Apolipoprotein M in patients with chronic kidney disease
Related Experiment Video
Updated: Feb 8, 2026

Assessment of Vascular Function in Patients With Chronic Kidney Disease
Published on: June 16, 2014
Ida Mh Sørensen1, Marianne Bertelsen1, Ellen Freese1
1Department of Nephrology, Rigshospitalet, Copenhagen, Denmark.
Background And Aims:
Plasma apolipoprotein M (APOM) is bound to HDL-particles and has anti-atherogenic effects. The present study explored whether plasma APOM is reduced in patients with chronic kidney disease (CKD), and associated with cardiovascular disease (CVD). In addition, we tested the hypothesis that the excretion of APOM into the urine is increased in patients with kidney disease.
Methods:
Plasma samples were collected from a cohort of patients with CKD stages 1 to 5D (N = 409) and controls (N = 35). Urine was collected from 47 subjects. Plasma APOM was measured with sandwich ELISA and urine APOM with competitive ELISA.
Results:
Plasma APOM levels were reduced in patients with CKD stages 3-5D as compared to patients with CKD stages 1 + 2 and controls (p < 0.01). CKD patients with known CVD displayed even further reduction in plasma APOM levels than CKD patients without known CVD (p < 0.001). Fast-phase liquid chromatography showed that plasma APOM was primarily associated with HDL-cholesterol (HDL-C) across CKD stages. Accordingly, when plasma APOM values were corrected for HDL-C, a significant difference only persisted between patients with CKD stage 3 and stages 1 + 2 (p < 0.05), and the difference between CKD patients with and without known CVD disappeared. Urine APOM/creatinine ratio was not significantly increased in patients with kidney disease.
Conclusions:
The results show that the difference in plasma APOM levels observed between patients with mild and advanced CKD may mainly be due to differences in plasma HDL-C. Whether APOM plays a role in human uremic atherogenesis warrants further experimental studies.
Insights
Plasma apolipoprotein M (APOM) is reduced in advanced chronic kidney disease (CKD) and associated with cardiovascular disease (CVD). This reduction is largely explained by changes in HDL-cholesterol, not increased urinary excretion.
Area of Science:
- Cardiovascular Research
- Nephrology
- Biochemistry
Background:
- Plasma apolipoprotein M (APOM) exhibits anti-atherogenic properties.
- Its role in chronic kidney disease (CKD) and cardiovascular disease (CVD) is not fully understood.
- APOM is known to be associated with HDL-particles.
Purpose of the Study:
- To investigate plasma APOM levels in patients with varying stages of CKD.
- To determine the association between plasma APOM and cardiovascular disease (CVD) in CKD patients.
- To examine urinary APOM excretion in kidney disease.
Main Methods:
- Plasma and urine samples from 409 CKD patients (stages 1-5D) and 35 controls were analyzed.
- Plasma APOM was quantified using sandwich ELISA; urine APOM was measured by competitive ELISA.
- Association with HDL-cholesterol was assessed using fast-phase liquid chromatography.
Main Results:
- Plasma APOM was significantly reduced in CKD stages 3-5D compared to earlier stages and controls.
- CKD patients with CVD showed lower plasma APOM than those without CVD.
- After adjusting for HDL-cholesterol, the differences in plasma APOM between CKD stages and CVD status diminished. Urinary APOM excretion was not elevated.
Conclusions:
- Observed differences in plasma APOM in CKD are primarily linked to alterations in HDL-cholesterol levels.
- The specific role of APOM in uremic atherogenesis requires further investigation.
- Urinary APOM excretion does not appear to increase in kidney disease.
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