Elevated high-density lipoprotein (HDL) level is abnormally high levels of HDL cholesterol in the blood.
(See also Overview of Cholesterol and Lipid Disorders.)
A high level of HDL cholesterol (the "good" cholesterol) may decrease the risk of heart attacks and strokes. However, HDL cholesterol levels may be increased in some genetic disorders. In these disorders, the high HDL level may not protect against heart attacks or strokes, probably because the disease also causes other changes in lipid levels and other abnormalities in the way the body breaks down food.
Elevated HDL levels may be
Primary: Caused by a genetic mutation
Secondary: Caused by another disorder
Primary causes of elevated HDL levels are
Genetic mutations that result in overproduction or decreased removal of HDL
Secondary causes of high HDL cholesterol include all of the following:
Alcohol use disorder without cirrhosis
An overactive thyroid gland (hyperthyroidism)
Medications (for example, corticosteroids, insulin, phenytoin) Medications (for example, corticosteroids, insulin, phenytoin)
A disorder that is causing very high HDL levels is treated.
Cholesteryl ester transfer protein (CETP) deficiency
Cholesteryl ester transfer protein (CETP) deficiency is a rare autosomal recessive disorder caused by a mutation of the CETP gene. Because CETP helps in the transfer of cholesterol from HDL to other lipoproteins, CETP deficiency affects low-density lipoprotein (LDL) cholesterol levels and slows removal of HDL cholesterol from the blood. Affected people have no symptoms but have high HDL cholesterol in their blood. No treatment is necessary.
Familial hyperalphalipoproteinemia
Familial hyperalphalipoproteinemia is an autosomal dominant disorder caused by various genetic mutations. The disorder is usually diagnosed when elevated HDL cholesterol levels are found during a routine blood test. Affected people have no symptoms. No treatment is necessary.
