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Published on: November 10, 2017
Effect of specific lipoprotein(a) apheresis on coronary atherosclerosis regression assessed by quantitative coronary
Maya S Safarova1, Marat V Ezhov, Olga I Afanasieva
1Cardiology Research Center 15A, 3rd Cherepkovskaya Street, 121552 Moscow, Russia. Dr.Safarova@gmail.com
Insights
Specific lipoprotein(a) [Lp(a)] apheresis significantly reduced coronary atherosclerosis in patients with coronary heart disease. This Lp(a) lowering therapy demonstrated greater efficacy than atorvastatin alone.
Area of Science:
- Cardiology
- Vascular Biology
- Lipid Metabolism
Background:
- Elevated lipoprotein(a) [Lp(a)] is a risk factor for coronary heart disease (CHD).
- Specific Lp(a) apheresis aims to reduce cardiovascular events by lowering Lp(a) levels.
Purpose of the Study:
- To evaluate the impact of specific Lp(a) apheresis on coronary atherosclerosis progression.
- To compare the efficacy of Lp(a) apheresis versus atorvastatin in CHD patients with elevated Lp(a).
Main Methods:
- Prospective study of 30 CHD patients with elevated Lp(a) and LDL-C on statins.
- Randomized allocation to weekly Lp(a) apheresis (n=15) or atorvastatin only (n=15) for 18 months.
- Quantitative coronary angiography assessed percent diameter stenosis and minimal lumen diameter (MLD).
Main Results:
- Lp(a) apheresis reduced Lp(a) by 73% and Lp(a)-corrected LDL-C by 7%.
- Median percent diameter stenosis decreased with apheresis (-2.0%) versus increased with atorvastatin (3.5%).
- Apheresis showed a more favorable effect on MLD (0.20 mm vs 0.01 mm) and higher rates of coronary segment regression/stabilization.
Conclusions:
- Specific Lp(a) apheresis promotes coronary atherosclerosis regression in stable CHD patients.
- This apheresis therapy effectively lowers Lp(a) and helps achieve LDL-C goals.
- Lp(a) apheresis is a promising therapeutic option for managing high Lp(a) in CHD.
Aim:
To evaluate the effect of specific lipoprotein(a) [Lp(a)] apheresis on coronary atherosclerosis progression in coronary heart disease (CHD) patients with elevated Lp(a) levels.
Methods:
A total of 30 subjects (mean age 53.5 ± 8.3 years, 70% male) with CHD verified by angiography, Lp(a) > 50 mg/dL, and low density lipoprotein cholesterol (LDL-C) ≤ 2.5 mmol/L on chronic statin treatment were prospectively evaluated for 18 months. Patients were allocated to receive specific Lp(a) apheresis, which was carried out weekly with Lp(a) Lipopak(®) columns (POCARD Ltd., Russia) (n = 15), or atorvastatin only (n = 15). Blinded quantitative coronary angiography analyses of percent diameter stenosis and minimal lumen diameter (MLD) were performed at baseline and after the 18-month treatment period.
Results:
By the single specific Lp(a) apheresis procedure, Lp(a) level decreased by an average of 73 ± 12% to a mean of 29 ± 16 mg/dL, and mean Lp(a)-corrected LDL-C decreased by 7% to a mean of 1.4 mmol/L. Median percent diameter stenosis was reduced by -2.0 (95% confidence interval [CI], -5.0-0.0) with apheresis (p < 0.01 in comparison with baseline), and increased by 3.5 (0.0-6.9) with atorvastatin (p < 0.001 between the groups). The effect on MLD was more favorable with apheresis than with atorvastatin: 0.20 ± 0.39 mm, as compared with 0.01 ± 0.34 mm, p = 0.04. Lp(a) apheresis had greater efficacy regarding the amount of regressed/stabilized coronary segments than atorvastatin alone in the majority of patients (chi-square test 13.61, p < 0.005).
Conclusion:
Specific Lp(a) apheresis for 18 months produced coronary atherosclerosis regression in stable CHD patients with high Lp(a) levels and reached LDL-C goals.
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