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Among inflammation and coagulation markers, PAI-1 is a true component of the metabolic syndrome

I Mertens1, A Verrijken, J J Michiels

  • 1Department of Diabetology, Metabolism and Clinical Nutrition, Faculty of Medicine, University Hospital Antwerp, University of Antwerp (UA), Antwerp, Belgium.

Insights

Metabolic syndrome is associated with increased leukocyte count and plasminogen activator inhibitor-1 activity (PAI-1). PAI-1 is a strong indicator, while leukocyte count is a moderate indicator of metabolic syndrome.

Area of Science:

  • Endocrinology
  • Cardiovascular Disease
  • Hematology

Background:

  • Metabolic syndrome is a cluster of conditions increasing cardiovascular disease risk.
  • Inflammatory markers and coagulation factors are implicated in metabolic syndrome pathogenesis.

Purpose of the Study:

  • To determine if leukocyte count, fibrinogen, von Willebrand factor (vWF), and plasminogen activator inhibitor-1 activity (PAI-1) are elevated in individuals with metabolic syndrome.
  • To assess these markers using both National Cholesterol Education Program-Adult Treatment Panel III (NCEP-ATPIII) and World Health Organization (WHO) criteria.

Main Methods:

  • A cross-sectional study of 520 overweight and obese subjects.
  • Metabolic syndrome assessed via NCEP-ATPIII and WHO criteria, including waist circumference, blood pressure, glucose, and lipids.
  • Leukocyte count, fibrinogen, vWF, and PAI-1 activity measured.

Main Results:

  • Subjects with metabolic syndrome showed significantly higher leukocyte count and PAI-1 activity by NCEP-ATPIII criteria.
  • Similar findings were observed with WHO criteria, with vWF also elevated.
  • Leukocyte count, vWF, and PAI-1 levels differed significantly based on the number of metabolic syndrome components present.

Conclusions:

  • Plasminogen activator inhibitor-1 activity (PAI-1) is strongly associated with metabolic syndrome.
  • Leukocyte count shows a moderate association, while vWF and fibrinogen have a weaker association with metabolic syndrome.
Abstract

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