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Apo(a) protein size ranges from 300 to 800 kDa, driving Lp(a) extreme variability, a review of this elusive risk factor (Arterioscler Thromb Vasc Biol 2004)

Original title: Lipoprotein(a): an elusive cardiovascular risk factor

Arterioscler Thromb Vasc Biol · · 6

Berglund L, Ramakrishnan R

This review by Berglund and Ramakrishnan examines Lp(a), a lipoprotein found only in humans, Old World primates, and the European hedgehog, resembling LDL but containing the unique, structurally distinct protein apo(a). Variability in the apo(a) gene size produces a protein molecular weight ranging from 300 to 800 kDa, likely reflecting neutral evolution without selective advantage, and this size polymorphism drives much of Lp(a) heterogeneity, with an inverse but complex relationship between apo(a) size and Lp(a) levels; Lp(a) levels also vary between populations, with Black individuals generally having higher levels than Asian or white individuals adjusting for apo(a) size, and an upstream pentanucleotide repeat further affecting levels. Multiple meta-analyses support an association between Lp(a) and coronary artery disease, particularly for Lp(a) carried in smaller apo(a) isoforms, and Lp(a) interacts with other cardiovascular risk factors, though its underlying physiological role remains unknown.

Read the paper (DOI)PubMed

Original abstract

Lipoprotein (a) [Lp(a)], is present only in humans, Old World nonhuman primates, and the European hedgehog. Lp(a) has many properties in common with low-density lipoprotein (LDL) but contains a unique protein, apo(a), which is structurally different from other apolipoproteins. The size of the apo(a) gene is highly variable, resulting in the protein molecular weight ranging from 300 to 800 kDa; this large variation may be caused by neutral evolution in the absence of any selection advantage. Apo(a) influences to a major extent metabolic and physicochemical properties of Lp(a), and the size polymorphism of the apo(a) gene contributes to the pronounced heterogeneity of Lp(a). There is an inverse relationship between apo(a) size and Lp(a) levels; however, this pattern is complex. For a given apo(a) size, there is a considerable variation in Lp(a) levels across individuals, underscoring the importance to assess allele-specific Lp(a) levels. Further, Lp(a) levels differ between populations, and blacks have generally higher levels than Asians and whites, adjusting for apo(a) sizes. In addition to the apo(a) size polymorphism, an upstream pentanucleotide repeat (TTTTA(n)) affects Lp(a) levels. Several meta-analyses have provided support for an association between Lp(a) and coronary artery disease, and the levels of Lp(a) carried in particles with smaller size apo(a) isoforms are associated with cardiovascular disease or with preclinical vascular changes. Further, there is an interaction between Lp(a) and other risk factors for cardiovascular disease. The physiological role of Lp(a) is unknown, although a majority of studies implicate Lp(a) as a risk factor.

ancestrygenetics

Summary written by lp-a.org from the published abstract; figures as published. Page updated 18 August 2026. Methods.