# Imaging-anchored multiomics in cardiovascular disease: integrating cardiac imaging, bulk, single-cell, and spatial transcriptomics

arXiv: https://arxiv.org/abs/2601.07871 · HTML: https://mlsanity.com/paper/2601.07871/

## Key facts

- No citing papers in the map yet (data through 14 Oct 2026).
- Builds on 20 of its 133 references that are in the map.
- First posted on arXiv 10 Jan 2026.

## Builds on (most cited first, 20 of 20)

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- [Multimodal Generative Models for Scalable Weakly-Supervised Learning](https://mlsanity.com/paper/1802.05335/) (2018)
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- [On Deep Multi-View Representation Learning: Objectives and Optimization](https://mlsanity.com/paper/1602.01024/) (2016)
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- [High-Throughput Precision Phenotyping of Left Ventricular Hypertrophy with Cardiovascular Deep Learning](https://mlsanity.com/paper/2106.12511/) (2021)
- [Multimodal contrastive learning for spatial gene expression prediction using histology images](https://mlsanity.com/paper/2407.08216/) (2024)
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- [Deep neural networks can predict mortality from 12-lead electrocardiogram voltage data](https://mlsanity.com/paper/1904.07032/) (2019)
- [Medical Multimodal Foundation Models in Clinical Diagnosis and Treatment: Applications, Challenges, and Future Directions](https://mlsanity.com/paper/2412.02621/) (2024)
- [Towards a vision foundation model for comprehensive assessment of Cardiac MRI](https://mlsanity.com/paper/2410.01665/) (2024)
- [Label-free segmentation from cardiac ultrasound using self-supervised learning](https://mlsanity.com/paper/2210.04979/) (2022)
- [HEIST: A Graph Foundation Model for Spatial Transcriptomics and Proteomics Data](https://mlsanity.com/paper/2506.11152/) (2025)
- [Generalized Product-of-Experts for Learning Multimodal Representations in Noisy Environments](https://mlsanity.com/paper/2211.03587/) (2022)
- [The Minimum Information about CLinical Artificial Intelligence Checklist for Generative Modeling Research (MI-CLAIM-GEN)](https://mlsanity.com/paper/2403.02558/) (2024)

## Abstract (arXiv)

Cardiovascular disease arises from interactions between inherited risk, molecular programmes, and tissue-scale remodelling that are observed clinically through imaging. Cardiac MRI (CMR), computed tomography (CT), and echocardiography are integral to routine cardiovascular care, while bulk RNA sequencing, single-cell RNA sequencing, and spatial transcriptomics are providing increasingly detailed molecular characterization of cardiac tissue. Yet, these imaging and molecular data are still analysed in largely separate pipelines. This review examines joint representations that link cardiac imaging phenotypes to transcriptomic and spatially resolved molecular states. An imaging-anchored perspective is adopted in which echocardiography, CMR, and CT define a spatial phenotype of the heart, and bulk, single-cell and spatial transcriptomics provide cell-type- and location-specific molecular context. We define the representation requirements of each modality, compare multimodal fusion strategies, and synthesize integrative pipelines for radiogenomics, spatial alignment, and image-based gene-expression prediction, together with their validation requirements, limitations, and failure modes. Spatial multiomic maps of human myocardium and atherosclerotic plaque, together with single-cell, spatial, and multimodal medical foundation models, are advancing imaging-anchored multiomics; however, cost, scalability, and tissue availability remain substantial barriers to large-scale cardiovascular translation.
