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Updated: Aug 5, 2026

Multimodal Study of Murine Cardiovascular Remodeling: Four-Dimensional Ultrasound and Mass Spectrometry Imaging
Published on: January 10, 2025
Imaging-anchored multiomics in cardiovascular disease: integrating cardiac imaging, bulk, single-cell, and spatial
Minh H N Le1, Thanh-Huy Nguyen2, Tao Li3
1Section of Cardiovascular Medicine, Department of Internal Medicine, Yale School of Medicine, 333 Cedar Street, New Haven, CT 06510, United States.
Insights
Integrating cardiac imaging (echocardiography, CMR, CT) with molecular data (RNA sequencing, spatial transcriptomics) offers new insights into cardiovascular disease. This review explores methods to link imaging phenotypes with molecular states for better understanding and treatment.
Area of Science:
- Cardiovascular research
- Medical imaging
- Genomics and transcriptomics
Background:
- Cardiovascular disease (CVD) involves complex interactions between genetic risk, molecular processes, and tissue changes.
- Clinical imaging (echocardiography, cardiac MRI, CT) and molecular profiling (RNA sequencing, spatial transcriptomics) are crucial for CVD diagnosis and research.
- Current analysis pipelines for imaging and molecular data are largely separate, limiting integrated insights.
Purpose of the Study:
- To review joint representations linking cardiac imaging phenotypes to transcriptomic and spatially resolved molecular states.
- To adopt an imaging-anchored perspective, integrating echocardiography, CMR, and CT with molecular data for spatial context.
- To explore integrative pipelines for radiogenomics and image-based gene-expression prediction.
Main Methods:
- Examining representation requirements for cardiac imaging and transcriptomic modalities.
- Comparing multimodal fusion strategies for integrating diverse data types.
- Synthesizing integrative pipelines for radiogenomics, spatial alignment, and gene-expression prediction.
Main Results:
- Development of joint representations linking imaging phenotypes to molecular states.
- Advancement in spatial multiomic maps and multimodal medical foundation models for cardiac research.
- Identification of integrative pipelines for radiogenomics and image-based gene-expression prediction.
Conclusions:
- Integrating cardiac imaging and molecular data through joint representations enhances understanding of CVD.
- Spatial multiomics and advanced models are progressing imaging-anchored multiomics in cardiology.
- Cost, scalability, and tissue availability remain significant challenges for widespread clinical translation.
Abstract:
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.
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