Why the study?
Does the presence, extent, and clinical stability of coronary artery disease affect endothelial function parameters, C-reactive protein, and homocysteine levels?
Does the presence, extent, and clinical stability of coronary artery disease affect endothelial function parameters, C-reactive protein, and homocysteine levels?
Vascular cell adhesion molecule-1 and sE-selectin are useful markers for the presence of coronary atherosclerosis, whereas C-reactive protein, troponin I, and leukocyte counts are predictors of clinical stability.
May support VCAM-1 and sE-selectin as CAD presence markers; hypothesis-generating, needs prospective validation before clinical use.
The aim of the study was to evaluate the effects of the presence, extent, and clinical stability of coronary artery disease on endothelial function parameters, C-reactive protein and homocysteine levels. Fifty-eight patients with angiographically documented coronary artery disease and 25 patients with normal coronary arteries were evaluated for risk factors, plasma homocysteine, C-reactive protein, and soluble adhesion molecule levels. Vascular cell adhesion molecule-1 and sE-selectin were significantly higher in the group with coronary artery disease than in healthy subjects (p = 0.005 and p = 0.031, respectively). Patients with unstable angina had significantly higher C-reactive protein (p < 0.001), troponin I (p < 0.01), and leukocyte counts (p < 0.05) than those with stable angina. sE-selectin levels were correlated with the extent of coronary atherosclerosis (r = 0.444, p < 0.05), and plasma homocysteine levels were associated with vascular cell adhesion molecule-1 (r = 0.479, p < 0.05) in unstable cases. These results suggest that vascular cell adhesion molecule-1 and sE-selectin are useful for determining the presence of coronary atherosclerosis, whereas C-reactive protein, troponin 1, and leukocyte count are predictors of clinical stability.
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Yı́ldı́rı́r et al. (2001) studied this question.
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