Abstract

Systemic lupus erythematosus (SLE) is characterized by chronic inflammation. Plasma atherogenic index (PAI) is a valuable marker for the cardiovascular disease and cardiac risk. The aim of this study was to evaluate the role and clinical use of PAI in atherosclerosis and the cardiac risk in SLE patients. We included 56 female SLE patients who were selected according to the American College of Rheumatology (1997) diagnosis criteria. Furthermore, we selected age-and body mass index (BMI)-matched 56 female healthy individuals. PAI was measured as a logarithmic value of triglyceride to high-density cholesterol ratio. We used carotid intima media thickness (cIMT) as an inflammatory marker because of its widespread use. The lipid and other biochemical parameters of patient and control groups were examined. The PAI and cIMT values of SLE patients were 0.04±0.23 and 0.78±0.18 mm, respectively. Besides, for the control group, the PAI value was -0.09±0.20 and cIMT value was 0.50±0.15 mm (p=0.002, p<0.001; respectively). There was a strong correlation between cIMT and PAI (r=0.273, p=0.003). According to the multiple logistic regression analysis, we found that PAI value is an independent factor for cIMT in SLE patients (odds ratio: 2.6, 95 % confidence interval; 1.506-4.374; p=0.029). We determined that PAI can be used as an independent indicator for subclinical atherosclerosis in SLE patients.

Highlights

  • Systemic lupus erythematosus (SLE) is a chronic inflammatory and autoimmune connective tissue disease characterized by multiple organ and system involvement

  • There was a strong correlation between carotid intima media thickness (cIMT) and Plasma atherogenic index (PAI) (r=0.273, p=0.003)

  • According to the multiple logistic regression analysis, we found that PAI value is an independent factor for cIMT in SLE patients

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Summary

Introduction

Systemic lupus erythematosus (SLE) is a chronic inflammatory and autoimmune connective tissue disease characterized by multiple organ and system involvement. The etiology has not yet been clarified [1]. Skin lesions, joint, renal, hematologic, and central nervous system involvements can be observed during the clinical course of the disease. SLE affects the cardiovascular system, the pericardium. 194 Uslu et al Plasma Atherogenic Index and Systemic Lupus Erythematosus endocardium [1,2,3]. Subclinical atherosclerosis and/or related complications in SLE are the most important reasons for the mortality and the morbidity [3, 4]

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