Rare Daily Staff
Researchers led by investigators at Massachusetts General Hospital and the Broad Institute of MIT and Harvard have identified rare DNA variants that substantially increase risk of sudden cardiac death, providing a way to identify people who could benefit from prevention strategies even before exhibiting symptoms.
The findings, presented at the Scientific Sessions of the American Heart Association, were published in the Journal of the American College of Cardiology.
Sudden cardiac death affects 220,000 adults in the United States annually, most of whom have no prior symptoms of a heart issue. The scientists found that the variants they identified that increase risk of sudden cardiac death are present in approximately 1 percent of asymptomatic adults—about 3 million people in the United States.
The authors performed gene sequencing in 600 adult-onset sudden cardiac death cases and 600 controls who remained healthy—the largest such study performed to date and the first to use a control group. A clinical geneticist reviewed all of the DNA variants identified, classifying 15 as clinically important pathogenic variants.
All 15 of these pathogenic variants were in sudden cardiac death cases, with none in controls. The prevalence of a pathogenic variant was found to be 2.5 percent in cases and 0 percent in controls.
The investigators then studied the genes of 4,525 middle-aged adults without any signs of heart disease. They found that 41 (0.9 percent) carried a pathogenic variant. These individuals have been followed for more than 14 years, and those who inherited a pathogenic variant had a more than three-times higher risk of dying from cardiovascular causes.
“In my clinical practice, I often encounter families devastated by a sudden and unexpected death. This finding indicates that genetic testing—if made widely available—can provide a way to identify high-risk individuals currently flying under the radar,” said lead author Amit Khera, cardiologist and associate director of the Precision Medicine Unit at MGH’s Center for Genomic Medicine and the Broad Institute’s Cardiovascular Disease Initiative. “If identified, we have a variety of approaches proven to prevent disease onset available within routine clinical practice.”
Based on these results, Khera and colleagues plan to conduct genetic sequencing tests for thousands of adult patients at MGH and affiliated hospitals who volunteered for a research program designed to understand how genetic and environmental factors impact risk of important diseases. They aim to find the 1 percent of individuals with rare genetic variants linked to heart disease and offer tailored prevention programs in a Cardiovascular Genetics Program or a new MGH Preventive Genomics Clinic that Khera is co-leading and is embedded within primary care.
“Our hope is to empower our patients to better understand, predict, and prevent bad health outcomes,” said Khera, “especially irreversible tragedies such as sudden cardiac death—using genetic information.”
Photo: Amit Khera, cardiologist and associate director of the Precision Medicine Unit at MGH’s Center for Genomic Medicine and the Broad Institute’s Cardiovascular Disease Initiative