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Updated: Dec 13, 2025

Cholesterol Efflux Assay
Published on: March 6, 2012
Low Plasma Lecithin: Cholesterol Acyltransferase (LCAT) Concentration Predicts Chronic Kidney Disease
Andrea Baragetti1, Alice Ossoli2, Arianna Strazzella2
1Dipartimento di Scienze Farmacologiche e Biomolecolari, Università degli Studi di Milano, 20133 Milano, Italy.
Insights
Low lecithin:cholesterol acyltransferase (LCAT) levels are linked to worsening kidney function in chronic kidney disease (CKD) patients and the general population, indicating LCAT
Area of Science:
- Nephrology
- Lipidology
- Biochemistry
Background:
- Low high-density lipoprotein-cholesterol (HDL-c) is a key lipid abnormality in chronic kidney disease (CKD).
- Reduced lecithin:cholesterol acyltransferase (LCAT) concentration is a primary driver of the low HDL-c phenotype in CKD patients.
Purpose of the Study:
- To investigate the hypothesis that diminished LCAT concentration in CKD contributes to the progression of renal damage.
- To assess the predictive value of LCAT levels for kidney function decline in both CKD patients and the general population.
Main Methods:
- Analysis of two cohorts from the PLIC study: 164 CKD patients (NefroPLIC) and 164 subjects with normal kidney function (PLIC).
- Categorization of patients based on LCAT concentration tertiles.
- Assessment of renal damage progression, kidney function impairment, and reactive oxygen species (ROS) production in renal cells.
Main Results:
- In CKD patients, the lowest LCAT tertile showed a significantly higher event rate compared to the highest tertile.
- In the general population cohort, the lowest LCAT tertile exhibited a faster decline in kidney function than the highest tertile.
- Serum from individuals with low LCAT levels promoted higher ROS production in renal cells, an effect mitigated by recombinant LCAT.
Conclusions:
- Reduced plasma LCAT concentration is a predictor of CKD progression in patients with renal dysfunction.
- Lower LCAT levels also predict kidney function impairment in the general population, highlighting LCAT's role in renal health.
Abstract:
Low high-density lipoprotein-cholesterol (HDL-c) is the most remarkable lipid trait both in mild-to-moderate chronic kidney disease (CKD) patients as well as in advanced renal disease stages, and we have previously shown that reduced lecithin:cholesterol acyltransferase (LCAT) concentration is a major determinant of the low HDL phenotype. In the present study, we test the hypothesis that reduced LCAT concentration in CKD contributes to the progression of renal damage. The study includes two cohorts of subjects selected from the PLIC study: a cohort of 164 patients with CKD (NefroPLIC cohort) and a cohort of 164 subjects selected from the PLIC participants with a basal estimated glomerular filtration rate (eGFR) > 60 mL/min/1.73 m2 (PLIC cohort). When the NefroPLIC patients were categorized according to the LCAT concentration, patients in the 1st tertile showed the highest event rate at follow-up with an event hazard ratio significantly higher compared to the 3rd LCAT tertile. Moreover, in the PLIC cohort, subjects in the 1st LCAT tertile showed a significantly faster impairment of kidney function compared to subjects in the 3rd LCAT tertile. Serum from subjects in the 1st LCAT tertile promoted a higher reactive oxygen species (ROS) production in renal cells compared to serum from subjects in the third LCAT tertile, and this effect was contrasted by pre-incubation with recombinant human LCAT (rhLCAT). The present study shows that reduced plasma LCAT concentration predicts CKD progression over time in patients with renal dysfunction, and, even more striking, it predicts the impairment of kidney function in the general population.
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