Related Experiment Video
Updated: Dec 12, 2025

Cell-free Biochemical Fluorometric Enzymatic Assay for High-throughput Measurement of Lipid Peroxidation in High Density Lipoprotein
Published on: October 12, 2017
Association of lipoprotein(a) with platelet aggregation and thrombogenicity in patients undergoing percutaneous
Pei Zhu1, Xiao-Fang Tang1, Ying Song1
1Department of Cardiology, State Key Laboratory of Cardiovascular Disease, Fuwai Hospital, National Center for Cardiovascular Diseases, Chinese Academy of Medical Science and Peking Union Medical College, Beijing, China.
Insights
High lipoprotein(a) levels in patients undergoing percutaneous coronary intervention (PCI) are linked to increased platelet aggregation and a higher risk of ischemic events. This suggests lipoprotein(a) may guide the duration of antiplatelet therapy.
Area of Science:
- Cardiovascular Medicine
- Clinical Chemistry
- Hematology
Background:
- Lipoprotein(a) [Lp(a)] is an emerging cardiovascular risk factor.
- Platelet aggregation and thrombogenicity are critical in percutaneous coronary intervention (PCI).
- The role of Lp(a) in platelet function and ischemic outcomes post-PCI requires further elucidation.
Purpose of the Study:
- To assess the association between lipoprotein(a) levels and platelet aggregation/thrombogenicity in PCI patients.
- To investigate the relationship between Lp(a) and ischemic outcomes following PCI.
- To explore Lp(a) as a potential marker for guiding antiplatelet therapy duration.
Main Methods:
- Prospective study of 6601 consecutive patients undergoing PCI on dual antiplatelet therapy.
- Measurement of lipoprotein(a) levels and modified thrombelastography (including platelet mapping).
- Two-year follow-up for major adverse cardiovascular and cerebrovascular events using Cox proportional regression analysis.
Main Results:
- Higher Lp(a) levels correlated with accelerated fibrin generation and increased clot strength.
- Patients with higher Lp(a) showed significantly greater adenosine diphosphate (ADP)-induced platelet aggregation.
- Elevated Lp(a) was associated with a 16% increased risk of major adverse cardiovascular and cerebrovascular events post-PCI, persisting after risk factor adjustment.
Conclusions:
- High plasma Lp(a) levels are associated with enhanced platelet aggregation and thrombogenicity in PCI patients.
- Elevated Lp(a) predicts a higher risk of ischemic events after PCI.
- Lp(a) may serve as a biomarker to identify patients who could benefit from prolonged antiplatelet therapy.
Abstract:
This study aimed to evaluate the association of lipoprotein(a) levels with platelet aggregation and thrombogenicity in patients undergoing percutaneous coronary intervention (PCI), and to investigate the ischemic outcome on this population. Lipoprotein(a) and modified thrombelastography were measured in 6601 consecutive patients underwent PCI on dual antiplatelet therapy. Cox proportional regression analysis was applied to illustrate the ischemic events in a 2-year follow up. The mean levels of lipoprotein(a) were 29.0 mg/dl. Patients with higher lipoprotein(a) levels had significantly accelerated fibrin generation (lower K time and bigger α angle) and greater clot strength (higher maximum amplitude (MA)) than patients with lower lipoprotein(a) levels (P < .001). Moreover, the higher lipoprotein(a) group also exhibited significantly higher adenosine diphosphate (ADP) induced platelet aggregation (MAADP) by thrombelastography platelet mapping assay than lower lipoprotein(a) group. Cox regression analyzes revealed that patients with higher lipoprotein(a) levels had a 16% higher risk of major adverse cardiovascular and cerebrovascular events (HR 1.159, 95%CI: 1.005-1.337, P = .042) compared with patients with lower lipoprotein(a) levels. This association persisted after adjustment for a broad spectrum of risk factors (HR 1.174, 95%CI: 1.017-1.355, P = .028). High plasma lipoprotein(a) levels were associated with increased platelet aggregation and ischemic events in patients underwent PCI. Lipoprotein(a) might indicate the need for prolonged antiplatelet therapy.
Related Concept Videos
Antiplatelet Drugs: Prostaglandin Synthesis, P2Y12 and Glycoprotein IIb/IIIa Inhibitors
Prostaglandin synthesis inhibitors, exemplified by the widely known aspirin, wield their power by irreversibly acetylating...
Peripheral Artery Disease I: Introduction
Atherosclerosis I: Introduction
Coronary Artery Disease II: Pathophysiology
Peripheral Artery Disease III: Interprofessional Care
Acute Coronary Syndrome II: Pathophysiology and Clinical Manifestations

