NEW DRUG, POSITIVE RESULTS FOR HYPERTROPHIC CARDIOMYOPATHY

NEW DRUG, POSITIVE RESULTS FOR HYPERTROPHIC CARDIOMYOPATHY (Links to an external site)

An estimated 1 million people in the U.S. have hypertrophic cardiomyopathy—a heart condition also known as HCM—and many don’t know they have the condition until it’s too late. A genetic disease, HCM often goes undetected until someone in the family experiences symptoms, which can range from irregular heart rhythms and stroke to heart failure and death in people of any age. And HCM is the most common cause of sudden cardiac death in young people.

Genetic testing can identify immediate family at risk of HCM (Links to an external site)

As an inherited disease, HCM can run in families—and it can develop at any age. In many instances, HCM is undiagnosed until a significant heart problem occurs. When that happens, genetic testing for the patient and the immediate family can help to clarify the cause of symptoms and offer care options for others in the family who may be at risk. Screening often includes an echocardiogram and genetic testing.
Cresci spearheads precision medicine statement for heart failure

Cresci spearheads precision medicine statement for heart failure (Links to an external site)

Sharon Cresci, MD, an associate professor of medicine and of genetics in the Cardiovascular Division at Washington University School of Medicine in St. Louis, led a committee that developed the American Heart Association’s (AHA) scientific statement on the potential for precision medicine to improve treatment for patients with heart failure.