Keywords: AI/ML Image Reconstruction, Machine Learning/Artificial Intelligence, Federated learning, multi-institutional, collaborative learning, image reconstruction
Motivation: Federated learning (FL) enables privacy-preserving training of deep reconstruction models across multiple sites to improve generalization at the expense of lower within-site performance. Yet, existing methods require a common model architecture across sites, limiting flexibility.
Goal(s): Our goal was to devise an architecture-agnostic method for collaborative training of heterogeneous models across sites.
Approach: We introduced a novel peer-to-peer generative learning method (PGL-FedMR), where individual sites share a generative prior for their MRI data with remaining sites, and prior-driven synthetic data are used to train reconstruction models at each site.
Results: PGL-FedMR improves across-site generalization over local models, and within-site performance over conventional FL.
Impact: Improvements in within-site and across-site performance for MRI reconstruction through PGL-FedMR, coupled with the ability to handle heterogeneous architectures, may facilitate privacy-preserving multi-institutional collaborations to build reliable reconstruction models for many applications where data are scarce including rare diseases.
1. Lustig, M., Donoho, D., Pauly, J.M., “Sparse MRI: The application of compressed sensing for rapid MR imaging,” Magn. Reson. Med., vol. 58, no. 6, pp. 1182–1195, 2007.
2. Haldar, J.P., Hernando, D., Liang, Z.P., “Compressed-sensing MRI with random encoding,” IEEE Trans. Med. Imaging, vol. 30, no. 4, pp. 893–903, 2010.
3. Wang, S., Su, Z., Ying, L., Peng, X., Zhu, S., Liang, F., Feng, D., Liang, D., “Accelerating magnetic resonance imaging via deep learning,” in IEEE 13th Int. Symp. Biomed. Imaging (ISBI), 2016, pp. 514–517.
4. Hammernik H., Klatzer T., Kobler R., Recht M.P., Sodickson D.K., Pock T., Knoll F., “Learning a variational network for reconstruction of accelerated MRI data,” Magn. Reson. Med., vol. 79, no. 6, pp. 3055–3071, 2018.
5. Zhu, B., Liu, J.Z., Rosen, B.R., Rosen, M.S., “Image reconstruction by domain transform manifold learning,” Nature, vol. 555, no. 7697, pp. 487–492, 2018.
6. Qin, C., Schlemper, J., Caballero, J., Price, A.N., Hajnal, J.V., Rueckert, D., “Convolutional recurrent neural networks for dynamic MR image reconstruction,” IEEE Trans. Med. Imaging, vol. 38, no. 1, pp. 280–290, 2018.
7. Mardani, M., Gong, E., Cheng, J.Y., Vasanawala, S.S., Zaharchuk, G., Xing, L., Pauly. J.M., “Deep Generative Adversarial Neural Networks for Compressive Sensing MRI,” IEEE Trans. Med. Imaging, vol. 38, no. 1, pp. 167-179, 2019.
8. Akçakaya, M, Moeller, S, Weingärtner, S, Uğurbil, K., “Scan-specific robust artificial-neural-networks for k-space interpolation (RAKI) reconstruction Database-free deep learning for fast imaging,” Magn. Reson. Med., vol. 81, pp. 439–453, 2019.
9. Tamir, J.I., Yu S., Lustig. M., “Unsupervised deep basis pursuit: Learning reconstruction without ground-truth data,” in Proceedings of ISMRM, 2019, p. 0660.
10. Aggarwal H.K., Mani, M.P., Jacob, M., “MoDL: Model-Based Deep Learning Architecture for Inverse Problems,” IEEE Trans. Med. Imaging, vol. 38, no. 2, pp. 394–405, 2019.
11. Peng, X., Sutton, B.P., Lam, F., Liang, Z.P., “DeepSENSE: Learning coil sensitivity functions for SENSE reconstruction using deep learning,” Magn. Reson. Med., vol. 87, no. 4, pp. 1894–1902, 2020.
12. Kuestner, T., Fuin, N., Hammernik, K., Bustin, A., Qi, H., Hajhosseiny, R., Masci, P. G., Neji, R., Rueckert, D., Botnar, R. M., Prieto, C., “CINENet: deep learning-based 3D cardiac CINE MRI reconstruction with multi-coil complex-valued 4D spatio-temporal convolutions,” Scientific Reports, vol. 10, no. 1, 2020.
13. Polak, D., Cauley, S., Bilgic, B., Gong, E., Bachert, P., Adalsteinsson, E., Setsompop, K., “Joint multi-contrast variational network reconstruction (jVN) with application to rapid 2D and 3D imaging,” Magn. Reson. Med., vol. 84, no. 3, pp. 1456–1469, 2020.
14. Eo, T., Jun, Y., Kim, T., Jang, J., Lee, H. J., Hwang, D., “KIKI-net: cross-domain convolutional neural networks for reconstructing undersampled magnetic resonance images,” Magn. Reson. Med., vol. 80, no. 5, pp. 2188–2201, 2018.
15. Dar, S.U., Yurt, M., Shahdloo, M., Ildız, M.E., Tınaz, B., Cukur, T., “Prior-Guided Image Reconstruction for Accelerated Multi-Contrast MRI via Generative Adversarial Networks,” IEEE J. Sel. Top. Signal Process., vol. 14, no. 6, pp. 1072–1087, 2020.
16. Liu, F., Feng, L., Kijowski, R., “MANTIS: Model-Augmented Neural neTwork with Incoherent k-space Sampling for efficient MR parameter mapping,” Magn. Reson. Med., vol. 82, no. 1, pp. 174–188, 2019.
17. Guo, P., Wang, P., Zhou, J., Jiang, S., Patel, V.M., “Multi-institutional Collaborations for Improving Deep Learning-based Magnetic Resonance Image Reconstruction Using Federated Learning,” arXiv:2103.02148, 2021.
18. G. A. Kaissis, M. R. Makowski, D. Rueckert, R. F. Braren, “Secure, privacy-preserving and federated machine learning in medical imaging,” Nat. Mach. Intelli., vol. 2, no. 6, pp. 305–311, 2020.
19. N. Rieke, J. Hancox, W. Li, F. Milletar, H. R. Roth, S. Albarqouni, S. Bakas et al., “The future of digital health with federated learning,” NPJ Digit. Med., vol. 3, no. 1, p. 119, 2020.
20. X. Li, Y. Gu, N. Dvornek, L. H. Staib, P. Ventola, J. S. Duncan, “Multi-site fmri analysis using privacy-preserving federated learning and domain adaptation: Abide results,” Med. Image Anal., vol. 65, p. 101765, 2020.
21. Rajagopal A, Redekop E, Kemisetti A, Kulkarni R, Raman S, Sarma K, Magudia K, Arnold CW, Larson PEZ, “Federated Learning with Research Prototypes: Application to Multi-Center MRI-based Detection of Prostate Cancer with Diverse Histopathology,” Acad Radiol., vol. 30, no. 4, pp. 644-657, 2023.
22. Elmas, G, Dar, SUH, Korkmaz, Y, Ceyani, E, Susam, B, Ozbey, M, Avestimehr, S, Çukur, T. Federated Learning of Generative Image Priors for MRI Reconstruction. IEEE Trans. Med. Imaging. vol. 42, no. 7, pp. 1996-2009, 2023.
23. Feng C.M., Yan Y., Wang S., Xu, Y., Shao, L., Fu, H. “Specificity-Preserving Federated Learning for MR Image Reconstruction,” arXiv:2112.05752v3, 2022.
24. Levac, B.R., Arvinte, M., Tamir, J.I., "Federated End-to-End Unrolled Models for Magnetic Resonance Image Reconstruction," Bioengineering, vol. 10, no. 3, p. 364, 2023.
25. Dalmaz, O., Mirza, U., Elmas, G., Ozbey, M., Dar, SUH., Ceyani, E., Avestimehr, S., Çukur, T, “One model to unite them all: Personalized federated learning of multi-contrast MRI synthesis,” arXiv:2207.06509, 2022.
26. Wu, R., Li, C., Zou, J., Wang, S., “FedAutoMRI: Federated Neural Architecture Search for MR Image Reconstruction,” arXiv:2307.11538, 2023.
27. Menze, B.H., Jakab, A., Bauer, S., Kalpathy-Cramer, J., Farahani, K., Kirby, J., et al. "The Multimodal Brain Tumor Image Segmentation Benchmark (BRATS)," IEEE Trans. Med. Imaging, vol. 34, no. 10, pp. 1993-2024, 2015.
28. F. Knoll, J. Zbontar, A. Sriram, M. J. Muckley, M. Bruno, A. Defazio, M. Parente et al., “fastMRI: A publicly available raw k-space and DICOM dataset of knee images for accelerated MR image reconstruction using machine learning,” Rad. Artif. Intell., vol. 2, no. 1, p. e190007, 2020.
29. R. Souza, O. Lucena, J. Garrafa, D. Gobbi, M. Saluzzi, S. Appenzeller, L. Rittner, R. Frayne, R. Lotufo, “An open, multi-vendor, multi-field strength brain MR dataset and analysis of publicly available skull stripping methods agreement,” NeuroImage, vol. 170, pp. 482–494, 2018.
30. Uecker, M., Lai, P., Murphy, M.J., Virtue, P., Elad, M., Pauly, J.M., Vasanawala, S.S., Lustig, M., “ESPIRiT--an eigenvalue approach to autocalibrating parallel MRI: where SENSE meets GRAPPA,” Magn. Reson. Med., vol. 71, no. 3, pp. 990–1001, 2014.