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Association of Serum Total Bilirubin with Serum High Sensitivity C-reactive Protein in Middle-aged Men

BACKGROUND: It has been suggested that bilirubin has an inverse association with cardiovascular disease (CVD) due to its antioxidant properties. However, there are few data regarding the relationship between serum total bilirubin (sTB) and risk factors for CVD in Koreans. This study aimed to evaluat...

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Autores principales: Yu, Kiwoong, Kim, Cheolhwan, Sung, Eunju, Shin, Hocheol, Lee, Hyewon
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Academy of Family Medicine 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3383147/
https://www.ncbi.nlm.nih.gov/pubmed/22745870
http://dx.doi.org/10.4082/kjfm.2011.32.6.327
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author Yu, Kiwoong
Kim, Cheolhwan
Sung, Eunju
Shin, Hocheol
Lee, Hyewon
author_facet Yu, Kiwoong
Kim, Cheolhwan
Sung, Eunju
Shin, Hocheol
Lee, Hyewon
author_sort Yu, Kiwoong
collection PubMed
description BACKGROUND: It has been suggested that bilirubin has an inverse association with cardiovascular disease (CVD) due to its antioxidant properties. However, there are few data regarding the relationship between serum total bilirubin (sTB) and risk factors for CVD in Koreans. This study aimed to evaluate the relationship between sTB and high sensitivity C-reactive protein (hsCRP), which is an independent risk factor for CVD. METHODS: We performed a cross sectional study in 6,800 men who were examined at a health promotion center at a university hospital in Korea between May 2005 and June 2006. We grouped the subjects according to values of serum hsCRP (above or below 1.0 mg/L) and compared the characteristics of the two groups. To evaluate the relationship between sTB and hsCRP, we classified the subjects according to quartile values of sTB. Multivariate logistic regression analyses were used to analyze the relationship of levels of sTB and hsCRP after adjusting for known risk factors for CVD. RESULTS: Serum hsCRP was significantly associated with body mass index (BMI), smoking, diabetes, hypertension, fasting plasma glucose, systolic blood pressure, alanine aminotransferase, and total cholesterol/high density lipoprotein (TC/HDL-C) ratio, but not with age or alcohol use. As levels of sTB increased, there was a decrease in age, numbers of smokers, BMI, and TC/HDL ratio. Compared to the lowest quartile of sTB, levels of hsCRP decreased with odds ratios of 0.82 (95% CI, 0.71 to 0.96), 0.75 (95% CI, 0.65 to 0.88), and 0.63 (95% CI, 0.54 to 0.74) in the 2nd, 3rd, and 4th quartiles of bilirubin, respectively. CONCLUSION: Bilirubin may be inversely associated with hsCRP
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spelling pubmed-33831472012-06-28 Association of Serum Total Bilirubin with Serum High Sensitivity C-reactive Protein in Middle-aged Men Yu, Kiwoong Kim, Cheolhwan Sung, Eunju Shin, Hocheol Lee, Hyewon Korean J Fam Med Original Article BACKGROUND: It has been suggested that bilirubin has an inverse association with cardiovascular disease (CVD) due to its antioxidant properties. However, there are few data regarding the relationship between serum total bilirubin (sTB) and risk factors for CVD in Koreans. This study aimed to evaluate the relationship between sTB and high sensitivity C-reactive protein (hsCRP), which is an independent risk factor for CVD. METHODS: We performed a cross sectional study in 6,800 men who were examined at a health promotion center at a university hospital in Korea between May 2005 and June 2006. We grouped the subjects according to values of serum hsCRP (above or below 1.0 mg/L) and compared the characteristics of the two groups. To evaluate the relationship between sTB and hsCRP, we classified the subjects according to quartile values of sTB. Multivariate logistic regression analyses were used to analyze the relationship of levels of sTB and hsCRP after adjusting for known risk factors for CVD. RESULTS: Serum hsCRP was significantly associated with body mass index (BMI), smoking, diabetes, hypertension, fasting plasma glucose, systolic blood pressure, alanine aminotransferase, and total cholesterol/high density lipoprotein (TC/HDL-C) ratio, but not with age or alcohol use. As levels of sTB increased, there was a decrease in age, numbers of smokers, BMI, and TC/HDL ratio. Compared to the lowest quartile of sTB, levels of hsCRP decreased with odds ratios of 0.82 (95% CI, 0.71 to 0.96), 0.75 (95% CI, 0.65 to 0.88), and 0.63 (95% CI, 0.54 to 0.74) in the 2nd, 3rd, and 4th quartiles of bilirubin, respectively. CONCLUSION: Bilirubin may be inversely associated with hsCRP The Korean Academy of Family Medicine 2011-09 2011-09-28 /pmc/articles/PMC3383147/ /pubmed/22745870 http://dx.doi.org/10.4082/kjfm.2011.32.6.327 Text en Copyright © 2011 The Korean Academy of Family Medicine http://creativecommons.org/licenses/by-nc/3.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Yu, Kiwoong
Kim, Cheolhwan
Sung, Eunju
Shin, Hocheol
Lee, Hyewon
Association of Serum Total Bilirubin with Serum High Sensitivity C-reactive Protein in Middle-aged Men
title Association of Serum Total Bilirubin with Serum High Sensitivity C-reactive Protein in Middle-aged Men
title_full Association of Serum Total Bilirubin with Serum High Sensitivity C-reactive Protein in Middle-aged Men
title_fullStr Association of Serum Total Bilirubin with Serum High Sensitivity C-reactive Protein in Middle-aged Men
title_full_unstemmed Association of Serum Total Bilirubin with Serum High Sensitivity C-reactive Protein in Middle-aged Men
title_short Association of Serum Total Bilirubin with Serum High Sensitivity C-reactive Protein in Middle-aged Men
title_sort association of serum total bilirubin with serum high sensitivity c-reactive protein in middle-aged men
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3383147/
https://www.ncbi.nlm.nih.gov/pubmed/22745870
http://dx.doi.org/10.4082/kjfm.2011.32.6.327
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