Lipoprotein(a): A Genetically Determined, Causal, and Prevalent Risk Factor for Atherosclerotic Cardiovascular Disease. Issue 1 (January 2022)

• Record Type: Journal Article
• Authors: Reyes-Soffer, Gissette; Ginsberg, Henry N.; Berglund, Lars; Duell, P. Barton; Heffron, Sean P.; Kamstrup, Pia R.; Lloyd-Jones, Donald M.; Marcovina, Santica M.; Yeang, Calvin; Koschinsky, Marlys L.
• Is Part Of: Arteriosclerosis, thrombosis, and vascular biology. Volume 42:Issue 1(2022)
• Publication Date: 2022-01
• Subjects: AHA Scientific Statements -- apolipoprotein B100 -- atherosclerotic cardiovascular disease -- cholesterol, low-density lipoprotein -- lipoprotein(a); Arteriosclerosis -- Periodicals; Thrombosis -- Periodicals; Blood-vessels -- Pathophysiology -- Periodicals; Electronic journals; 616.13
• DOI: 10.1161/ATV.0000000000000147
• Languages: English
• ISSNs: 1079-5642

Abstract

Abstract : High levels of lipoprotein(a) [Lp(a)], an apoB100-containing lipoprotein, are an independent and causal risk factor for atherosclerotic cardiovascular diseases through mechanisms associated with increased atherogenesis, inflammation, and thrombosis. Lp(a) is predominantly a monogenic cardiovascular risk determinant, with ≈70% to ≥90% of interindividual heterogeneity in levels being genetically determined. The 2 major protein components of Lp(a) particles are apoB100 and apolipoprotein(a). Lp(a) remains a risk factor for cardiovascular disease development even in the setting of effective reduction of plasma low-density lipoprotein cholesterol and apoB100. Despite its demonstrated contribution to atherosclerotic cardiovascular disease burden, we presently lack standardization and harmonization of assays, universal guidelines for diagnosing and providing risk assessment, and targeted treatments to lower Lp(a). There is a clinical need to understand the genetic and biological basis for variation in Lp(a) levels and its relationship to disease in different ancestry groups. This scientific statement capitalizes on the expertise of a diverse basic science and clinical workgroup to highlight the history, biology, pathophysiology, and emerging clinical evidence in the Lp(a) field. Herein, we address key knowledge gaps and future directions required to mitigate the atherosclerotic cardiovascular disease risk attributable to elevated Lp(a) levels.