Correcting cardiac microdomains to reverse non-ischemic heart failure
Official title: Correcting Cardiac Microdomains Reverses Non-Ischemic Cardiomyopathy
Funded at Utah State Higher Education System--University of Utah · NIH-11330515 · Data updated 2026-11-12
A gene therapy approach targeting calcium-handling microdomains in the heart is being tested to restore heart function in a large animal model of non-ischemic cardiomyopathy.
Quick facts
| Grant type | R01 grant |
|---|---|
| Study type | NIH-funded research |
| Funding institution | Utah State Higher Education System--University of Utah NIH-funded |
| Lab location | 1 site (Salt Lake City, United States) |
| Project start | August 5, 2023 |
| Project end | April 30, 2027 |
| Funding year | 2026 |
| Award (this year) | $616,000 |
| NIH project number | 5R01HL170196-04 |
| Project ID | NIH-11330515 on NIH RePORTER |
Who could benefit from this research
✓Could help
Ideal candidates are individuals with non-ischemic heart failure due to disrupted calcium handling who could participate in future translational studies.
✕Less likely to help
Patients with non-cardiac conditions or heart failure due to ischemic disease may not benefit from this specific approach.
What this research studies
This project tests a gene therapy strategy aimed at rebuilding the tiny structures that control calcium signaling in heart cells, which often become defective in heart failure. Researchers will use a minipig model of pacing-induced heart failure to see if delivering cBIN1 can restore microdomain organization and improve heart function. They will combine biochemical analyses and advanced imaging to understand how the therapy affects cardiomyocyte structure and calcium handling. If successful, this work could pave the way for translating a promising therapy toward human trials for non-ischemic heart failure.
Why it matters
Potential benefit: If successful, patients with non-ischemic heart failure might benefit from a new gene therapy that improves heart muscle cell function and overall heart performance.
How similar studies have gone: Prior rodent studies showed that exogenous cBIN1 can rescue heart failure; translation to a large animal model is a critical step toward human trials.
Where this research is happening
-
Utah State Higher Education System--University of Utah
Salt Lake City, United States Active
Researchers
- Principal investigator: Shaw, Robin M — Utah State Higher Education System--University of Utah
- Study coordinator: Shaw, Robin M
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About this research
- This is an active NIH-funded research project — typically early-stage science, not a clinical trial accepting patient enrollment.
- Some NIH-funded labs run parallel clinical studies or seek volunteers for related work. To check, contact the principal investigator or institution listed above.
- For full project details, budget, and progress reports, visit the official NIH RePORTER page.