Cardiac amyloidosis

• A
• B
• C
• D
• E
• F
• G
• H
• I
• J
• K
• L
• M
• N
• O
• P
• Q
• R
• S
• T
• U
• V
• W
• X
• Y
• Z

Dilated cardiomyopathy

Heart, section through the middle

Cardiac amyloidosis is a disorder caused by deposits of an abnormal protein in the heart tissue, which make it hard for the heart to work properly.

Amyloidosis - cardiac; Primary cardiac amyloidosis - AL type; Secondary cardiac amyloidosis - AA type; Stiff heart syndrome; Senile amyloidosis; Amyloidosis - senile

Amyloidosis is the accumulation of clumps of proteins called amyloids in body tissues and organs. The proteins slowly replace normal tissue. There are many forms of amyloidosis.

Cardiac amyloidosis usually occurs during primary amyloidosis, also called AL type amyloidosis. Primary amyloidosis is usually seen in persons with multiple myeloma, a type of cancer.

Cardiac amyloidosis, also called "stiff heart syndrome," occurs when amyloid deposits take the place of normal heart muscle. It is the most typical type of restrictive cardiomyopathy. Patients with cardiac amyloidosis may have changes in the way electrical signals move through the heart. This is called a conduction disturbance.

Secondary amyloidosis, also called AA type, rarely affects the heart. However, a subtype of secondary amyloidosis called senile amyloidosis involves the heart and blood vessels. Senile amyloidosis is caused by overproduction of a protein different from both the AA and AL types. Senile cardiac amyloidosis is becoming more common as the average age of the population increases.

Cardiac amyloidosis is more common in men than in women. The disease is rare in people under age 40.

Review Date: 01/17/2007
Reviewed By: Larry A. Weinrauch, MD, Assistant Professor of Medicine, Harvard Medical School, and Private practice specializing in Cardiovascular Disease, Watertown, MA. Review provided by VeriMed Healthcare Network.