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Updated: Feb 28, 2026

Isolation and Analysis of Plasma Lipoproteins by Ultracentrifugation
Published on: January 28, 2021
Lipoprotein(a): A missing culprit in the management of athero-thrombosis?
Gianna Ferretti1, Tiziana Bacchetti2, Thomas P Johnston3
1Department of Clinical Sciences (DISCO), Polytechnic University of Marche, Marche, Italy.
Insights
Lipoprotein(a) (Lp(a)) is a key risk factor for heart disease and stroke. Understanding its genetics, metabolism, and measurement is crucial for developing effective therapies to reduce cardiovascular risk.
Area of Science:
- Cardiovascular Science
- Genetics
- Biochemistry
Background:
- Lipoprotein(a) (Lp(a)) is an LDL-like particle independently linked to increased risk of ischemic heart disease, atherosclerosis, thrombosis, and stroke.
- Genetic variations significantly influence plasma Lp(a) levels, impacting its synthesis and metabolism.
- Lp(a) exerts proatherogenic and prothrombotic effects on the vasculature.
Purpose of the Study:
- To review the physicochemical properties and genetic aspects of Lp(a).
- To highlight challenges in accurate Lp(a) quantification and standardization.
- To summarize recent findings on Lp(a) synthesis, metabolism, and its role in atherothrombosis, alongside therapeutic strategies.
Main Methods:
- Literature review focusing on Lp(a) properties, genetics, and metabolism.
- Analysis of pathophysiological mechanisms of Lp(a)-associated atherothrombosis.
- Overview of current and emerging therapeutic interventions targeting Lp(a).
Main Results:
- Lp(a) possesses unique physicochemical properties influencing its atherothrombotic potential.
- Genetic factors are critical determinants of Lp(a) levels and associated cardiovascular risk.
- Standardization of Lp(a) assays remains a challenge due to its polymorphic nature.
Conclusions:
- Accurate Lp(a) determination is essential for risk assessment and management.
- Understanding Lp(a) metabolism and atherothrombotic mechanisms is key to developing targeted therapies.
- Interfering with Lp(a) presents a promising therapeutic avenue for reducing cardiovascular events.
Abstract:
Lipoprotein(a) Lp(a) is a cholesterol-rich, LDL-like particle that is independently associated with an increased risk for ischemic heart disease, atherosclerosis, thrombosis, and stroke. Genetic variation in the Lp(a) locus and some other genes related to Lp(a) synthesis and metabolism play a critical role in regulating plasma Lp(a) levels. The pathophysiological potential of Lp(a) is related to proatherogenic and prothrombotic effects on the vasculature. Different molecular mechanisms underlying the atherothrombotic potential of Lp(a), free apolipoprotein(a), and oxidized-Lp(a) have been proposed. However, plasma Lp(a) assay is complicated by problems associated with quantification and standardization owing to the polymorphic nature of this lipoprotein. This review has focused on the physicochemical properties of Lp(a), the genetic aspects of Lp(a), the need for accurate determination of Lp(a), the synthesis, and recent findings on metabolism of Lp(a). Lastly, the patho-physiological mechanisms by which Lp(a) may increase athero-thrombosis and an overview on the therapeutic modalities to interfere with Lp(a) are summarized.
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