Fast and scalable localisation of a left ventricle (LV)-centered region of interest (ROI) is essential for cardiac image analysis, particularly in stress perfusion cardiovascular magnetic resonance (CMR), where manual annotation is time-consuming and labelled datasets are scarce. This study proposes a fully automated, annotation-free pipeline that integrates Fast Fourier Transform-based localisation, Sobel edge refinement, and a fallback heuristic to generate consistent LV-centered ROIs directly from raw perfusion frames, without requiring task-specific annotations. A circular ROI is applied as a post-processing step to ensure consistent coverage of the ventricular cavity and surrounding myocardium while preserving diagnostically relevant boundary information. To assess whether learning-based models can replicate these pseudo-annotations without perfusion-specific training, a clinician-verified subset of 295 FFT-Sobel annotations was used to benchmark a pretrained U-Net and a one-shot similarity model. The FFT + Sobel method achieved successful ROI localisation in 81.5% of 460 frames at 0.002 s per frame. The U-Net achieved a Dice score of 88.6% and IoU of 80.1%, but only 72% full ROI detection, while the one-shot model showed limited spatial agreement (Dice 26.7%, IoU 16.8%). These findings demonstrate that the proposed classical pipeline provides a fast, robust, and scalable solution for LV-centered ROI localisation in annotation-free perfusion CMR, offering a consistent and clinically meaningful representation for downstream cardiac image analysis.

Fast and scalable annotation-free LV-centered ROI localisation in stress perfusion cardiac MRI / Kalashami, Mahsa Pourhossein; Fagioli, Alessio; Marini, Marco Raoul; Elshibly, Mohamed; Shergill, Simran; Mccann, Gerry P.; Arnold, J. Ranjit; Statharas, Dimitrios. - In: COMPUTERS IN BIOLOGY AND MEDICINE. - ISSN 0010-4825. - 211:(2026). [10.1016/j.compbiomed.2026.111747]

Fast and scalable annotation-free LV-centered ROI localisation in stress perfusion cardiac MRI

Fagioli, Alessio;Marini, Marco Raoul;
2026

Abstract

Fast and scalable localisation of a left ventricle (LV)-centered region of interest (ROI) is essential for cardiac image analysis, particularly in stress perfusion cardiovascular magnetic resonance (CMR), where manual annotation is time-consuming and labelled datasets are scarce. This study proposes a fully automated, annotation-free pipeline that integrates Fast Fourier Transform-based localisation, Sobel edge refinement, and a fallback heuristic to generate consistent LV-centered ROIs directly from raw perfusion frames, without requiring task-specific annotations. A circular ROI is applied as a post-processing step to ensure consistent coverage of the ventricular cavity and surrounding myocardium while preserving diagnostically relevant boundary information. To assess whether learning-based models can replicate these pseudo-annotations without perfusion-specific training, a clinician-verified subset of 295 FFT-Sobel annotations was used to benchmark a pretrained U-Net and a one-shot similarity model. The FFT + Sobel method achieved successful ROI localisation in 81.5% of 460 frames at 0.002 s per frame. The U-Net achieved a Dice score of 88.6% and IoU of 80.1%, but only 72% full ROI detection, while the one-shot model showed limited spatial agreement (Dice 26.7%, IoU 16.8%). These findings demonstrate that the proposed classical pipeline provides a fast, robust, and scalable solution for LV-centered ROI localisation in annotation-free perfusion CMR, offering a consistent and clinically meaningful representation for downstream cardiac image analysis.
2026
Annotation-free segmentation; ROI detection in MRI; Left ventricle localisation; Medical image processing; Automated image annotation
01 Pubblicazione su rivista::01a Articolo in rivista
Fast and scalable annotation-free LV-centered ROI localisation in stress perfusion cardiac MRI / Kalashami, Mahsa Pourhossein; Fagioli, Alessio; Marini, Marco Raoul; Elshibly, Mohamed; Shergill, Simran; Mccann, Gerry P.; Arnold, J. Ranjit; Statharas, Dimitrios. - In: COMPUTERS IN BIOLOGY AND MEDICINE. - ISSN 0010-4825. - 211:(2026). [10.1016/j.compbiomed.2026.111747]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11573/1768224
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