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Translation of atherosclerotic disease features onto healthy carotid ultrasound images using domain-to-domain translation.
- Source :
- Biomedical Signal Processing & Control; Aug2023, Vol. 85, pN.PAG-N.PAG, 1p
- Publication Year :
- 2023
-
Abstract
- In this work, we evaluated a model for the translation of atherosclerotic disease features onto healthy carotid ultrasound images. An un-paired domain-to-domain translation model – the cycle Generative Adversarial Network (cycleGAN) – was trained to translate between carotid ultrasound images of healthy arteries and images of pronounced disease. Translation performance was evaluated using the measurement of wall thickness in original and generated images. In addition, we explored disease translation in different tissue segments (subcutaneous tissue, muscle, lumen, far wall, and deep tissues), using structural similarity index measure (SSIM) maps. Features of pronounced disease were successfully translated to the healthy images (1.2 (0.33) mm vs 0.43 (0.07) mm, p < 0.001), while overall anatomy was retained as SSIM value was equal to 0.78 (0.02). Exploration of translated features showed that both arterial wall and subcutaneous tissues were modified in the translation, but that the subcutaneous tissue was subject to distortion of the anatomy in some cases. The image quality influenced the disease translation performance. The results show that the model can learn a mapping between healthy and diseased images while retaining the overall anatomical contents. This is the first study on atherosclerosis disease translation in medical images. The concept of translating disease onto existing healthy images may serve purposes such as education, cardiovascular risk communication in health conversations, or personalized modelling in precision medicine. [ABSTRACT FROM AUTHOR]
Details
- Language :
- English
- ISSN :
- 17468094
- Volume :
- 85
- Database :
- Supplemental Index
- Journal :
- Biomedical Signal Processing & Control
- Publication Type :
- Academic Journal
- Accession number :
- 164304106
- Full Text :
- https://doi.org/10.1016/j.bspc.2023.104886