A selective kernel-based cycle-consistent generative adversarial network for unpaired low-dose CT denoising

IF 5.1 4区 医学 Q1 MEDICINE, RESEARCH & EXPERIMENTAL Precision Clinical Medicine Pub Date : 2022-04-20 DOI:10.1093/pcmedi/pbac011
C. Tan, Mingming Yang, Zhisheng You, Hu Chen, Yan Zhang
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引用次数: 9

Abstract

Abstract Low-dose computed tomography (LDCT) denoising is an indispensable procedure in the medical imaging field, which not only improves image quality, but can mitigate the potential hazard to patients caused by routine doses. Despite the improvement in performance of the cycle-consistent generative adversarial network (CycleGAN) due to the well-paired CT images shortage, there is still a need to further reduce image noise while retaining detailed features. Inspired by the residual encoder–decoder convolutional neural network (RED-CNN) and U-Net, we propose a novel unsupervised model using CycleGAN for LDCT imaging, which injects a two-sided network into selective kernel networks (SK-NET) to adaptively select features, and uses the patchGAN discriminator to generate CT images with more detail maintenance, aided by added perceptual loss. Based on patch-based training, the experimental results demonstrated that the proposed SKFCycleGAN outperforms competing methods in both a clinical dataset and the Mayo dataset. The main advantages of our method lie in noise suppression and edge preservation.
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非配对低剂量CT去噪的基于选择性核的周期一致生成对抗网络
摘要低剂量计算机断层扫描(LDCT)去噪是医学成像领域不可或缺的一项技术,不仅可以提高图像质量,而且可以减轻常规剂量对患者的潜在危害。尽管周期一致生成对抗网络(CycleGAN)由于缺乏良好配对的CT图像而提高了性能,但仍需要在保留细节特征的同时进一步降低图像噪声。受残差编码器-解码器卷积神经网络(RED-CNN)和U-Net的启发,我们提出了一种基于CycleGAN的LDCT成像无监督模型,该模型在选择性核网络(SK-NET)中注入一个双边网络自适应选择特征,并使用patchGAN鉴别器生成具有更多细节维护的CT图像,同时增加了感知损失。基于补丁训练的实验结果表明,所提出的SKFCycleGAN在临床数据集和Mayo数据集上都优于竞争对手的方法。该方法的主要优点在于噪声抑制和边缘保持。
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来源期刊
Precision Clinical Medicine
Precision Clinical Medicine MEDICINE, RESEARCH & EXPERIMENTAL-
CiteScore
10.80
自引率
0.00%
发文量
26
审稿时长
5 weeks
期刊介绍: Precision Clinical Medicine (PCM) is an international, peer-reviewed, open access journal that provides timely publication of original research articles, case reports, reviews, editorials, and perspectives across the spectrum of precision medicine. The journal's mission is to deliver new theories, methods, and evidence that enhance disease diagnosis, treatment, prevention, and prognosis, thereby establishing a vital communication platform for clinicians and researchers that has the potential to transform medical practice. PCM encompasses all facets of precision medicine, which involves personalized approaches to diagnosis, treatment, and prevention, tailored to individual patients or patient subgroups based on their unique genetic, phenotypic, or psychosocial profiles. The clinical conditions addressed by the journal include a wide range of areas such as cancer, infectious diseases, inherited diseases, complex diseases, and rare diseases.
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