What is cardiomyopathy?
Any disorder that affects the heart muscle is called a cardiomyopathy. Cardiomyopathy
causes the heart to lose its ability to pump blood well. In some cases, the heart
rhythm also becomes disturbed. This leads to arrhythmias (irregular heartbeats). There
are many causes of cardiomyopathy, including:
High blood pressure
Coronary artery disease
Often, the exact cause of the muscle disease is never found.
How does cardiomyopathy differ from other heart disorders?
Cardiomyopathy differs from many of the other disorders of the heart in several ways,
Cardiomyopathy can occur in young people.
The condition tends to be progressive. Sometimes it worsens fairly quickly.
It may be associated with diseases involving other organs, as well as the heart.
Dilated cardiomyopathy is a leading cause for a heart transplant.
It is often the result of gradual changes of heart structure over time
What causes cardiomyopathy?
Viral infections in the heart are a major cause of cardiomyopathy. In some cases,
another disease or its treatment causes cardiomyopathy. This might include complex
congenital (present at birth) heart disease, nutritional deficiencies, uncontrollable,
fast heart rhythms, or certain types of chemotherapy for cancer. Sometimes, cardiomyopathy
can be linked to a genetic defect. Other times, the cause is unknown. Three types
of cardiomyopathy typically affect adults. They are:
What is hypertrophic cardiomyopathy?
Hypertrophic cardiomyopathy occurs when the muscle of the left ventricle thickens.
This can block blood flow to the rest of the body. Hypertrophic cardiomyopathy can
affect the heart's mitral valve, causing blood to leak backward through the valve.
This is a rare disease and in most cases is inherited.
It can affect men and women of all ages. Symptoms can appear in childhood or adulthood.
Symptoms include shortness of breath on exertion, dizziness, fainting, and chest pain
Some people have arrhythmias, which may lead to sudden death.
What is dilated cardiomyopathy?
Dilated cardiomyopathy is the most frequent form of cardiomyopathy. The cavity of
the heart is enlarged and stretched, compromising the heart's ability to pump normally
and relax appropriately:
This occurs most often in adults ages 20 to 60. It is more common in men than women,
but has been diagnosed in people of all ages, including children.
Most people eventually develop heart failure.
Dilated cardiomyopathy can be caused by chronic, heavy alcohol use and nutritional
deficiencies tied to alcoholism.
It sometimes occurs as a complication of pregnancy and childbirth.
Other possible causes include: alcohol abuse, infections, and illicit drugs. Rarely,
it is inherited. Sometimes medicines used to treat a different medical condition can
damage the heart and cause dilated cardiomyopathy. However, in most cases, a specific
cause is never found.
What is restrictive cardiomyopathy?
Restrictive cardiomyopathy occurs when the heart muscle becomes stiff and not able
to fill with blood properly. It's the least common type of cardiomyopathy in the U.S.
It often occurs due to an underlying problem, such as amyloidosis, hemochromatosis,
scleroderma, or sarcoidosis.
Restrictive cardiomyopathy does not appear to be inherited, but some of the diseases
that lead to the condition are inherited.
Symptoms may include fatigue, swelling of the arms and legs, and trouble breathing
What is arrhythmogenic right ventricular dysplasia?
ARVD is a rare type of cardiomyopathy that occurs if the muscle tissue in the right
ventricle dies and is replaced by fat or scar tissue:
This process disrupts the heart's electrical system, causing arrhythmias.
It usually affects teens and young adults.
Symptoms include heart palpitations and fainting after physical activity.
It can cause sudden cardiac arrest in young athletes.
It may require implantation of a device to prevent death from an arrhythmia