Int J Angiol 2012; 21(01): 029-034
DOI: 10.1055/s-0032-1306418
Original Article
Thieme Medical Publishers 333 Seventh Avenue, New York, NY 10001, USA.

The Relationship of Serum Soluble Fas Ligand (sFasL) Level with the Extent of Coronary Artery Disease

Asife Sahinarslan
1   Department of Cardiology, School of Medicine, Gazi University, Ankara, Turkey
,
Bulent Boyaci
1   Department of Cardiology, School of Medicine, Gazi University, Ankara, Turkey
,
Sinan Altan Kocaman
1   Department of Cardiology, School of Medicine, Gazi University, Ankara, Turkey
,
Salih Topal
1   Department of Cardiology, School of Medicine, Gazi University, Ankara, Turkey
,
Ugur Ercin
2   Department of Biochemistry, School of Medicine, Gazi University, Ankara, Turkey
,
Kaan Okyay
1   Department of Cardiology, School of Medicine, Gazi University, Ankara, Turkey
,
Neslihan Bukan
2   Department of Biochemistry, School of Medicine, Gazi University, Ankara, Turkey
,
Ridvan Yalçin
1   Department of Cardiology, School of Medicine, Gazi University, Ankara, Turkey
,
Atiye Cengel
1   Department of Cardiology, School of Medicine, Gazi University, Ankara, Turkey
› Author Affiliations
Further Information

Publication History

Publication Date:
07 March 2012 (online)

Abstract

Fas/Fas ligand system contributes to the programmed cell death induced by myocardial ischemia. We investigated whether serum soluble Fas ligand (sFasL) level is independently related with the severity and extent of angiographically assessed coronary artery disease (CAD). We included 169 patients in this study. Two groups were formed based on the existence of a lesion on coronary angiography. First group included patients with normal coronary arteries (NCA; n = 53). Patients with atherosclerotic lesions were included in the second group (n = 116). We used the coronary vessel score (the number of the coronary arteries with a lesion leading to ≥ 50% luminal obstruction) and the Azar score to determine the extent and the severity of CAD. Standard enzyme-linked immunosorbent assay kits were used to measure serum sFasL levels. The serum sFasL level was higher in patients with CAD than in patients with NCA (0.52 ± 0.23 mU/mL vs. 0.45 ± 0.18 mU/mL, p = 0.023). The sFasL level correlated with Azar score (r = 0.231, p = 0.003) and with coronary vessel score (r = 0.269, p < 0.001). In the multivariate analysis, we found that age (beta: 0.188, p = 0.008), gender (beta: 0.317, p < 0.001), diabetes mellitus (DM; beta: 0.195, p = 0.008), and sFasL level (beta: 0.209, p = 0.003) were independently related with Azar score. When we used coronary vessel score as the dependent variable, we found that age (p = 0.020), gender (p < 0.001), DM (p = 0.006), and sFasL level (p = 0.001) were independent predictors. Serum sFasL level is associated with angiographically more severe CAD. Our findings suggest that sFasL level may be a biochemical surrogate of severe coronary atherosclerosis.

Note

This study was supported by the Scientific Investigation Projects Department of Gazi University.


 
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