Can vasohibin-1, an endothelium-derived angiogenesis inhibitor, be a marker of endothelial dysfunction in hemodialysis patients?


ALTUNÖREN O., Kerkutluoglu M., Sarisik F. N. , Akkus G., SEYİTHANOĞLU M., Doganer A., ...More

SEMINARS IN DIALYSIS, 2020 (Journal Indexed in SCI) identifier identifier identifier

  • Publication Type: Article / Article
  • Volume:
  • Publication Date: 2020
  • Doi Number: 10.1111/sdi.12899
  • Title of Journal : SEMINARS IN DIALYSIS

Abstract

Background Endothelial dysfunction (ED) is associated with high cardiovascular disease burden in hemodialysis (HD) patients. Vasohibin-1, an endothelium-derived angiogenesis inhibitor, is essential for endothelial cell survival, therefore it may be a promising marker of ED. We aimed to investigate whether vasohibin-1 levels are associated with ED markers in HD patients. Methods Fifty HD patients and 30 healthy controls were included in the study. As markers of ED, endothelium-dependent flow-mediated dilatation (FMD), carotid intima-media thickness (CIMT), and pulse wave velocity (PWV) were examined. Serum vasohibin-1 levels were measured with ELISA. Results Serum vasohibin-1 levels were low (387.7 +/- 115.7 vs 450.1 +/- 140.1P = .02), FMDs' were impaired (6.65 +/- 2.50 vs 10.95 +/- 2.86P < .001), PWV (7.92 +/- 1.964 vs 6.79 +/- 0.96P = .01) and CIMT (0.95 +/- 0.20 vs 0.60 +/- 0.11P < .001) were increased in HD patients compared to healthy controls. In regression analysis, vasohibin-1 levels were not related with FMD, PWV, or CIMT. Conclusions Hemodialysis patients have low serum vasohibin-1 levels but serum levels of vasohibin-1 did not show any significant relationship with FMD, PWV, and CIMT in HD patients. Since vasohibin-1 acts via paracrine pathways, serum levels may be insufficient to explain the relationship between vasohibin and ED. Local vasohibin-1 activity on tissue level may be more important instead of circulating levels.