均最优,全脑特异性摄取值比(SUVR)的平均绝对误差最低,组内相关系数最高。当输入中加入1%低剂量PET图像后,所有模型性能显著提升,定量与视觉质量可互换。结论表明,扩散模型在纯MRI到PET转换中潜力巨大,而三类模型均可通过融合MRI与超低剂量PET准确合成全剂量FDG-PET。
原文摘要 · Abstract (English)
Fluorodeoxyglucose (FDG) PET to evaluate patients with epilepsy is one of the most common applications for simultaneous PET/MRI, given the need to image both brain structure and metabolism, but is suboptimal due to the radiation dose in this young population. Little work has been done synthesizing diagnostic quality PET images from MRI data or MRI data with ultralow-dose PET using advanced generative AI methods, such as diffusion models, with attention to clinical evaluations tailored for the epilepsy population. Here we compared the performance of diffusion- and non-diffusion-based deep learning models for the MRI-to-PET image translation task for epilepsy imaging using simultaneous PET/MRI in 52 subjects (40 train/2 validate/10 hold-out test). We tested three different models: 2 score-based generative diffusion models (SGM-Karras Diffusion [SGM-KD] and SGM-variance preserving [SGM-VP]) and a Transformer-Unet. We report results on standard image processing metrics as well as clinically relevant metrics, including congruency measures (Congruence Index and Congruency Mean Absolute Error) that assess hemispheric metabolic asymmetry, which is a key part of the clinical analysis of these images. The SGM-KD produced the best qualitative and quantitative results when synthesizing PET purely from T1w and T2 FLAIR images with the least mean absolute error in whole-brain specific uptake value ratio (SUVR) and highest intraclass correlation coefficient. When 1% low-dose PET images are included in the inputs, all models improve significantly and are interchangeable for quantitative performance and visual quality. In summary, SGMs hold great potential for pure MRI-to-PET translation, while all 3 model types can synthesize full-dose FDG-PET accurately using MRI and ultralow-dose PET.
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