Gene
abnormalities may make some people more susceptible to myocarditis, a
rare type of heart inflammation that can affect young people and
athletes, a large new study shows.
The findings, published Monday in the American Heart Association journal Circulation,
could partially answer why otherwise healthy young people sometimes
develop a condition that can lead to heart failure and sudden cardiac
death, researchers said.
In the rare instances when it happens,
myocarditis "often affects young patients in the prime of life, and
we've never understood why," said senior study author Dr. Sanjay Prasad,
a professor of cardiomyopathy at the Imperial College London in the
United Kingdom. He also is a consultant cardiologist at Royal Brompton
Hospital in London.
The new, population-based study suggests that
"it's not just random," he said. "For a subset of people, there's a
gene that predisposes them to this, or makes them susceptible."
Myocarditis,
an inflammation of the heart, frequently is triggered by a virus. The
condition can progress to heart muscle disease that weakens the heart
and its ability to pump blood. Myocarditis usually resolves on its own
or with treatment, but in some cases it can cause lasting damage. It
also can be fatal.
Previously undetected and untreated
myocarditis has been identified as the cause of sudden death in 8% of 1-
to 17-year-olds and 9% of athletes. Postmortem studies suggest it may
be responsible for 3% to 12% of all sudden cardiac deaths.
Studies
have found a small but increased risk of myocarditis following COVID-19
infection and an even smaller, but still elevated, risk after COVID-19
vaccination.
The new research involved two types of heart muscle
disease associated with myocarditis. Dilated cardiomyopathy, the most
common type, typically affects adults under age 50. It occurs when the
heart muscle dilates, becoming thin and enlarging the heart's chambers,
making blood pumping more difficult. In arrhythmogenic cardiomyopathy,
heart muscle is replaced by scarring and fat, causing changes in heart
rhythms.
Researchers analyzed DNA sequencing data for 336 people
with acute myocarditis and 1,053 healthy people in the U.K. and the
Netherlands, looking for genetic variants associated with the two types
of cardiomyopathy. Both groups were predominantly men.
The
participants were followed for five years. Among those who had
myocarditis, 8% – or 1 in 13 – had genetic variants associated with the
cardiomyopathies, compared with fewer than 1% of those without
myocarditis.
While this data was collected between 2016 and 2018,
prior to the COVID-19 pandemic, Prasad said others are now studying
whether a subset of people with COVID-19-related myocarditis or COVID-19
vaccine-related myocarditis also had these genetic variants.
If supported by other studies, the findings could impact care for people with myocarditis and their families, the authors said.
"These
findings suggest there should be a low threshold for genetic testing in
patients who present with myocarditis – particularly when there isn't
an obvious reason for it," said Dr. Amrit Lota, the study's lead author
and a consultant cardiologist at Royal Brompton Hospital.
People
with a family history of myocarditis or cardiomyopathy – along with
young patients with poor heart function, frequent heart rhythm
disturbances or who have a lot of scarring on heart MRIs – also should
be considered for testing, he said.
Dr. Adam Helms, a
cardiologist and assistant professor at the University of Michigan
Frankel Cardiovascular Center in Ann Arbor, said he routinely conducts
genetic testing on patients with myocarditis for his research and was
not surprised to see genetic variants associated with the condition.
Helms was not involved in the new study.
"What this study did was
they found it to be true in a very large cohort," he said. "This
presents a strong case for genetic testing."
Knowing someone has a genetic variant associated with myocarditis could affect the type of treatment provided, he said.
"Sometimes
cases of myocarditis are treated with immunosuppression," Helms said.
"But this is not the best way to treat hereditary cases. There are no
studies to suggest those cases would improve."
Medications such
as beta blockers might be more effective for people genetically
predisposed to myocarditis, Helms said, because they may have a higher
risk of future heart problems, such as heart failure.
Prasad said
his team was continuing to follow the people in this study – as well as
expanding it to include more patients – to find out how those with the
genetic variants fared over the long term. Future investigations also
would analyze data across ethnicities and gender to look for differences
among specific groups.