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Serum Uric Acid as an Independent Risk Factor for the Presence and Severity of Early-Onset Coronary Artery Disease: A Case-Control Study

Serum uric acid (UA) is the final product of purine metabolism in humans. The present study is aimed at identifying the potential association between serum UA and early-onset coronary artery disease (EOCAD). The study population consisted of 1093 EOCAD patients aged ≤50 years, and 1117 age- and sex-...

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Autores principales: Tian, Ting-Ting, Li, Hui, Chen, Sheng-Jie, Wang, Qing, Tian, Qing-Wu, Zhang, Bei-Bei, Zhu, Jie, He, Guo-Wei, Lun, Li-Min, Xuan, Chao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6218741/
https://www.ncbi.nlm.nih.gov/pubmed/30425752
http://dx.doi.org/10.1155/2018/1236837
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author Tian, Ting-Ting
Li, Hui
Chen, Sheng-Jie
Wang, Qing
Tian, Qing-Wu
Zhang, Bei-Bei
Zhu, Jie
He, Guo-Wei
Lun, Li-Min
Xuan, Chao
author_facet Tian, Ting-Ting
Li, Hui
Chen, Sheng-Jie
Wang, Qing
Tian, Qing-Wu
Zhang, Bei-Bei
Zhu, Jie
He, Guo-Wei
Lun, Li-Min
Xuan, Chao
author_sort Tian, Ting-Ting
collection PubMed
description Serum uric acid (UA) is the final product of purine metabolism in humans. The present study is aimed at identifying the potential association between serum UA and early-onset coronary artery disease (EOCAD). The study population consisted of 1093 EOCAD patients aged ≤50 years, and 1117 age- and sex-matched apparently healthy people served as controls. The concentrations of UA were measured by uricase method. The severity of CAD was evaluated by Gensini score. The mean serum level of UA was 5.843 ± 1.479 mg/dl in EOCAD patients and 5.433 ± 1.529 mg/dl in controls. Serum UA levels were significantly higher in the EOCAD group than those in the control group (P < 0.001) and was an independent risk factor for EOCAD (OR = 1.100, 95% CI: 1.022–1.185). The early-onset myocardial infarction patients with 3-vessel disease had higher serum UA levels than those with 1- or 2-vessel disease. The serum UA levels of EOCAD patients with acute coronary syndrome were significantly higher than those with chronic coronary artery disease. EOCAD patients with hyperuricemia had higher Gensini scores than those without hyperuricemia. In addition, the serum UA levels were affected by drinking (P < 0.01) and were positively correlated with serum creatinine (r = 0.323) and weight (r = 0.327). Our results show that serum UA was an independent risk factor for EOCAD. The serum UA levels were associated with the presence and severity of EOCAD and suggested that UA may be involved in the progression of EOCAD.
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spelling pubmed-62187412018-11-13 Serum Uric Acid as an Independent Risk Factor for the Presence and Severity of Early-Onset Coronary Artery Disease: A Case-Control Study Tian, Ting-Ting Li, Hui Chen, Sheng-Jie Wang, Qing Tian, Qing-Wu Zhang, Bei-Bei Zhu, Jie He, Guo-Wei Lun, Li-Min Xuan, Chao Dis Markers Research Article Serum uric acid (UA) is the final product of purine metabolism in humans. The present study is aimed at identifying the potential association between serum UA and early-onset coronary artery disease (EOCAD). The study population consisted of 1093 EOCAD patients aged ≤50 years, and 1117 age- and sex-matched apparently healthy people served as controls. The concentrations of UA were measured by uricase method. The severity of CAD was evaluated by Gensini score. The mean serum level of UA was 5.843 ± 1.479 mg/dl in EOCAD patients and 5.433 ± 1.529 mg/dl in controls. Serum UA levels were significantly higher in the EOCAD group than those in the control group (P < 0.001) and was an independent risk factor for EOCAD (OR = 1.100, 95% CI: 1.022–1.185). The early-onset myocardial infarction patients with 3-vessel disease had higher serum UA levels than those with 1- or 2-vessel disease. The serum UA levels of EOCAD patients with acute coronary syndrome were significantly higher than those with chronic coronary artery disease. EOCAD patients with hyperuricemia had higher Gensini scores than those without hyperuricemia. In addition, the serum UA levels were affected by drinking (P < 0.01) and were positively correlated with serum creatinine (r = 0.323) and weight (r = 0.327). Our results show that serum UA was an independent risk factor for EOCAD. The serum UA levels were associated with the presence and severity of EOCAD and suggested that UA may be involved in the progression of EOCAD. Hindawi 2018-10-23 /pmc/articles/PMC6218741/ /pubmed/30425752 http://dx.doi.org/10.1155/2018/1236837 Text en Copyright © 2018 Ting-Ting Tian et al. http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Tian, Ting-Ting
Li, Hui
Chen, Sheng-Jie
Wang, Qing
Tian, Qing-Wu
Zhang, Bei-Bei
Zhu, Jie
He, Guo-Wei
Lun, Li-Min
Xuan, Chao
Serum Uric Acid as an Independent Risk Factor for the Presence and Severity of Early-Onset Coronary Artery Disease: A Case-Control Study
title Serum Uric Acid as an Independent Risk Factor for the Presence and Severity of Early-Onset Coronary Artery Disease: A Case-Control Study
title_full Serum Uric Acid as an Independent Risk Factor for the Presence and Severity of Early-Onset Coronary Artery Disease: A Case-Control Study
title_fullStr Serum Uric Acid as an Independent Risk Factor for the Presence and Severity of Early-Onset Coronary Artery Disease: A Case-Control Study
title_full_unstemmed Serum Uric Acid as an Independent Risk Factor for the Presence and Severity of Early-Onset Coronary Artery Disease: A Case-Control Study
title_short Serum Uric Acid as an Independent Risk Factor for the Presence and Severity of Early-Onset Coronary Artery Disease: A Case-Control Study
title_sort serum uric acid as an independent risk factor for the presence and severity of early-onset coronary artery disease: a case-control study
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6218741/
https://www.ncbi.nlm.nih.gov/pubmed/30425752
http://dx.doi.org/10.1155/2018/1236837
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