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Elevated lipoprotein(a) (Lp[a]) represents the most common type of genetic dyslipidemia.1 Elevated Lp(a) levels occurring in 20% of the general population, particularly in certain races and ethnicities.2 More than 70 million people in North America and 1.5 billion people globally are affected.2,3
Lp(a) is the only apo(a)-containing lipoprotein.4 Elevated Lp(a) is an independent, genetic, and causal risk driver of atherosclerotic cardiovascular disease (ASCVD).1,3-5 Elevated Lp(a) levels remain a risk driver for ASCVD development even when plasma low- density lipoprotein cholesterol (LDL-C) levels have been reduced.4 Moreover, patients with elevated Lp(a) levels likely have family members with elevated levels.6,7 Elevated Lp(a) is also an independent predictor of premature ASCVD. US and global consensus statements and guidelines for Lp(a) recommend various patient types be screened/tested for elevated Lp(a).1,6-10 In 2018, two International Statistical Classification of Diseases, Tenth Revision (ICD-10) codes to justify Lp(a) testing were added: E78.41, Elevated Lp(a); and Z83.430, Family history of elevated Lp(a).6,11
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