A U of M Medical School treatment concept offers a first targeted treatment option for those with HFpEF

MINNEAPOLIS/ST. PAUL (10/19/2021) - Recent studies may point towards a new therapeutic mechanism for a type of heart failure that currently has no specific treatment option. Researchers from the University of Minnesota Medical School — along with the University of Vermont and the Medical University of South Carolina — looked into a condition called heart failure with a preserved ejection fraction, or HFpEF. They discovered a mechanism that could prove useful in this common, yet hard-to-treat, condition.

“Heart failure is among the most common reasons for hospital admissions in developed countries, and about half of these patients have HFpEF, which is a type of heart failure with a normal cardiac pump function but a stiffened heart muscle,” said Markus Meyer, MD, an associate professor of medicine at the U of M Medical School. “This new approach reduces the exposure to increased cardiac stiffness.”

Meyer is the lead author of the report, which was published in Circulation. In their research, Meyer and his team built upon recent clinical studies that have shown improvements in HFpEF patients who took milrinone and levosimendan. These two medications are sometimes used to strengthen cardiac contraction in patients with heart failure and a reduced pump function. 

In their study, Meyer and team found that:

  • These benefits were associated with lower-filling pressures inside the heart chambers; 

  • All interventions activate calcium cycling, which controls cardiac contraction and relaxation; and

  • Calcium cycling leads to a baseline heart muscle tone, which prevents the overfilling of the heart and exposure to high levels of stiffness that result in heart failure symptoms. 

Recognition of this therapeutic mechanism may lay the foundation for a more tailored management of these patients who have been proven to derive few benefits from standard heart failure treatments. 

However, it remains to be seen if the short-term benefits over several weeks translate into improved long-term outcomes. Meyer said further research is needed to confirm the validity of this conceptual framework as laid out by the research team, and there are already several ongoing pacing and medication studies that test this concept at the U of M Medical School and the University of Vermont.

“Although these very encouraging results may provide a real step forward, we should remain cautious,” Meyer said. “It will be very important that we select the right patients and ascertain that these treatments are safe and indeed reduce heart failure in the long run.”

The co-authors of this study are Martin M. LeWinter, MD, of the University of Vermont Medical Center, and Michael R. Zile, MD, of the Medical University of South Carolina. 

This research was funded by the National Institutes of Health, the Engdahl Family Foundation at the University of Minnesota, the Martin LeWinter Young Investigator Fund and Medtronic. 


About the University of Minnesota Medical School
The University of Minnesota Medical School is at the forefront of learning and discovery, transforming medical care and educating the next generation of physicians. Our graduates and faculty produce high-impact biomedical research and advance the practice of medicine. We acknowledge that the U of M Medical School, both the Twin Cities campus and Duluth campus, is located on traditional, ancestral and contemporary lands of the Dakota and the Ojibwe, and scores of other Indigenous people, and we affirm our commitment to tribal communities and their sovereignty as we seek to improve and strengthen our relations with tribal nations. For more information about the U of M Medical School, please visit med.umn.edu

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