Elevated plasma migration inhibitory factor in hypertension-hyperlipidemia patients correlates with impaired endothelial function

Medicine (Baltimore). 2016 Oct;95(43):e5207. doi: 10.1097/MD.0000000000005207.

Abstract

Migration inhibitory factor (MIF) has been shown to be critical in the pathology of early artherosclerosis; this article aim to investigate the plasma levels of MIF in hypertension plus hyperlipidemia patients.A total of 39 hypertension plus hyperlipidemia patients without any previous treatment were enrolled (HTN-HLP). Twenty-five healthy subjects were enrolled as the healthy control group (HEALTHY). Plasma MIF was measured by ELISA; laboratory and clinical characteristics were analyzed. HUVECs were treated with pooled plasma from HTN-HLP and HEALTHY groups, and the protein levels of adhesion molecules VCAM-1 and ICAM-1 were determined by ELISA. We found that plasma MIF was significantly elevated in the HTN-HLP group. Serum NO and eNOS levels were significantly lower; serum ET-1 (endothelin) levels were significantly higher in the HTN-HLP group. Furthermore, blood pressure, baPWV (brachial-ankle pulse wave velocity), and serum ET-1 level were significantly positively; serum NO and eNOS levels were negatively correlated with plasma MIF levels. Plasma from HTN-HLP significantly stimulated VCAM-1 and ICAM-1 protein expression on the surface of HUVECs.Plasma MIF was elevated in HTN-HLP patients and correlates with impaired endothelial function.

Publication types

  • Observational Study

MeSH terms

  • Adult
  • Ankle Brachial Index
  • Blood Pressure / physiology*
  • Cells, Cultured
  • Endothelium, Vascular / physiopathology*
  • Female
  • Follow-Up Studies
  • Humans
  • Hyperlipidemias / blood*
  • Hyperlipidemias / complications
  • Hypertension / blood*
  • Hypertension / complications
  • Hypertension / physiopathology
  • Macrophage Migration-Inhibitory Factors / blood*
  • Male
  • Middle Aged
  • Retrospective Studies
  • Umbilical Veins / pathology
  • Umbilical Veins / physiopathology

Substances

  • Macrophage Migration-Inhibitory Factors