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The Protective Effects of Increasing Serum Uric Acid Level on Development of Metabolic Syndrome

BACKGROUND: It has not been determined whether changes in serum uric acid (SUA) level are associated with incident metabolic syndrome (MetS). The aim of the current study was to investigate the relationship between changes in SUA level and development of MetS in a large number of subjects. METHODS:...

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Autores principales: Yu, Tae Yang, Jin, Sang-Man, Jee, Jae Hwan, Bae, Ji Cheol, Lee, Moon-Kyu, Kim, Jae Hyeon
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Diabetes Association 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6712225/
https://www.ncbi.nlm.nih.gov/pubmed/30877704
http://dx.doi.org/10.4093/dmj.2018.0079
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author Yu, Tae Yang
Jin, Sang-Man
Jee, Jae Hwan
Bae, Ji Cheol
Lee, Moon-Kyu
Kim, Jae Hyeon
author_facet Yu, Tae Yang
Jin, Sang-Man
Jee, Jae Hwan
Bae, Ji Cheol
Lee, Moon-Kyu
Kim, Jae Hyeon
author_sort Yu, Tae Yang
collection PubMed
description BACKGROUND: It has not been determined whether changes in serum uric acid (SUA) level are associated with incident metabolic syndrome (MetS). The aim of the current study was to investigate the relationship between changes in SUA level and development of MetS in a large number of subjects. METHODS: In total, 13,057 subjects participating in a medical health check-up program without a diagnosis of MetS at baseline were enrolled. Cox proportional hazards models were used to test the independent association of percent changes in SUA level with development of MetS. RESULTS: After adjustment for age, systolic blood pressure, body mass index, fat-free mass (%), estimated glomerular filtration rate, smoking status, fasting glucose, triglyceride, low density lipoprotein cholesterol, high density lipoprotein cholesterol, and baseline SUA levels, the hazard ratios (HRs) (95% confidence intervals [CIs]) for incident MetS in the second, third, and fourth quartiles compared to the first quartile of percent change in SUA level were 1.055 (0.936 to 1.190), 0.927 (0.818 to 1.050), and 0.807 (0.707 to 0.922) in male (P for trend <0.001) and 1.000 (0.843 to 1.186), 0.744 (0.615 to 0.900), and 0.684 (0.557 to 0.840) in female (P for trend <0.001), respectively. As a continuous variable in the fully-adjusted model, each one-standard deviation increase in percent change in SUA level was associated with an HR (95% CI) for incident MetS of 0.944 (0.906 to 0.982) in male (P=0.005) and 0.851 (0.801 to 0.905) in female (P<0.001). CONCLUSION: The current study demonstrated that increasing SUA level independently protected against the development of MetS, suggesting a possible role of SUA as an antioxidant in the pathogenesis of incident MetS.
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spelling pubmed-67122252019-09-04 The Protective Effects of Increasing Serum Uric Acid Level on Development of Metabolic Syndrome Yu, Tae Yang Jin, Sang-Man Jee, Jae Hwan Bae, Ji Cheol Lee, Moon-Kyu Kim, Jae Hyeon Diabetes Metab J Original Article BACKGROUND: It has not been determined whether changes in serum uric acid (SUA) level are associated with incident metabolic syndrome (MetS). The aim of the current study was to investigate the relationship between changes in SUA level and development of MetS in a large number of subjects. METHODS: In total, 13,057 subjects participating in a medical health check-up program without a diagnosis of MetS at baseline were enrolled. Cox proportional hazards models were used to test the independent association of percent changes in SUA level with development of MetS. RESULTS: After adjustment for age, systolic blood pressure, body mass index, fat-free mass (%), estimated glomerular filtration rate, smoking status, fasting glucose, triglyceride, low density lipoprotein cholesterol, high density lipoprotein cholesterol, and baseline SUA levels, the hazard ratios (HRs) (95% confidence intervals [CIs]) for incident MetS in the second, third, and fourth quartiles compared to the first quartile of percent change in SUA level were 1.055 (0.936 to 1.190), 0.927 (0.818 to 1.050), and 0.807 (0.707 to 0.922) in male (P for trend <0.001) and 1.000 (0.843 to 1.186), 0.744 (0.615 to 0.900), and 0.684 (0.557 to 0.840) in female (P for trend <0.001), respectively. As a continuous variable in the fully-adjusted model, each one-standard deviation increase in percent change in SUA level was associated with an HR (95% CI) for incident MetS of 0.944 (0.906 to 0.982) in male (P=0.005) and 0.851 (0.801 to 0.905) in female (P<0.001). CONCLUSION: The current study demonstrated that increasing SUA level independently protected against the development of MetS, suggesting a possible role of SUA as an antioxidant in the pathogenesis of incident MetS. Korean Diabetes Association 2019-08 2019-02-21 /pmc/articles/PMC6712225/ /pubmed/30877704 http://dx.doi.org/10.4093/dmj.2018.0079 Text en Copyright © 2019 Korean Diabetes Association http://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 (http://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
Yu, Tae Yang
Jin, Sang-Man
Jee, Jae Hwan
Bae, Ji Cheol
Lee, Moon-Kyu
Kim, Jae Hyeon
The Protective Effects of Increasing Serum Uric Acid Level on Development of Metabolic Syndrome
title The Protective Effects of Increasing Serum Uric Acid Level on Development of Metabolic Syndrome
title_full The Protective Effects of Increasing Serum Uric Acid Level on Development of Metabolic Syndrome
title_fullStr The Protective Effects of Increasing Serum Uric Acid Level on Development of Metabolic Syndrome
title_full_unstemmed The Protective Effects of Increasing Serum Uric Acid Level on Development of Metabolic Syndrome
title_short The Protective Effects of Increasing Serum Uric Acid Level on Development of Metabolic Syndrome
title_sort protective effects of increasing serum uric acid level on development of metabolic syndrome
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6712225/
https://www.ncbi.nlm.nih.gov/pubmed/30877704
http://dx.doi.org/10.4093/dmj.2018.0079
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