Apolipoprotein M in patients with chronic kidney disease

Ida MH Sørensen, Marianne Bertelsen, Ellen Freese, Kristine Lindhard, Henrik Ullum, Bo Feldt-Rasmussen, Lars Bo Nielsen, Christina Christoffersen, Susanne Bro*

*Corresponding author for this work
8 Citations (Scopus)

Abstract

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.

Original languageEnglish
JournalAtherosclerosis
Volume275
Pages (from-to)304-311
ISSN0021-9150
DOIs
Publication statusPublished - 2018

Keywords

  • Cardiovascular risk
  • Chronic kidney disease
  • HDL cholesterol
  • LDL-cholesterol
  • Plasma apolipoprotein M
  • Urine apolipoprotein M sphingosine-1-phosphate

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