Cardiovascular mortality and microinflammation in abdominal obese hemodialysis patients

Srčnožilna umrljivost in mikrovnetje pri trebušno debelih hemodializnih bolnikih

Authors

  • Sebastjan Bevc University of Maribor, Faculty of Medicine ; University Medical Centre Maribor, Clinic of Internal Medicine, Department of Nephrology Author
  • Tadej Zorman University Medical Centre Maribor, Clinic of Internal Medicine, Department of Nephrology Author
  • Darinka Purg University Medical Centre Maribor, Clinic of Internal Medicine, Department of Nephrology Author
  • Robert Ekart University Medical Centre Maribor, Clinic of Internal Medicine, Department of Dialysis ; University of Maribor, Faculty of Medicine Author
  • Radovan Hojs University Medical Centre Maribor, Clinic of Internal Medicine, Department of Nephrology ; University of Maribor, Faculty of Medicine Author

DOI:

https://doi.org/10.18690/actabiomed.90

Keywords:

microinflammation, inflammatory mediators, cardiovascular mortality, abdominal obesity, hemodialysis

Abstract

Purpose: Abdominal adipose tissue has important inflammatory properties and is a source of various inflammatory mediators. Given that concentrations of some inflammatory mediators are high among hemodialysis (HD) patients, abdominal obesity may play an important role in the pathogenesis of microinflammation which is known to be associated with accelerated atherosclerosis. The aim of our study was to determine the impact of microinflammation on cardiovascular (CV) mortality in abdominal obese HD patients.

Methods: Seventy–one HD patients (mean age 59.3 ± 12.8 years) were included in our study. Waist circumference (WAC) was measured and abdominal obesity was defined according to the International Diabetes Federation. Serum levels of lipids (triglycerides, high density lipoproteins (HDL) cholesterol, low density lipoproteins (LDL) cholesterol) and inflammatory mediators (interleukin–6, tumor necrosis factor–alpha, vascular cellular adhesion molecule–1 (VCAM–1), intercellular adhesion molecule–1 (ICAM–1)) were measured. Patients were observed from the date of measurement (November 2003) of inflammatory mediators until their death or to 10th of November 2009.

Results: The mean WAC value for men was 97.6 ± 16.1 cm, and for women 92.2 ± 15.9 cm. Abdominal obesity was found in 62% of the enrolled patients. Cox regression analysis showed that the inflammatory mediators VCAM–1 (p<0.031) and ICAM–1 (p<0.024) were predictors of CV mortality in abdominal obese HD patients. Both inflammatory mediators remained predictors of CV mortality if age and other known risk factors for atherosclerosis (arterial hypertension, smoking, HDL and LDL cholesterol and triglycerides) were included in the analysis.

Conclusion: The results of our study indicate that microinflammation is associated with CV mortality in abdominal obese HD patients.

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Author Biographies

  • Sebastjan Bevc, University of Maribor, Faculty of Medicine ; University Medical Centre Maribor, Clinic of Internal Medicine, Department of Nephrology

    Assist. Prof., M.D., Maribor, Slovenia. E–mail: sebastjan.bevc@gmail.com, sebastjan.bevc@ukc–mb.si

  • Tadej Zorman, University Medical Centre Maribor, Clinic of Internal Medicine, Department of Nephrology

    Maribor, Slovenia.

  • Darinka Purg, University Medical Centre Maribor, Clinic of Internal Medicine, Department of Nephrology

    Maribor, Slovenia.

  • Robert Ekart, University Medical Centre Maribor, Clinic of Internal Medicine, Department of Dialysis ; University of Maribor, Faculty of Medicine

    Maribor, Slovenia.

  • Radovan Hojs, University Medical Centre Maribor, Clinic of Internal Medicine, Department of Nephrology ; University of Maribor, Faculty of Medicine

    Maribor, Slovenia.

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Published

28.11.2021

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Section

Articles

How to Cite

Cardiovascular mortality and microinflammation in abdominal obese hemodialysis patients: Srčnožilna umrljivost in mikrovnetje pri trebušno debelih hemodializnih bolnikih . (2021). Acta Medico-Biotechnica, 6(2), 39-46. https://doi.org/10.18690/actabiomed.90