Abstract

Objective: Increased levels of fibrinogen and plasminogen activator inhibitor 1 (PAI-1) are associated with an increased risk of ischemic coronary disease and its complications. Since atherogenic dyslipidemias are well-known risk factors for coronary heart disease, this study aimed to determine whether Type IIb dyslipidemia, one of the most atherogenic dyslipidemias, is accompanied by increased PAI-1 and fibrinogen synthesis. The additional aim of this study was to evaluate the effect of micronized fibrates on the levels of PAI-1 and fibrinogen in patients with Type IIb dyslipidemia. Subjects: Thirty patients with Type IIb dyslipidemia and 12 age-matched control subjects were studied. Fourteen patients were treated with fenofibrate and 16 were treated with ciprofibrate for 1 month. Methods: Plasma PAI-1 levels were measured by the ELISA method with Diagnostica Stago kit. The level of fibrinogen was measured by the Clauss method. Results: PAI-1 levels in dyslipidemic patients before treatment differed significantly in both the fenofibrate and ciprofibrate treatment groups (101.18 ± 36.47 ng/ml, 87.64 ± 32.06 ng/ml, respectively) from those in the control group (32.32 ± 7.39 ng/ml, p < 0.001). Compared with the control subjects (2.91 ± 0.35 g/l), fibrinogen levels before treatment were higher in patients with dyslipidemia treated with ciprofibrate (3.42 ± 0.59 g/l, NS) and fenofibrate (3.65 ± 1.10 g/l, p < 0.05). One-month ciprofibrate treatment resulted in an insignificant decrease in PAI-1 levels (76.28 ± 21.60 ng/ml, NS) and in a significant decrease in fibrinogen levels (2.73 ± 0.40 g/l, p < 0.01). After one-month fenofibrate treatment PAI-1 levels (81.22 ± 25.01 ng/ml, p < 0.01) and fibrinogen levels (2.95 ± 0.72 g/l, p < 0.01) decreased significantly. Conclusion: Type IIb dyslipidemic patients have increased levels of PAI-1 and fibrinogen. Micronized fibrates decreased not only lipid levels but also the levels of fibrinogen and PAI-1 in these patients.

Author Details

Authors

• B. Okopien¹
• L. Cwalina¹
• M. Lebek¹
• J. Kowalski¹
• M. Zielinski¹
• M. Wisniewska-Wanat²
• Z. Kalina²
• Z.S. Herman¹

Departments

• ¹ Department of Clinical Pharmacology, and
• ² Department of Internal Diseases and Clinical Pharmacology, Medical University of Silesia, Katowice, Poland

Address

Dr. B. Okopien; Department of Clinical Pharmacology, Medical University of Silesia, Medyków 18, 40-752 Katowice, Poland

Citation