Parameter-efficient adaptation of foundational models for automated myocardial strain analysis
Clinical Snapshot
PICO Framework
| P — Population | Adult subjects undergoing cardiac MRI across multiple datasets (four public, one private; >900 subjects total), including healthy volunteers and patients with known cardiac disease |
| I — Intervention | CardiacSAM — a parameter-efficient adaptation of the Segment Anything Model (SAM) using Low-Rank Adaptation (LoRA) for cardiac segmentation, paired with uniGradICON for myocardial motion estimation and global strain computation in short-axis (SAX) and long-axis (LAX) views |
| C — Comparator | Cross-dataset generalisation benchmarked against expert landmark annotations and reference versus disease group discrimination; SAX versus LAX strain correlation analysis in 360 subjects |
| O — Outcomes | Left ventricular (LV) Dice segmentation score; median average endpoint error (AEPE) for motion estimation; global myocardial strain values (radial and longitudinal); discrimination between reference and disease groups; correlation between SAX- and LAX-derived strain measures |
Bottom Line
CardiacSAM represents a technically innovative approach to automated myocardial strain analysis, leveraging parameter-efficient fine-tuning of the Segment Anything Model to achieve acceptable LV segmentation performance (Dice 0.90) with as few as 10 training cases per domain. The cross-dataset validation across five cohorts (>900 subjects) is a meaningful strength, and the low data requirement addresses a genuine barrier to clinical deployment of deep learning tools across heterogeneous imaging environments. However, several critical limitations temper enthusiasm. Motion estimation was validated in only 15 healthy volunteers — an inadequate sample for a tool intended for pathological populations. The weak SAX-LAX longitudinal strain correlation (r=0.17) is unexplained and raises legitimate concerns about measurement validity. No confidence intervals are reported, no comparison with established clinical strain methods is provided, and no prospective clinical validation has been performed. For Australian clinicians, TGA SaMD approval and MBS integration would be prerequisites for clinical use. This work is best characterised as a promising proof-of-concept requiring independent prospective validation before any clinical deployment can be considered. Senior clinicians should not alter practice based on this study alone.
Key Findings
P Value: Strain group discrimination described as statistically significant; specific p-values not provided in abstract
Effect Size: Mean LV Dice score 0.90±0.02 (SAX, 10 training studies); median AEPE 3.08 mm for motion estimation; SAX-LAX radial strain correlation r=0.64; SAX-LAX longitudinal strain correlation r=0.17
Primary Outcome: LV segmentation Dice score and myocardial strain discrimination between reference and disease groups across five datasets
Nnt Or Sensitivity: Diagnostic accuracy metrics (sensitivity, specificity, AUC) not reported; no NNT applicable to this methodological study; Dice coefficient of 0.90 as primary segmentation performance indicator
Confidence Interval: Not reported for any outcome measure
Clinical Application
The low training data requirement (10 studies for SAX domain adaptation) is a practical advantage for smaller centres or novel scanner deployments. However, clinical deployment would require regulatory approval, integration with existing PACS/CMR workflows, prospective validation in target patient populations, and demonstration of non-inferiority to established strain methods. The pipeline's computational requirements are not described. Cardiac MRI with myocardial strain analysis is performed across major Australian tertiary centres and is relevant to the management of cardiomyopathies, chemotherapy-related cardiotoxicity monitoring, and valvular heart disease assessment. The RACGP and CSANZ do not currently provide specific guidelines on automated AI-based strain analysis tools. TGA regulatory approval as a Software as a Medical Device (SaMD) under the ARTG would be required before clinical deployment in Australia. PBS reimbursement for CMR is limited and context-specific; automated strain tools would need to demonstrate cost-effectiveness within the MBS framework (MBS item 63399 and related cardiac MRI items). Australian CMR practice predominantly uses 1.5T and 3T scanners from major vendors; cross-vendor validation would be essential. The data efficiency advantage of this approach could benefit regional and rural Australian centres with smaller CMR volumes. Adult patients undergoing cardiac MRI for assessment of myocardial function, particularly in settings where automated strain analysis is sought across heterogeneous scanner environments or institutions with limited labelled training data
Abstract
Purpose. Automated myocardial strain analysis requires accurate segmentation and motion tracking, but deep learning methods trained on one dataset often fail when applied to images from different scanners or institutions. We investigate how general-purpose foundational models can be efficiently adapted for cardiac strain estimation, establishing the minimal data requirements for robust cross-domain deployment.Methods. We propose CardiacSAM, a lightweight adaptation of the Segment Anything Model (SAM) fine-tuned with Low-Rank Adaptation, for cardiac structure segmentation, paired with uniGradICON for myocardial motion estimation. We compute global strain in cardiac coordinates for both short-axis (SAX) and long-axis (LAX) views.Results. Validated on four public and one private dataset comprising over 900 subjects, CardiacSAM achieved mean left ventricle (LV) Dice scores of0.90±0.02using only 10 training studies per domain for SAX (50 for LAX). Motion estimation achieved median average endpoint error (AEPE) of 3.08 mm on 15 volunteers without known cardiac disease with expert landmark annotations. Strain measurements discriminated significantly between reference and disease groups across all datasets. Comparing SAX and LAX strain in 360 subjects showed moderate correlation for radial strain (r=0.64) but weak correlation for longitudinal strain (r=0.17), suggesting SAX and LAX capture complementary information about cardiac function.Conclusion. Parameter-efficient adaptation of foundational models enables automated cardiac strain assessment with high data efficiency and robust cross-dataset generalization.
References
- 1.Bernardo, A., Mato, G., Calandrelli, M., Medus, J., & Curiale, A. (2026). Parameter-efficient adaptation of foundational models for automated myocardial strain analysis. Biomedical Physics & Engineering Express. https://doi.org/10.1088/2057-1976/ae7c09
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