Familial Hypercholesterolemia(FH)
by
Rebecca J. Stahl, MA DefinitionFamilial 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. CausesThe 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.
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 heart attacks can occur at a very young age. People with a severe form of this condition usually die at a young age. Risk Factors TOPIf 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. Symptoms TOPFH increases the risk of developing atherosclerosis 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:
Diagnosis TOPThe doctor will ask about your symptoms and medical history. A physical exam will be done. Tests may include:
Treatment TOPOnce 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 ParentIf you or your child has FH from one parent, treatment typically includes: Lifestyle Changes
MedicationBecause 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 ParentsIf you or your child has inherited the gene mutation from both parents, along with cholesterol lowering medications, treatment may also include:
Prevention TOPFH is an inherited condition. It cannot be prevented. RESOURCES:National Heart, Lung, and Blood Institute http://www.nhlbi.nih.gov National Organization for Rare Disorders http://www.rarediseases.org CANADIAN RESOURCES:Canadian Cardiovascular Society http://www.ccs.ca Health Canada http://www.hc-sc.gc.ca References:Familial hypercholesterolemia. EBSCO DynaMed website. Available at: http://www.ebscohost.com/dynamed/what. Updated April 12, 2013. Accessed May 8, 2013.
Genetics Home Reference. Hypercholesterolemia. Genetics Home Reference website. Available at:
http://ghr.nlm.nih.gov/condition=hypercholesterolemia. Updated May 6, 2013. Accessed May 8, 2013.
National Institutes of Health. Familial hypercholesterolemia. National Institutes of Health website. Available at:
http://history.nih.gov/exhibits/genetics/sect2b.htm. Accessed May 8, 2013
National Organization of Rare Disorders. Familial hypercholesterolemia. National Organization of Rare Disorders website. Available at:
http://www.raredis.... Accessed May 8, 2013.
Last reviewed May 2013 by Brian Randall, MD Last Updated: 5/8/2013 |
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