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Circulating soluble lectin-like oxidized low-density lipoprotein receptor-1 levels are associated with proximal/middle segment of the LAD lesions in patients with stable coronary artery disease.

AbstractBACKGROUND/OBJECTIVES:
Atherosclerosis is the main underlying pathology of coronary artery disease (CAD), which is the leading cause of mortality worldwide. Lectin-like oxidized low-density lipoprotein receptor-1 (LOX-1) is involved in multiple phases of vascular dysfunction, including endothelial dysfunction, atherosclerotic plaque formation, and destabilization. The purpose of the current study was to determine whether soluble LOX-1 is associated with proximal/mid and distal segment of the left anterior descending (LAD) artery lesion in patients with stable CAD.
METHODS:
Sixty-four patients with proximal/mid segment of the LAD lesions and 51 patients with distal segments of the LAD lesions were included in this study. Soluble LOX-1 levels were measured in all study subjects.
RESULTS:
Baseline characteristics of the two groups were similar. In stable CAD, patients with proximal/middle segment of the LAD lesions had significantly higher circulating soluble LOX-1 levels than patients with distal segments of the LAD lesions (1.07 ± 0.33 vs. 0.70 ± 0.17 ng/ml, p < 0.001). No correlation was found between plasma-soluble LOX-1 levels and fasting glucose, lipid profile. For predicting proximal/middle LAD lesions, the highest specificity (95,2%) and sensitivity (53,8%) levels were obtained at the cut-off value of 0.68.
CONCLUSION:
Our study demonstrated that serum-soluble LOX-1 levels were associated with proximal/mid segment of the LAD lesions. Furthermore, this study suggested soluble LOX-1 might be a useful biomarker of coronary plaque vulnerability in patients with stable CAD. Soluble LOX-1, the novel biochemical marker, may provide new insights into not only risk stratification but also therapeutic strategy for CAD.
AuthorsMehmet Balın, Ahmet Celik, M Ali Kobat
JournalClinical research in cardiology : official journal of the German Cardiac Society (Clin Res Cardiol) Vol. 101 Issue 4 Pg. 247-53 (Apr 2012) ISSN: 1861-0692 [Electronic] Germany
PMID22116101 (Publication Type: Journal Article)
Chemical References
  • Biomarkers
  • Lipids
  • OLR1 protein, human
  • Scavenger Receptors, Class E
  • Glucose
Topics
  • Aged
  • Biomarkers (metabolism)
  • Coronary Artery Disease (physiopathology)
  • Female
  • Glucose (metabolism)
  • Humans
  • Lipids (blood)
  • Male
  • Middle Aged
  • Plaque, Atherosclerotic (pathology)
  • Prospective Studies
  • Scavenger Receptors, Class E (metabolism)
  • Sensitivity and Specificity

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