| Risk Factors
Familial hypercholesterolemia (FH) is an inherited condition. It causes
high levels of total cholesterol. It also increases levels of low density lipoprotein (LDL), or bad cholesterol. These high cholesterol levels increase a person’s risk for developing heart disease.
The liver removes LDL cholesterol from the blood. It does this by making receptors that attach to LDL cholesterol. With FH, there are problems with the receptors. There may be too few receptors, or they may not work as they should.
The Liver and Other Organs
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These problems are caused by a gene mutation. FH may be inherited from one or both parents.
If inherited from both parents, the condition is severe. Heart disease and
can occur at a very young age. People with a severe form of this condition usually die at a young age.
If one of your parents has the gene mutation for FH, you are at higher risk for the condition. If both your parents have the gene mutation, you have an even higher chance of having the condition.
FH increases the risk of developing
at a young age. This is the hardening of arteries from plaque build-up. This can lead to:
The build-up of plaque can also cause:
Thick and painful tendons, especially the
Xanthomas—fatty deposits beneath the skin most commonly found on the elbows, joints, tendons, knees, hands, feet, and buttocks
Xanthelasmas—fatty deposits on the eyelids
- Eye problems—fatty deposits on the cornea
The doctor will ask about your symptoms and medical history. A physical exam will be done.
Tests may include:
- Blood tests for cholesterol levels
- Heart function tests
- Genetic testing to look for the gene mutation
Once the diagnosis is made, you or your child will need life-long treatment. The main treatment goal is lower you or your child's risk of developing heart disease, strokes or other problems from atherosclerosis. This can be done not only by lowering your cholesterol levels, but also by decreasing other risk factors for developing heart disease. The doctor may recommend that you or your child work with a lipid specialist.
Treatment for FH Inherited From One Parent
If you or your child has FH from one parent, treatment typically includes:
- Alow-fat, low-cholesterol diet
may be recommended. You may need to work with a dietitian.
is very important. Talk to the doctor before starting an exercise program.
- If you smoke, talk to the doctor about programs to help you quit.
- Maintaining a healthy weight is important.
If you are overweight,
talk to the doctor about how to lose weight.
- Make sure other medical conditions such as high blood pressure and diabetes are being treated and controlled.
Because FH is an inherited condition, diet and exercise is often not enough to lower high cholesterol levels. In most cases, cholesterol-lowering medications called statins are prescribed for both children and adults. Statins may be able to reduce the risk of heart disease and death. In some cases, other cholesterol-lowering medications are also prescribed.
These medications are best used as additions to diet and exercise and should not replace healthy lifestyle changes.
Treatment for FH Inherited From Both Parents
If you or your child has inherited the gene mutation from both parents, along with cholesterol lowering medications, treatment may also include:
- Apheresis—a process that uses a special machine to filter LDL from the blood
Liver transplant—may be done in severe cases where the condition is getting worse and treatment has been unsuccessful
FH is an inherited condition. It cannot be prevented.