Elevated lipoprotein(a) (Lp[a]) represents the most common type of genetic dyslipidemia.1 High Lp(a) values may occur in 20% of the general population and more frequently in certain races and ethnicities.2 More than 70 million people in North America and 1.5 billion individuals globally are affected.2,3
Lp(a) is an apoB family lipoprotein.4 Elevated Lp(a) concentration is an independent, genetic, and causal risk driver of atherosclerotic cardiovascular disease (ASCVD).1,3-5 High Lp(a) levels remain a risk factor for ASCVD development even when plasma low-density lipoprotein cholesterol (LDL-C) levels have been reduced.4 Moreover, patients with high Lp(a) levels likely have family members with high levels, too.6,7 US and Global consensus statements and guidelines related to Lp(a) recommend various patient types be screened/tested for elevated Lp(a).1,6-10 In 2018, two International Classification of Diseases-10 (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