Cardiomyopathy, a principal contributor to heart failure and sudden cardiac mortality, demands precise early screening. Cardiac Magnetic Resonance (CMR), recognized as the diagnostic “gold standard” through multiparametric protocols, holds the potential to serve as an accurate screening tool. However, its reliance on gadolinium contrast and labor-intensive interpretation hinders population-scale deployment. We propose CC-CMR, a Contrastive Learning and Cross-Modal alignment framework for gadolinium-free cardiomyopathy screening using cine CMR sequences. By aligning the latent spaces of cine CMR and Late Gadolinium Enhancement (LGE) sequences, our model encodes fibrosis-specific pathology into cine CMR embeddings. A Feature Interaction Module concurrently optimizes diagnostic precision and cross-modal feature congruence, augmented by an uncertainty-guided adaptive training mechanism that dynamically calibrates task-specific objectives to ensure model generalizability. Evaluated on multi-center data from 231 subjects, CC-CMR achieves accuracy of 0.943 (95% CI: 0.886–0.986), outperforming state-of-the-art cine-CMR-only models by 4.3% while eliminating gadolinium dependency, demonstrating its clinical viability for wide range of populations and healthcare environments.

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LGE-Guided Cross-Modality Contrastive Learning for Gadolinium-Free Cardiomyopathy Screening in Cine CMR

  • Siqing Yuan,
  • Yulin Wang,
  • Zirui Cao,
  • Yueyan Wang,
  • Zehao Weng,
  • Hui Wang,
  • Lei Xu,
  • Zixian Chen,
  • Lei Chen,
  • Zhong Xue,
  • Dinggang Shen

摘要

Cardiomyopathy, a principal contributor to heart failure and sudden cardiac mortality, demands precise early screening. Cardiac Magnetic Resonance (CMR), recognized as the diagnostic “gold standard” through multiparametric protocols, holds the potential to serve as an accurate screening tool. However, its reliance on gadolinium contrast and labor-intensive interpretation hinders population-scale deployment. We propose CC-CMR, a Contrastive Learning and Cross-Modal alignment framework for gadolinium-free cardiomyopathy screening using cine CMR sequences. By aligning the latent spaces of cine CMR and Late Gadolinium Enhancement (LGE) sequences, our model encodes fibrosis-specific pathology into cine CMR embeddings. A Feature Interaction Module concurrently optimizes diagnostic precision and cross-modal feature congruence, augmented by an uncertainty-guided adaptive training mechanism that dynamically calibrates task-specific objectives to ensure model generalizability. Evaluated on multi-center data from 231 subjects, CC-CMR achieves accuracy of 0.943 (95% CI: 0.886–0.986), outperforming state-of-the-art cine-CMR-only models by 4.3% while eliminating gadolinium dependency, demonstrating its clinical viability for wide range of populations and healthcare environments.