Total and high molecular weight adiponectin in patients with coronary artery disease

Ayman El-Menyar1, Nasser Rizk, Abdulrahman D Al Nabti

  • 1Department of Cardiology and Cardiovascular Surgery, Qatar.

Insights

High molecular weight adiponectin (HMW) may be a superior biomarker for coronary artery disease (CAD) compared to total adiponectin. Lower HMW adiponectin levels in diabetics may explain their poorer CAD outcomes.

Area of Science:

  • Cardiovascular Research
  • Metabolic Syndrome Studies
  • Biomarker Discovery

Background:

  • Serum adiponectin levels are inversely associated with coronary artery disease (CAD) severity.
  • Understanding specific adiponectin isoforms, like high molecular weight adiponectin (HMW), is crucial for refining cardiovascular risk assessment.

Purpose of the Study:

  • To evaluate the clinical significance of measuring both total and HMW adiponectin.
  • To compare adiponectin levels in peripheral veins versus coronary artery ostia in CAD patients.

Main Methods:

  • Simultaneous measurement of total and HMW adiponectin in coronary ostia and peripheral veins.
  • Inclusion of 134 patients: 57 with acute coronary syndrome (ACS), 44 with stable angina, and 33 healthy controls.
  • Analysis of venous lipid profiles, inflammatory markers (CRP, TNF-α, IL-6), and insulin levels.

Main Results:

  • HMW adiponectin in coronary ostia correlated with venous total and HMW adiponectin levels.
  • CAD patients exhibited lower mean total and HMW adiponectin levels compared to controls.
  • Ostial HMW adiponectin was higher in ACS patients than stable angina patients.
  • Diabetic CAD patients had significantly lower ostial total and HMW adiponectin levels than non-diabetic CAD patients.

Conclusions:

  • HMW adiponectin and its ratio to total adiponectin may serve as improved biomarkers for CAD.
  • Ostial adiponectin levels in ACS could reflect redistribution to acute lesions.
  • Diminished HMW adiponectin in diabetes mellitus may contribute to worse CAD outcomes in this population.
Abstract

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