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Updated: Jul 5, 2026

Cholesterol Efflux Assay
Published on: March 6, 2012
Cholesteryl ester transfer protein activity and cardiovascular events in patients with chronic kidney disease stage V
Sarah Seiler1, Axel Schlitt, Xian-Cheng Jiang
1Department of Medicine IV, Saarland University, Homburg/Saar, Germany. Sarahseiler@gmx.de
Insights
In chronic kidney disease (CKD) patients, high cholesteryl ester transfer protein (CETP) activity and low HDL-cholesterol did not increase cardiovascular event risk. CETP inhibitors may not benefit these patients.
Area of Science:
- Nephrology
- Cardiology
- Lipidology
Background:
- Patients with chronic kidney disease (CKD) face a higher risk of cardiovascular events (CVE).
- Uraemic dyslipidaemia, characterized by low HDL-cholesterol (HDL-C) and high triglycerides, contributes to this risk.
- Cholesteryl ester transfer protein (CETP) reduces HDL-C by transferring cholesterol esters.
Purpose of the Study:
- To investigate the association between CETP activity and CVE in patients with CKD stage V.
- To determine if CETP activity correlates with HDL-C levels in this population.
Main Methods:
- Measured CETP activity and cholesterol levels in 69 haemodialysis patients.
- Prospectively assessed CVE and death over a 48-month follow-up period.
Main Results:
- CETP activity was negatively correlated with HDL-C in patients not on lipid-lowering medication (r = -0.379, P = 0.005).
- No significant difference in CETP activity was observed between patients with and without cardiovascular disease at baseline or for incident CVE during follow-up.
- Stratifying patients by median CETP activity or median HDL-C did not reveal an increased risk for CVE or death.
Conclusions:
- Despite a correlation between CETP activity and HDL-C, neither high CETP activity nor low HDL-C was linked to CVE in CKD stage V patients.
- Pharmacological modification of HDL-C using CETP inhibitors may have limited clinical value in this patient group.
Background:
Patients with chronic kidney disease (CKD) have an increased risk for cardiovascular events (CVE). Uraemic dyslipidaemia, which is characterized by low HDL-cholesterol (HDL-C) and elevated triglycerides' levels, may contribute to this elevated cardiovascular risk. Cholesteryl ester transfer protein (CETP) lowers HDL-C by transferring cholesterol esters to LDL and VLDL particles. We tested the hypothesis that CETP activity is associated with CVE in patients with CKD stage V.
Methods:
We measured CETP activity and cholesterol levels in 69 haemodialysis patients. CVE and death were prospectively assessed over a follow-up period of 48 months.
Results:
CETP activity was negatively correlated with HDL-C levels in patients without lipid-lowering medication (r = -0.379, P = 0.005). We found no difference in CETP activity in patients with cardiovascular disease at baseline compared to patients without cardiovascular disease. The same was true for incident CVE during the follow-up. When stratifying patients by median CETP activity, patients with high CETP activity did not have an increased risk for CVE (P = 0.901 by the log-rank test) or death (P = 0.615). Similarly, after stratifying patients by median HDL-C no increased risk for CVE (P = 0.780) or death (P = 0.838) was found in patients with low HDL-C.
Conclusions:
In summary, although CETP activity correlated with HDL-C levels, neither high CETP activity nor low HDL-C was associated with CVE in CKD stage V patients. Thus, pharmacological modification of HDL-C by CETP inhibitors seems to be of questionable value in these patients.
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