Hypertriglyceridemia (patient information)

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Hypertriglyceridemia (patient information)
Overview
What are the symptoms?
What are the causes?
Who is at highest risk?
When to seek urgent medical care?
Diagnosis
Treatment options
Where to find medical care for Hypertriglyceridemia (patient information)?
What to expect (Outlook/Prognosis)?
Possible complications
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-In-Chief: Priyamvada Singh, M.B.B.S. [2]

Overview

Familial hypertriglyceridemia is a common disorder passed down through families in which the level of triglycerides (a type of fat) in a person's blood are higher than normal. The condition is not associated with a significant increase in cholesterol levels.

What are the symptoms of Hypertriglyceridemia?

You may not notice any symptoms. People with the condition may have coronary artery disease at an early age.

What causes Hypertriglyceridemia?

Familial hypertriglyceridemia is caused by a genetic defect, which is passed on in an autosomal dominant fashion. This means that if you get a bad copy of the gene from just one of your parents, you will have the condition. Some people with this condition also have high levels of very low density lipoprotein (VLDL). The reason for the rise in triglycerides and VLDL is not understood. Familial hypertriglyceridemia does not usually become noticeable until puberty or early adulthood. Obesity, hyperglycemia (high blood glucose levels), and high levels of insulin are often also present and may cause even higher triglyceride levels. Familial hypertriglyceridemia occurs in about 1 in 500 individuals in the United States. Risk factors are a family history of hypertriglyceridemia or a family history of heart disease before the age of 50.

Who is at highest risk?

Family members with history of hypertriglyceridemia are at increased risk of having the condition.

When to seek urgent medical care?

You may not notice any symptoms. People with the condition may have coronary artery disease at an early age.

Diagnosis

People with a family history of this condition should have blood tests to check very low density lipoprotein (VLDL) and triglyceride levels. Blood tests usually show a mild to moderate increase in triglycerides (about 200 to 500 mg/dL). A coronary risk profile may also be done.

Treatment options

The goal of treatment is to control conditions that can raise triglyceride levels such as obesity, hypothyroidism, and diabetes. Your doctor may tell you not to drink alcohol. Because certain birth control pills can raise triglyceride levels, you should carefully discuss their use with your doctor. Treatment also involves avoiding excess calories and foods high in saturated fats and carbohydrates. See also: Heart disease and diet If high triglyceride levels persist despite diet changes, medication may be needed. Nicotinic acid, gemfibrozil (Lopid), and fenofibrate have been shown to lower triglyceride levels in people with this condition.

Where to find medical care for Hypertriglyceridemia?

Directions to Hospitals Treating Hypertriglyceridemia

What to expect (Outlook/Prognosis)?

Persons with this condition have an increased risk of coronary artery disease and pancreatitis. Losing weight and keeping diabetes under control helps improve the outcome.

Possible complications

• Pancreatitis
• Coronary artery disease

Prevention

Screening family members for high triglycerides may detect the disease early.

Sources

http://www.nlm.nih.gov/medlineplus/ency/article/000397.htm Template:WS Template:WH