Literature DB >> 23159203

Uric acid and high sensitive C-reactive protein are associated with subclinical thoracic aortic atherosclerosis.

Mustafa Gür1, Durmuş Yıldıray Sahin, Zafer Elbasan, Gülhan Yüksel Kalkan, Ali Yıldız, Zekeriya Kaya, Betül Özaltun, Murat Çaylı.   

Abstract

BACKGROUND AND
PURPOSE: The detection of atherosclerotic lesions in the aorta by transesophageal echocardiography (TEE) is a marker of diffuse atherosclerotic disease. Hyperuricemia is a well-recognized risk factor for cardiovascular diseases. However, no data are available concerning the relationship between serum uric acid (UA) and subclinical thoracic aortic atherosclerosis. We aimed to investigate the association between thoracic aortic atherosclerosis and serum UA level.
METHODS: We studied 181 patients (mean age 46.3 ± 8 years) who underwent TEE for various indications. Four different grades were determined according to intima-media thickness (IMT) of thoracic aorta. UA and other biochemical markers were measured with an automated chemistry analyzer.
RESULTS: TEE evaluation characterized thoracic aortic intimal morphology as Grade 1 in 69 patients, Grade 2 in 52 patients, Grade 3 in 31 patients, and Grade 4 in 29 patients. The highest UA level was observed in patients with Grade 4 IMT when compared with Grade 1 and 2 IMT groups (p<0.001 and p=0.014, respectively). UA levels in patients with Grade 3 and Grade 2 IMT were also higher than patients with Grade 1 IMT group (p<0.001, for all). In multiple linear regression analysis, IMT was independently associated with UA level (β=0.350, p<0.001), age (β=0.219, p=0.001), total cholesterol (β=-0.212, p=0.031), low-density lipoprotein cholesterol (β=0.350, p=0.001), and high sensitivity C-reactive protein (hsCRP) levels (β=0.148, p=0.014).
CONCLUSION: Uric acid and hsCRP levels are independently and positively associated with subclinical thoracic atherosclerosis.
Copyright © 2012 Japanese College of Cardiology. Published by Elsevier Ltd. All rights reserved.

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Year:  2012        PMID: 23159203     DOI: 10.1016/j.jjcc.2012.08.023

Source DB:  PubMed          Journal:  J Cardiol        ISSN: 0914-5087            Impact factor:   3.159


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