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Lipoprotein(a) is a blood lipid particle that is largely determined by genetics and can significantly increase the risk of cardiovascular disease.
Regular tips about health Regular tips about health Add as Preferred SourceLipoprotein(a) is a blood lipid particle that is largely determined by genetics and can significantly increase the risk of cardiovascular disease.
Lipoprotein(a), commonly abbreviated as Lp(a), is a unique lipoprotein particle found in the blood. It consists of an LDL-like core particle bound to an additional protein called apolipoprotein(a). Lp(a) is considered an independent risk factor for cardiovascular disease and its blood concentration is largely determined by genetics -- diet and lifestyle have minimal influence on its levels.
More than 90% of the variation in Lp(a) levels is genetically determined and can differ significantly between populations. Some factors that may influence levels include:
Elevated Lp(a) promotes the development of atherosclerosis (hardening and narrowing of the arteries) and simultaneously impairs the natural breakdown of blood clots (fibrinolysis), because apolipoprotein(a) structurally resembles plasminogen, a key protein in clot dissolution. This dual mechanism raises the risk of:
Lp(a) levels are measured through a standard blood test. Current guidelines recommend at least one measurement during a lifetime, particularly for individuals with:
An Lp(a) level below 30 mg/dl (or below 75 nmol/l) is generally considered normal. Values above 50 mg/dl are considered significantly elevated and are associated with a substantially increased cardiac risk.
Directly lowering Lp(a) with medication has historically been challenging, as conventional lipid-lowering drugs such as statins have little effect on Lp(a) levels. Current and emerging treatment options include:
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