The potential implications of the team’s discovery were startling enough that it prompted investigators to check and recheck the data for the reality of the findings to set in.
“When the observation was first reported to me I didn’t believe it,” Yutzey says. “I’ve had three different postdocs work on this now, trying to show the same finding in different ways, and finally it became evident that it was working.
“The old dogma was you can’t get new heart muscle, and now we and some other groups in the field are finding that you can,” she says. “The question is how you make that work so it’s therapeutically beneficial to patients.”
High-risk, higher stakes
The research clearly falls into a high-risk category, which essentially means the chances of failure are considerable, according to Yutzey. Also considerable are the potentially high benefits if the research leads to useful therapies.
According to the U.S. Centers for Disease Control and Prevention, unhealed heart attack damage is the leading cause of heart failure, contributing to 287,000 deaths a year in the United States alone. Meanwhile, congenital heart defects affect about one percent—or about 40,000—births a year in the U.S. The estimated hospital costs for people with congenital heart disease exceeds $1.9 billion.
And while today’s advancing surgical techniques can reconfigure some malformed hearts to allow more children born with cardiac defects to survive into adulthood, those survivors often need complex, life-long follow-up care.
When age matters
One of the questions Yutzey and her colleagues want to answer is what age and health status would be best for performing complex corrective procedures in children. Should children be younger or older? Much could depend on the amount of time after birth that human cardiomyocytes start to lose their fetal characteristics and regenerative potential.
“Mice have this ability to regenerate heart muscle if they are injured for about a week after birth. We have no idea when it stops in humans, and obviously you can’t study this in human babies,” Yutzey explains.
“When the surgeons do these repairs it’s a pretty severe operation. They have to move things around and make connections that didn’t exist before. If there was a way to optimize the growth of new heart muscle after a repair like this, a huge basic question becomes finding out how long the human heart can heal itself after birth.”
Yutzey is part of a wide-ranging collaborative research project with Cincinnati Children’s Heart Institute, including cardiac surgeon Farhan Zafar, MD, and senior research assistant Scott Baker to try and find out. The planned work includes experimental surgical processes dovetailing with detailed laboratory analyses.
“The surgeons tell us that younger infants can do better after having these complex surgeries and there is more plasticity in their hearts and tissues, but none of us have any data on this,” she says.
A long journey ahead
The next phase of the team’s research will involve testing Tbx20 in preclinical models that offer closer comparisons to the human heart.
For its initial work, the team studied mice that were engineered to overexpress Tbx20. Going forward, researchers plan to employ a viral vector to deliver Tbx20 to injured heart tissue. If successful, this approach has more potential for clinical use.
These steps will take time, but at least now, a pathway to that Holy Grail of heart research appears to be open for exploring.
—By Nick Miller
(This article originally appeared in the Summer 2017 issue of Research Horizons)