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Uric acid is an independent risk factor for carotid atherosclerosis in a Japanese elderly population without metabolic syndrome

BACKGROUND: Carotid intima-media thickness (IMT) is an useful surrogate marker of cardiovascular disease. Associations between uric acid (UA), metabolic syndrome (MetS) and carotid IMT have been reported, but findings regarding the relationship have been inconsistent. METHODS: A total of 1,579 Japan...

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Autores principales: Takayama, Shuzo, Kawamoto, Ryuichi, Kusunoki, Tomo, Abe, Masanori, Onji, Morikazu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3293733/
https://www.ncbi.nlm.nih.gov/pubmed/22234039
http://dx.doi.org/10.1186/1475-2840-11-2
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author Takayama, Shuzo
Kawamoto, Ryuichi
Kusunoki, Tomo
Abe, Masanori
Onji, Morikazu
author_facet Takayama, Shuzo
Kawamoto, Ryuichi
Kusunoki, Tomo
Abe, Masanori
Onji, Morikazu
author_sort Takayama, Shuzo
collection PubMed
description BACKGROUND: Carotid intima-media thickness (IMT) is an useful surrogate marker of cardiovascular disease. Associations between uric acid (UA), metabolic syndrome (MetS) and carotid IMT have been reported, but findings regarding the relationship have been inconsistent. METHODS: A total of 1,579 Japanese elderly subjects aged ≥65 years {663 men aged, 78 ± 8 (mean ± standard deviation) years and 916 women aged 79 ± 8 years} were divided into 4 groups according to UA quartiles. We first investigated the association between UA concentrations and confounding factors including MetS; then, we assessed whether there is an independent association of UA with carotid IMT and atherosclerosis in participants subdivided according to gender and MetS status. RESULTS: Carotid IMT was significantly increased according to the quartiles of UA in both genders without MetS and women with MetS. Multivariate logistic regression analysis showed that odds ratio (OR) {95% confidence interval (CI)} in men for carotid atherosclerosis was significantly increased in the third (OR, 1.75; 95% CI, 1.02-3.02), and fourth quartiles (OR, 2.01; 95% CI, 1.12-3.60) of UA compared with that in the first quartile of UA, and the OR in women was significantly increased in the fourth quartile (OR, 2.10; 95% CI, 1.30-3.39). Similarly, the ORs were significantly associated with increasing quartiles of UA in both genders without MetS, but not necessarily increased in those with MetS. CONCLUSIONS: UA was found to be an independent risk factor for incidence of carotid atherosclerosis in both genders without MetS.
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spelling pubmed-32937332012-03-06 Uric acid is an independent risk factor for carotid atherosclerosis in a Japanese elderly population without metabolic syndrome Takayama, Shuzo Kawamoto, Ryuichi Kusunoki, Tomo Abe, Masanori Onji, Morikazu Cardiovasc Diabetol Original Investigation BACKGROUND: Carotid intima-media thickness (IMT) is an useful surrogate marker of cardiovascular disease. Associations between uric acid (UA), metabolic syndrome (MetS) and carotid IMT have been reported, but findings regarding the relationship have been inconsistent. METHODS: A total of 1,579 Japanese elderly subjects aged ≥65 years {663 men aged, 78 ± 8 (mean ± standard deviation) years and 916 women aged 79 ± 8 years} were divided into 4 groups according to UA quartiles. We first investigated the association between UA concentrations and confounding factors including MetS; then, we assessed whether there is an independent association of UA with carotid IMT and atherosclerosis in participants subdivided according to gender and MetS status. RESULTS: Carotid IMT was significantly increased according to the quartiles of UA in both genders without MetS and women with MetS. Multivariate logistic regression analysis showed that odds ratio (OR) {95% confidence interval (CI)} in men for carotid atherosclerosis was significantly increased in the third (OR, 1.75; 95% CI, 1.02-3.02), and fourth quartiles (OR, 2.01; 95% CI, 1.12-3.60) of UA compared with that in the first quartile of UA, and the OR in women was significantly increased in the fourth quartile (OR, 2.10; 95% CI, 1.30-3.39). Similarly, the ORs were significantly associated with increasing quartiles of UA in both genders without MetS, but not necessarily increased in those with MetS. CONCLUSIONS: UA was found to be an independent risk factor for incidence of carotid atherosclerosis in both genders without MetS. BioMed Central 2012-01-10 /pmc/articles/PMC3293733/ /pubmed/22234039 http://dx.doi.org/10.1186/1475-2840-11-2 Text en Copyright ©2012 Takayama et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Investigation
Takayama, Shuzo
Kawamoto, Ryuichi
Kusunoki, Tomo
Abe, Masanori
Onji, Morikazu
Uric acid is an independent risk factor for carotid atherosclerosis in a Japanese elderly population without metabolic syndrome
title Uric acid is an independent risk factor for carotid atherosclerosis in a Japanese elderly population without metabolic syndrome
title_full Uric acid is an independent risk factor for carotid atherosclerosis in a Japanese elderly population without metabolic syndrome
title_fullStr Uric acid is an independent risk factor for carotid atherosclerosis in a Japanese elderly population without metabolic syndrome
title_full_unstemmed Uric acid is an independent risk factor for carotid atherosclerosis in a Japanese elderly population without metabolic syndrome
title_short Uric acid is an independent risk factor for carotid atherosclerosis in a Japanese elderly population without metabolic syndrome
title_sort uric acid is an independent risk factor for carotid atherosclerosis in a japanese elderly population without metabolic syndrome
topic Original Investigation
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3293733/
https://www.ncbi.nlm.nih.gov/pubmed/22234039
http://dx.doi.org/10.1186/1475-2840-11-2
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