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Clinical Value of Serum Uric Acid in Patients with Suspected Coronary Artery Disease

BACKGROUND/AIMS: Although increased serum uric acid (SUA) concentrations are commonly encountered in patients with risk factors for coronary artery disease (CAD), the clinical value of SUA has not been established. METHODS: The study group comprised 687 consecutive patients with suspected CAD who ha...

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Autores principales: Lim, Hong Euy, Kim, Seong Hwan, Kim, Eung Ju, Kim, Jin Won, Rha, Seung Woon, Seo, Hong Seog, Park, Chang Gyu
Formato: Texto
Lenguaje:English
Publicado: The Korean Association of Internal Medicine 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2829412/
https://www.ncbi.nlm.nih.gov/pubmed/20195399
http://dx.doi.org/10.3904/kjim.2010.25.1.21
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author Lim, Hong Euy
Kim, Seong Hwan
Kim, Eung Ju
Kim, Jin Won
Rha, Seung Woon
Seo, Hong Seog
Park, Chang Gyu
author_facet Lim, Hong Euy
Kim, Seong Hwan
Kim, Eung Ju
Kim, Jin Won
Rha, Seung Woon
Seo, Hong Seog
Park, Chang Gyu
author_sort Lim, Hong Euy
collection PubMed
description BACKGROUND/AIMS: Although increased serum uric acid (SUA) concentrations are commonly encountered in patients with risk factors for coronary artery disease (CAD), the clinical value of SUA has not been established. METHODS: The study group comprised 687 consecutive patients with suspected CAD who had undergone coronary angiography. CAD was defined as stenosis ≥ 50% of the luminal diameter. CAD severity was expressed as 1-, 2-, or 3-vessel disease. Metabolic syndrome (MS) was defined according to National Cholesterol Education Program-Adult Treatment Panel III (NCEP-ATP III) criteria, and aortofemoral pulse wave velocity (PWV) was obtained by arterial catheterization invasively. RESULTS: In total, 395 patients had CAD. SUA was higher in patients with CAD as compared to those without CAD (5.5 ± 1.0 vs. 5.2 ± 1.0 mg/dL, p = 0.004). In addition, SUA was significantly associated with the severity of CAD (p = 0.002). However, after adjusting for significant confounding factors including age, diabetes, smoking, cholesterol, MS, and PWV, SUA was not an independent risk factor for CAD (p = 0.151). Based on a subgroup analysis, SUA was more closely associated with CAD in women than in men, and in the highest quartile (≥ 6.4 mg/dL) than in the first quartile (< 4.8 mg/dL); however, these results were not significant (p = 0.062, p = 0.075, respectively). In a multivariate regression analysis, the most important determinant of SUA was MS (i.e., insulin resistance syndrome), which is strongly associated with CAD. CONCLUSIONS: In patients with suspected CAD, SUA was not an independent risk factor for CAD and may be merely a marker of insulin resistance.
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spelling pubmed-28294122010-03-02 Clinical Value of Serum Uric Acid in Patients with Suspected Coronary Artery Disease Lim, Hong Euy Kim, Seong Hwan Kim, Eung Ju Kim, Jin Won Rha, Seung Woon Seo, Hong Seog Park, Chang Gyu Korean J Intern Med Original Article BACKGROUND/AIMS: Although increased serum uric acid (SUA) concentrations are commonly encountered in patients with risk factors for coronary artery disease (CAD), the clinical value of SUA has not been established. METHODS: The study group comprised 687 consecutive patients with suspected CAD who had undergone coronary angiography. CAD was defined as stenosis ≥ 50% of the luminal diameter. CAD severity was expressed as 1-, 2-, or 3-vessel disease. Metabolic syndrome (MS) was defined according to National Cholesterol Education Program-Adult Treatment Panel III (NCEP-ATP III) criteria, and aortofemoral pulse wave velocity (PWV) was obtained by arterial catheterization invasively. RESULTS: In total, 395 patients had CAD. SUA was higher in patients with CAD as compared to those without CAD (5.5 ± 1.0 vs. 5.2 ± 1.0 mg/dL, p = 0.004). In addition, SUA was significantly associated with the severity of CAD (p = 0.002). However, after adjusting for significant confounding factors including age, diabetes, smoking, cholesterol, MS, and PWV, SUA was not an independent risk factor for CAD (p = 0.151). Based on a subgroup analysis, SUA was more closely associated with CAD in women than in men, and in the highest quartile (≥ 6.4 mg/dL) than in the first quartile (< 4.8 mg/dL); however, these results were not significant (p = 0.062, p = 0.075, respectively). In a multivariate regression analysis, the most important determinant of SUA was MS (i.e., insulin resistance syndrome), which is strongly associated with CAD. CONCLUSIONS: In patients with suspected CAD, SUA was not an independent risk factor for CAD and may be merely a marker of insulin resistance. The Korean Association of Internal Medicine 2010-03 2010-02-26 /pmc/articles/PMC2829412/ /pubmed/20195399 http://dx.doi.org/10.3904/kjim.2010.25.1.21 Text en Copyright © 2010 The Korean Association of Internal Medicine https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (https://creativecommons.org/licenses/by-nc/4.0 (https://creativecommons.org/licenses/by-nc/4.0/) ) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Lim, Hong Euy
Kim, Seong Hwan
Kim, Eung Ju
Kim, Jin Won
Rha, Seung Woon
Seo, Hong Seog
Park, Chang Gyu
Clinical Value of Serum Uric Acid in Patients with Suspected Coronary Artery Disease
title Clinical Value of Serum Uric Acid in Patients with Suspected Coronary Artery Disease
title_full Clinical Value of Serum Uric Acid in Patients with Suspected Coronary Artery Disease
title_fullStr Clinical Value of Serum Uric Acid in Patients with Suspected Coronary Artery Disease
title_full_unstemmed Clinical Value of Serum Uric Acid in Patients with Suspected Coronary Artery Disease
title_short Clinical Value of Serum Uric Acid in Patients with Suspected Coronary Artery Disease
title_sort clinical value of serum uric acid in patients with suspected coronary artery disease
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2829412/
https://www.ncbi.nlm.nih.gov/pubmed/20195399
http://dx.doi.org/10.3904/kjim.2010.25.1.21
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