MedlinePlus Medical Encyclopedia: Familial dysbetalipoproteinemia

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Familial dysbetalipoproteinemia

Contents of this page:
Illustrations Alternative names Definition Causes, incidence, and risk factors Symptoms Signs and tests	Treatment Expectations (prognosis) Complications Calling your health care provider Prevention

Illustrations

Coronary artery disease

Alternative names Return to top

Type III hyperlipoproteinemia; Deficient or defective apolipoprotein E

Definition Return to top

Familial dysbetalipoproteinemia is an inherited disorder in which both cholesterol and triglycerides are elevated in the plasma.

Causes, incidence, and risk factors Return to top

The condition is caused by a gene defect that results in an accumulation of large lipoprotein particles that contain both cholesterol and triglyceride. The disease is inherited in an autosomal recessive manner and can be traced to defects in the gene for apolipoprotein E in many cases. The disease is usually not evident by elevated blood levels or symptoms until the age of 20 or later.

Atherosclerosis develops in the coronary arteries, internal carotid arteries that supply blood to the brain, and the abdominal aorta and its branches. The condition predisposes people to coronary artery disease and peripheral vascular disease.

The condition is worsened by hypothyroidism, obesity, or diabetes. Risk factors are a family history of familial dysbetalipoproteinemia or coronary artery disease.

Symptoms Return to top

Yellow deposits of fatty material in the skin called xanthomas may appear on the palm of the hand, sole of the foot, or on tendons of knees and elbows, and on the eyelids.
There may be early chest pain (angina) or decreased blood flow to other parts of the body, causing transient ischemic attacks of the brain or claudication of the legs.

Signs and tests Return to top

a physical exam revealing characteristic xanthomas
elevated serum LDL
significantly increased remnants of VLDL and chylomicrons
elevated total cholesterol
elevated coronary risk profile triglycerides
increased liklihood of apoE2 genotype
defective apoE protein
atherosclerosis evident by angiogram
abnormal heart stress test

Treatment Return to top

The goal of treatment is to control underlying conditions such as obesity, hypothyroidism, and diabetes that can make dysbetalipoproteinemia appear in people who would otherwise not have it.

The restriction of excess calories and the reduction of saturated fats and cholesterol may significantly reduce cholesterol levels.

If high cholesterol and triglyceride levels persist with maximum dietary treatment, cholesterol lowering agents should be started. Nicotinic acid (niacin), clofibrate, statins or gemfibrozil are drugs that have effectively reduced cholesterol and triglycerides in people affected with dysbetalipoproteinemia.

Expectations (prognosis) Return to top

Individuals with this form of hyperlipidemia have a significantly increased risk for coronary artery disease. With treatment, most people show a significant reduction in lipid levels.

Complications Return to top

premature myocardial infarction (heart tissue death)
strokes
blocked arteries to the body (peripheral vascular disease)
intermittent claudication
gangrene of the lower extremities
xanthomas of the skin

Calling your health care provider Return to top

Call your health care provider if symptoms worsen, do not improve with treatment, or new symptoms develop. Call a genetic counselor if there is a family history of dysbetalipoproteinemia.

Prevention Return to top

Screening for family members of people with familial dysbetalipoproteinemia may lead to early detection and treatment. Early treatment and avoiding other risk factors for vascular disease, such as smoking, are crucial to preventing early heart attacks, strokes and blocked blood vessels.

Update Date: 8/21/2003

Updated by: Douglas R. Stewart, M.D., Division of Medical Genetics, Hospital of the University of Pennsylvania, Philadelphia, PA. Review provided by VeriMed Healthcare Network.

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