Literature DB >> 23450131

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

Asife Sahinarslan1, Bulent Boyaci, Sinan Altan Kocaman, Salih Topal, Ugur Ercin, Kaan Okyay, Neslihan Bukan, Ridvan Yalçin, Atiye Cengel.   

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.

Entities:  

Keywords:  apoptosis; atherosclerosis; ischemic heart disease; soluble fas ligand

Year:  2012        PMID: 23450131      PMCID: PMC3444027          DOI: 10.1055/s-0032-1306418

Source DB:  PubMed          Journal:  Int J Angiol        ISSN: 1061-1711


  26 in total

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Journal:  J Am Coll Cardiol       Date:  2002-02-20       Impact factor: 24.094

2.  Soluble Fas is a marker of coronary artery disease in patients with end-stage renal disease.

Authors:  M J Hébert; M Masse; N Vigneault; I Sirois; S Troyanov; F Madore
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3.  Serum matrix metalloproteinase-9 concentration in angiographically assessed coronary artery disease.

Authors:  A Kalela; T A Koivu; T Sisto; J Kanervisto; M Höyhtyä; P Sillanaukee; T Lehtimäki; S T Nikkari
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4.  Soluble Fas ligand and atherosclerosis in hypertensive patients.

Authors:  Takafumi Okura; Sanae Watanabe; Yinong Jiang; Michitsugu Nakamura; Yasunori Takata; Zhao-Hui Yang; Katsuhiko Kohara; Yutaka Kitami; Kunio Hiwada
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5.  Ongoing myocardial damage in chronic heart failure is related to activated tumor necrosis factor and Fas/Fas ligand system.

Authors:  Koichi Setsuta; Yoshihiko Seino; Takeshi Ogawa; Toshiaki Ohtsuka; Kohji Seimiya; Teruo Takano
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6.  Decreased circulating Fas ligand in patients with familial combined hyperlipidemia or carotid atherosclerosis: normalization by atorvastatin.

Authors:  Luis Miguel Blanco-Colio; Jose Luis Martín-Ventura; Josep M Sol; Cristina Díaz; Gonzalo Hernández; Jesús Egido
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Review 7.  The Fas death factor.

Authors:  S Nagata; P Golstein
Journal:  Science       Date:  1995-03-10       Impact factor: 47.728

8.  Arterial smooth muscle cells express nitric oxide synthase in response to endothelial injury.

Authors:  G K Hansson; Y J Geng; J Holm; P Hårdhammar; A Wennmalm; E Jennische
Journal:  J Exp Med       Date:  1994-08-01       Impact factor: 14.307

9.  Metalloproteinase-mediated release of human Fas ligand.

Authors:  N Kayagaki; A Kawasaki; T Ebata; H Ohmoto; S Ikeda; S Inoue; K Yoshino; K Okumura; H Yagita
Journal:  J Exp Med       Date:  1995-12-01       Impact factor: 14.307

10.  Fas and Fas ligand in embryos and adult mice: ligand expression in several immune-privileged tissues and coexpression in adult tissues characterized by apoptotic cell turnover.

Authors:  L E French; M Hahne; I Viard; G Radlgruber; R Zanone; K Becker; C Müller; J Tschopp
Journal:  J Cell Biol       Date:  1996-04       Impact factor: 10.539

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Journal:  Int J Clin Exp Pathol       Date:  2015-11-01

2.  Lymphocyte Apoptosis and FAS Expression in Patients with 22q11.2 Deletion Syndrome.

Authors:  Dina M Aresvik; Torstein Øverland; Kari Lima; Rolf D Pettersen; Tore G Abrahamsen
Journal:  J Clin Immunol       Date:  2018-12-19       Impact factor: 8.317

3.  Novel association of the obesity risk-allele near Fas Apoptotic Inhibitory Molecule 2 (FAIM2) gene with heart rate and study of its effects on myocardial infarction in diabetic participants of the PREDIMED trial.

Authors:  Dolores Corella; Jose V Sorlí; José I González; Carolina Ortega; Montserrat Fitó; Monica Bulló; Miguel Angel Martínez-González; Emilio Ros; Fernando Arós; José Lapetra; Enrique Gómez-Gracia; Lluís Serra-Majem; Valentina Ruiz-Gutierrez; Miquel Fiol; Oscar Coltell; Ernest Vinyoles; Xavier Pintó; Amelia Martí; Carmen Saiz; José M Ordovás; Ramón Estruch
Journal:  Cardiovasc Diabetol       Date:  2014-01-06       Impact factor: 9.951

4.  Baseline Ratio of Soluble Fas/FasL Predicts Onset of Pulmonary Hypertension in Elder Patients Undergoing Maintenance Hemodialysis: A Prospective Cohort Study.

Authors:  Xiao-Han Ding; Xiaoliang Chai; Jin Zheng; Hong Chang; Wenxue Zheng; Shi-Zhu Bian; Ping Ye
Journal:  Front Physiol       Date:  2022-03-01       Impact factor: 4.566

  4 in total

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