The Association between the Epicardial Adipose Tissue Thickness and Oxidative Stress Parameters in Isolated Metabolic Syndrome Patients: A Multimarker Approach

Author:

Demir Bulent1,Demir Esra2,Acıksarı Gonul3,Uygun Turgut1,Utku Irem Kırac2,Gedikbasi Asuman4,Caglar Ilker Murat1,Pirhan Osman1,Tureli Hande Oktay1,Oflar Ersan1,Ungan İsmail1,Ciftci Serkan1,Karakaya Osman1

Affiliation:

1. Department of Cardiology, Bakırkoy Dr. Sadi Konuk Education and Research Hospital, Tevfik Sağlam Caddesi No. 11, Zuhuratbaba Mahallesi, Bakırköy, 34156 Istanbul, Turkey

2. Department of İnternal Medicine, Bakırkoy Dr. Sadi Konuk Education and Research Hospital, Turkey

3. Department of Cardiology, İstinye State Hospital, Turkey

4. Department of Biochemistry, Bakırkoy Dr. Sadi Konuk Education and Research Hospital, Turkey

Abstract

The risk for cardiovascular diseases and type 2 diabetes mellitus significantly increases in the patient population with metabolic syndrome (MeS). The present study aimed to investigate the association between the epicardial adipose tissue thickness (EATT) and the oxidative stress parameters in MeS patients. The study included 181 patients as a patient group of 92 consecutive patients with MeS and a control group of 89 consecutive patients with similar age and gender. EATT was evaluated by transthoracic echocardiography. Serum levels of total oxidant status (TOS), total antioxidative capacity (TAS), paraoxonase-1 (PON-1), and arylesterase activities were measured. EATT was higher in the MeS group compared to the control group (6.0 ± 2.0 mm and4.0 ± 1.0 mm, resp.;P<0.001). The level of TOS was higher in the MeS group compared to the control group (P<0.001). Additionally, the TAS level was higher in the MeS group compared to the control group (P<0.001). Furthermore, the serum levels of PON-1 and arylesterase were lower in the MeS group compared to the control group (P<0.001). EAT may cause an increased risk of cardiovascular diseases by leading to increased oxidative stress in patients with MeS.

Publisher

Hindawi Limited

Subject

Endocrine and Autonomic Systems,Endocrinology,Endocrinology, Diabetes and Metabolism

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