Related Experiment Video
Updated: Jun 16, 2026

High-Density Lipoprotein-Specific Phospholipid Efflux Assay
Published on: September 30, 2025
Extracorporeal LDL cholesterol elimination (25 years of experience in CZ)
12nd Department of Internal Medicine, Charles University School of Medicine and Teaching Hospital, Hradec Králové, CZ. blaham@email.cz
Insights
Long-term LDL-apheresis and hemorheopheresis effectively reduce LDL-cholesterol in severe familial hypercholesterolemia (FH) patients. These therapies demonstrate good tolerance and minimal complications, with potential benefits for microcirculation.
Area of Science:
- Cardiology
- Nephrology
- Vascular Biology
Background:
- Severe familial hypercholesterolemia (FH) requires advanced treatment strategies.
- Extracorporeal elimination therapies like LDL-apheresis and hemorheopheresis are centralized in the Czech Republic for FH management.
Purpose of the Study:
- To evaluate the long-term efficacy and safety of LDL-apheresis and hemorheopheresis in patients with severe FH.
- To assess the impact of these therapies on cardiovascular risk markers and microcirculation.
Main Methods:
- Long-term follow-up (3-12 years) of 12 FH patients (3 homozygous, 9 heterozygous).
- Treatment modalities included LDL-apheresis (n=9) and hemorheopheresis (n=3).
- Assessment of lipid profiles, ApoB, Lp(a), carotid intima-media thickness, and selected biomarkers.
Main Results:
- LDL-apheresis and hemorheopheresis significantly reduced LDL-cholesterol (by ~82%), ApoB (by ~73%), and Lp(a) (by ~82%).
- Carotid intima-media thickness improved or stabilized in 75% of patients.
- Therapies showed good tolerance with only 5.6% clinically irrelevant side-effects.
Conclusions:
- LDL-apheresis and hemorheopheresis are effective and well-tolerated long-term treatments for severe FH.
- While specific biomarkers for disease activity remain elusive, these procedures offer substantial lipid reduction and potential microcirculatory benefits.
Abstract:
In the Czech Republic the therapy of severe familial hypercholesterolemia (FH) by extracorporeal elimination using LDL-apheresis (immunoadsorption) and hemorheopheresis is concentrated into one center. The authors evaluate the long-term therapy (3-12 years, median 7,25) in 12 patients with FH - 3 homozygous, 9 heterozygous; Fredrickson type IIa, IIb (treated: 9 by LDL-apheresis and 3 by hemorheopheresis). Immunoapheretic interventions decrease LDL-cholesterol, ApoB and even Lp(a) by about 82 +/- 1; 73 +/- 13; 82 +/- 19 %, respectively. Selected non-invasive methods are important for a long-term and repeated follow-up. Carotid intima-media thickness showed improvement or stagnation in 75% of the patients. The level of some adhesive molecules, cytokines, endoglin and some coagulation functions were measured, but no universally accepted biomarkers informing of the actual activity of the disease were found to predict and plan the therapy. A program for procedure planning with the use of Microsoft® Excel for Windows® was developed. In summary, LDL-apheresis and hemorheopheresis substantially lower LDL-cholesterol in FH. Our experience with long-term therapy also shows good tolerance and a small number of complications (5,6% of clinically irrelevant side-effects). Hemorheopheresis may improve blood flow in microcirculation in familial hypercholesterolemia and also in some other disorders of microcirculation.
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