An infant born with a relatively simple heart defect is far more likely to develop heart problems as an adult, researchers at the Stanford University School of Medicine have discovered.
The risk is so great that someone born with a heart defect who has a heart-healthy lifestyle is twice as likely to develop heart problems as someone born without a defect who has a heart-averse lifestyle.
“All of us in cardiology recognize that people with complex disease need follow-up care throughout their lives,” said James Priest, MD, assistant professor of pediatric cardiology. “But for the simple problems, we’ve been thinking that once you close the hole or fix the valve, these patients are good to go.”
The research findings suggest that the medical community should watch adults who were born with heart defects — even minor ones — more carefully. Medications and lifestyle changes may help prevent or delay major heart conditions, such as heart attacks, stroke, heart failure and atrial fibrillation.
A paper describing the research will be published Feb. 28 in Circulation. Priest is the senior author; Priyanka Saha, a student at Harvard Medical School who was a research fellow at Stanford from 2017 to 2018, is the lead author.
Most common congenital condition
About 1 percent of infants are born with heart defects, the most common congenital condition. Those with less-complex defects, such as a hole in the heart or a faulty valve, nearly always survive into adulthood, sometimes unaware of the defect until later in life.
To conduct their research, Priest, Saha and their colleagues mined data from the U.K. Biobank, which includes health data on 500,000 British residents aged 37 to 73 during the biobank’s recruitment period from 2006 to 2010. They found 2,006 people who had mild congenital heart defects.
For reasons the researchers don’t understand, the members of this group were slightly more likely to be obese, to smoke, to have high blood pressure and to have diabetes — all factors that increase the risk for cardiovascular problems.
However, even after adjusting for those risk factors, they found that those born with mild heart defects were 13 times as likely to develop heart failure or atrial fibrillation, five times as likely to have a stroke, and twice as likely to suffer a heart attack than those born without heart defects.
Adult survivors of congenital heart defects with fewer risk factors for heart disease — such as smoking, having high blood pressure and being obese — fared better than those who had more risk factors. Those with a heart-healthy lifestyle were about a third less likely to develop heart conditions than those with five or more heart disease risk factors.
A mystery
It’s unclear why adults who were born with heart defects suffer more heart disease, the study said. The researchers propose several possibilities, including the stress of surgery, genetic predisposition and cellular dysfunction.
“Is it the surgery? Could it be the medications? Or is it something intrinsic to having congenital heart disease? We don’t know,” Priest said, adding, “We don’t know why infants have congenital heart disease to begin with.”
Saha said further research into why congenital heart disease leads to adult heart problems could help shape follow-up care. But physicians can begin helping these patients right away by providing more surveillance.
“That’s something that can change right now,” she said. “We can start connecting them with cardiology specialists.”
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Other Stanford co-authors of the study are Praneetha Potiny, life sciences research assistant; Joseph Rigdon, PhD, research engineer; Melissa Morello, MD, fellow in adult congenital heart disease; Catherine Tcheandjieu, PhD, DVM, postdoctoral scholar; Anitra Romfh, MD, clinical assistant professor of pediatric cardiology; Susan Fernandes, LPD, PA-C, clinical professor of pediatric cardiology; Doff McElhinney, MD, professor of cardiothoracic surgery; Daniel Bernstein, MD, professor of pediatric cardiology; George Lui, MD, clinical associate professor of cardiovascular medicine; Gary Shaw, DrPH, professor of pediatrics; and Erik Ingelsson, MD, PhD, professor of cardiovascular medicine.
Priest is a member of the Stanford Cardiovascular Institute, the Stanford Maternal & Child Health Research Institute and the Wu Tsai Neurosciences Institute at Stanford.
The work was funded by the National Institutes of Health (grant K99HL130523) and the Sarnoff Cardiovascular Research Foundation.
Stanford’s departments of Pediatrics and of Cardiothoracic Surgery also supported the work.
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