Inflammatory Markers in Men with Angiographically Documented Coronary Heart Disease

Author:

Rifai Nader1,Joubran Rana2,Yu Harry1,Asmi Mohamad3,Jouma Mohidien2

Affiliation:

1. Department of Laboratory Medicine, Children’s Hospital, and Department of Pathology, Harvard Medical School, Boston, MA 02115

2. Department of Biochemistry, School of Pharmacy, University of Damascus, Damascus, Syria

3. Department of Cardiology, University of Damascus Hospitals, Damascus, Syria

Abstract

Abstract Background: Recent evidence suggests that atherosclerosis is a chronic inflammatory process. In this study, we examined several markers of inflammation in men with coronary heart disease (CHD) and appropriate controls. Methods: The concentrations of C-reactive protein (CRP), serum amyloid A (SAA), interleukin-6 (IL-6), and soluble intracellular adhesion molecule (sICAM-1) were examined in 100 men with angiographically documented CHD and 100 age-, gender-, and smoking-matched controls with no history of CHD. We assessed the association of these markers with severity of disease as indicated by >50% obstruction in one vessel (n = 30), two vessels (n = 39), or three vessels (n = 31). Results: Significant increases were noted in serum CRP (median for cases vs controls, 3.4 vs 1.5 mg/L; P <0.0001), SAA (5.9 vs 3.7 mg/L; P <0.005), and IL-6 (2.3 vs 1.7 ng/L; P <0.013) in patients with CHD compared with controls. These differences remained significant after correction for age, smoking, hypertension, diabetes, and lipid and homocysteine concentrations. Plasma sICAM-1 was not significantly different between the two groups (335 vs 339 μg/L). No significant correlation was seen between these markers and the severity of coronary disease. Conclusions: Concentrations of CRP, SAA, and IL-6 were increased in patients with CHD but failed to correlate with severity of coronary disease. These markers might reflect the diffuse atherosclerotic process in the vascular system rather than the degree of localized obstruction from coronary lesions.

Publisher

Oxford University Press (OUP)

Subject

Biochemistry, medical,Clinical Biochemistry

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