Cardiomyopathy can be acquired or inherited. "Acquired" means you aren't born with the disease, but you develop it due to another disease, condition, or factor.
"Inherited" means your parents passed the gene for the disease on to you. Researchers continue to look for the genetic links to cardiomyopathy. They also continue to explore how these links cause or contribute to the various types of the disease.
Many times, the cause of cardiomyopathy isn't known. This often is the case when the disease occurs in children.
The cause of dilated cardiomyopathy often isn't known. As many as one-third of the people who have dilated cardiomyopathy inherit it from their parents.
Certain diseases, conditions, and substances also can cause the disease, such as:
Hypertrophic cardiomyopathy (HCM) usually is inherited. It's caused by a mutation (change) in some of the genes in heart muscle proteins. HCM also can develop over time because of high blood pressure or aging.
Other diseases, such as diabetes or thyroid disease, also can cause HCM. Sometimes the cause of the disease isn't known.
Certain diseases, conditions, and factors can cause restrictive cardiomyopathy, including:
Researchers think that arrhythmogenic right ventricular dysplasia is an inherited disease.
Clinical trials are research studies that explore whether a medical strategy, treatment, or device is safe and effective for humans. To find clinical trials that are currently underway for Cardiomyopathy, visit www.clinicaltrials.gov.
September 3, 2013
Risk factors identified at diagnosis help predict outcomes for children with rare heart condition
A long-term study of children with a complex heart condition called hypertrophic cardiomyopathy (HCM) found that risk factors identified at diagnosis help to predict outcomes for children with this rare condition.
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