1)江苏理工学院机械工程学院,常州 213001;2)南京航空航天大学机电学院,南京 210016;3)华南理工大学未来技术学院,广州 510641;4)暨南大学物理与光电工程学院,广州 510632
江苏省国际合作项目(BZ2024036),江苏省高校自然科学重大研究项目(24KJA460003),江苏省常州市应用基础研究计划(CJ20241070)和江苏理工学院研究生实践创新计划项目 (XSJCX25_14)资助。
1)College of Mechanical Engineering, Jiangsu University of Technology, Changzhou 213001, China;2)College of Mechanical and Electrical Engineering, Nanjing University of Aeronautics and Astronautics, Nanjing 210016, China;3)School of Future Technology, South China University of Technology, Guangzhou 510641, China;4)College of Physics and Optoelectronic Engineering, Jinan University, Guangzhou 510632, China
This work was supported by grants from the International Cooperation Project of Jiangsu Province (BZ2024036), the Major Research Project of Natural Science for Universities in Jiangsu Province (24KJA460003), the Applied Basic Research Program of Changzhou, Jiangsu Province (CJ20241070), and the Postgraduate Practice Innovation Program of Jiangsu University of Technology (XSJCX25_14).
目的 针对电阻抗断层成像(electrical impedance tomography,EIT)在乳腺筛查应用中因逆问题的严重病态性导致的重建精度不足、小目标检测能力弱,以及现有深度学习方法训练效率低、缺乏物理一致性等问题,提出一种面向乳腺筛查场景的多尺度注意力与动态稀疏掩码融合网络(multi-scale attention and dynamic sparse mask network,MADS-Net),以实现高分辨率EIT图像重建。方法 网络采用“先定位、后重建”策略,通过动态掩码模块实现计算资源自适应分配,利用多尺度注意力机制缓解映射过程中的信息丢失,并嵌入物理约束提升结果合理性。通过系统仿真、琼脂体模与猪肉组织实验验证方法性能,与高斯-牛顿、卷积神经网络、U-Net、Deep D-Bar等主流方法开展对比,以图像相关系数(image correlation coefficient,ICC)、均方根误差(root mean square error,RMSE)、峰值信噪比(peak signal-to-noise ratio,PSNR)为定量评价指标。结果 MADS-Net在全测试场景中性能优于对比方法,平均ICC达0.917 6±0.048 8,RMSE低至0.060 6±0.031 6,PSNR达(23.893 9±2.685 3)dB;可在直径100 mm的传感场内成功检出5 mm小目标,训练时长缩短23.5%,同时具备优异的噪声鲁棒性。结论 MADS-Net在仿真、琼脂体模和离体猪肉组织实验中表现出较好的EIT重建性能,为EIT技术在乳腺筛查相关场景及其他医学功能成像任务中的进一步研究提供了方法学参考。需要指出的是,本研究尚未使用真实临床乳腺数据进行验证,其临床适用性仍需进一步研究。
Objective To address the key challenges in breast electrical impedance tomography (EIT) reconstruction including the severe ill-posedness of the inverse problem, limited measurement information from the electrodes, low contrast of small lesions, as well as the common drawbacks of traditional reconstruction methods such as boundary blurring, low spatial resolution, and weak small-target detection capability, and to overcome the limitations of existing deep learning approaches namely low training efficiency, insufficient physical consistency, and substantial information loss during the low-to-high dimensional mapping process, this study proposes a multi-scale attention and dynamic sparse mask fusion network (MADS-Net). The proposed method aims to enhance high-resolution reconstruction accuracy, small-lesion detectability, noise robustness, and computational efficiency in breast-screening-oriented EIT, thereby providing a feasible solution for the application of EIT in breast functional imaging.Methods The proposed network adopts a strategy of “locate first, reconstruct later”. It realizes adaptive allocation of computational resources through a dynamic mask module, alleviates information loss in the low-to-high dimensional mapping process via a multi-scale attention mechanism, and embeds physical constraints to improve the physical rationality of reconstruction results. The performance of the proposed method was validated through systematic numerical simulations, agar phantom experiments, and porcine tissue experiments. Comparisons were made with mainstream methods including the Gauss-Newton algorithm, convolutional neural networks, U-Net, and Deep D-Bar. The image correlation coefficient (ICC), root mean square error (RMSE), and peak signal-to-noise ratio (PSNR) were adopted as quantitative evaluation metrics. Furthermore, lesion-level evaluation metrics were introduced to assess the capability of different methods in reconstructing abnormal target boundaries and small-sized target regions.Results Experimental results demonstrate that MADS-Net outperforms all comparison methods across all test scenarios. In numerical simulations, it achieves higher accuracy in target morphology and spatial location recovery as well as better background suppression. In agar phantom experiments, its detection and imaging reliability for small targets is significantly superior to the comparison methods. In porcine tissue experiments, the model maintains good generalization performance and can adapt to complex biological tissue imaging scenarios. Quantitative results show that MADS-Net achieves an average ICC of 0.917 6±0.048 8, an RMSE as low as 0.060 6±0.031 6, and a PSNR of (23.893 9±2.685 3) dB. It successfully detects tiny targets as small as 5 mm within a 100 mm diameter sensing field, reduces the total training duration by 23.5% compared with the baseline method, and maintains stable reconstruction performance even under strong noise interference.Conclusion The results demonstrate that MADS-Net achieves favorable EIT reconstruction performance in numerical simulations, agar phantom experiments, and porcine tissue experiments, even under common practical imaging challenges including low signal-to-noise ratio and blurred tissue boundaries. This study provides a methodological reference for further research on EIT in breast-screening-related scenarios and other medical functional imaging tasks, and also offers a low-cost, radiation-free alternative for breast lesion screening that aligns with the clinical demand for non-invasive diagnostic tools. It should be noted that real clinical breast data have not yet been used for validation in this study, and the clinical applicability of the proposed method requires further investigation. Future work will prioritize collecting multi-center real clinical breast datasets, and further optimize the model’s generalization ability to adapt to individual differences in breast tissue composition to promote its clinical application.
俞成涛,王佳卉,胡松佩,陈怀瑾,丁力,叶霞,姚佳烽. MADS-Net:面向乳腺筛查电阻抗断层成像重建的多尺度注意力与动态稀疏掩码融合网络[J].生物化学与生物物理进展,2026,53(9):2480-2496 YU Cheng-Tao, WANG Jia-Hui, HU Song-Pei, CHEN Huai-Jin, DING Li, YE Xia, YAO Jia-Feng. MADS-Net: a Multi-scale Attention and Dynamic Sparse Mask Fusion Network for Electrical Impedance Tomography Image Reconstruction in Breast Screening[J]. Progress in Biochemistry and Biophysics,2026,53(9):2480-2496
复制

扫码关注 生物化学与生物物理进展 ® 2026 网站版权 ICP:京ICP备05023138号-1 京公网安备 11010502031771号
