Learning About Cardiac Amyloidosis
What is it?

Cardiac amyloidosis is a buildup of abnormal protein (called amyloid) in the heart muscle. Over time, the
heart muscle may become stiff and cannot expand to let enough blood enter its chambers. Your heart may not be
able to pump enough blood to meet your body's needs. There are different types of amyloidosis.
What causes it?
Many diseases can lead to cardiac amyloidosis. Sometimes the cause is not known. Other times, it can run in
families (inherited). It may be part of the changes that happen with aging.
What are the symptoms?
You may not have symptoms at first. Or you may have symptoms such as:
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Feeling very tired.
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Feeling weak.
If your heart gets weaker, you may develop heart failure. If this happens, you may have other symptoms. These
include:
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Shortness of breath, especially with activity.
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Trouble breathing when you lie down.
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Fainting.
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Swelling in your legs or belly.
If you have amyloidosis in other parts of your body, you may have other symptoms.
How is it diagnosed?
Your doctor will do a physical exam and ask about your symptoms. You may have an electrocardiogram (EKG),
echocardiogram, and MRI scan of your heart. You may need other imaging tests. Blood and urine tests may be
done. You may have genetic testing. In some cases, a heart tissue biopsy may be done.
How is it treated?
How cardiac amyloidosis is treated depends on your symptoms and what's causing the condition. The goal is to
feel better, prevent other problems, and slow down the disease.
You may be treated with medicines to help get rid of extra fluid. Extra fluid causes swelling and makes it
hard to breathe. You may need blood thinners to prevent a stroke and other problems.
Your doctor may talk with you about other medicines, treatments, and procedures to help you stay healthier
and live longer.
Current as of: June 27, 2023
Content Version: 14.0
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