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Hyperuricemia and coronary heart disease mortality: a meta-analysis of prospective cohort studies

BACKGROUND: Hyperuricemia may be associated with an increased risk of coronary heart disease (CHD) mortality; however, the results from prospective studies are conflicting. The objective of this study was to assess the association between hyperuricemia and risk of CHD mortality by performing a meta-...

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Autores principales: Zuo, Tian, Liu, Xuehui, Jiang, Lu, Mao, Shuai, Yin, Xin, Guo, Liheng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5084405/
https://www.ncbi.nlm.nih.gov/pubmed/27793095
http://dx.doi.org/10.1186/s12872-016-0379-z
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author Zuo, Tian
Liu, Xuehui
Jiang, Lu
Mao, Shuai
Yin, Xin
Guo, Liheng
author_facet Zuo, Tian
Liu, Xuehui
Jiang, Lu
Mao, Shuai
Yin, Xin
Guo, Liheng
author_sort Zuo, Tian
collection PubMed
description BACKGROUND: Hyperuricemia may be associated with an increased risk of coronary heart disease (CHD) mortality; however, the results from prospective studies are conflicting. The objective of this study was to assess the association between hyperuricemia and risk of CHD mortality by performing a meta-analysis. METHODS: Pubmed and Embase were searched for relevant prospective cohort studies published until July 2015. Studies were included only if they reported data on CHD mortality related to hyperuricemia in a general population. The pooled adjusted relative risk (RR) was calculated using a random-effects model. RESULTS: A total of 14 studies involving 341 389 adults were identified. Hyperuricemia was associated with an increased risk of CHD mortality (RR: 1.14; 95 % CI: 1.06–1.23) and all-cause mortality (RR: 1.20; 95 % CI: 1.13–1.28). For each increase of 1 mg/dl of serum uric acid (SUA), the overall risks of CHD and all-cause mortality increased by 20 and 9 %, respectively. According to the gender subgroup analyses, hyperuricemia increased the risk of CHD mortality in women (RR: 1.47; 95 % CI: 1.21–1.73) compared to men (RR: 1.10; 95 % CI: 1.00–1.19). The risk of all-cause mortality was greater in women. CONCLUSIONS: Hyperuricemia may modestly increase the risk of CHD and all-cause mortality. Future research is needed to determine whether urate–lowering therapy has beneficial effects for reducing CHD mortality. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12872-016-0379-z) contains supplementary material, which is available to authorized users.
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spelling pubmed-50844052016-10-31 Hyperuricemia and coronary heart disease mortality: a meta-analysis of prospective cohort studies Zuo, Tian Liu, Xuehui Jiang, Lu Mao, Shuai Yin, Xin Guo, Liheng BMC Cardiovasc Disord Research Article BACKGROUND: Hyperuricemia may be associated with an increased risk of coronary heart disease (CHD) mortality; however, the results from prospective studies are conflicting. The objective of this study was to assess the association between hyperuricemia and risk of CHD mortality by performing a meta-analysis. METHODS: Pubmed and Embase were searched for relevant prospective cohort studies published until July 2015. Studies were included only if they reported data on CHD mortality related to hyperuricemia in a general population. The pooled adjusted relative risk (RR) was calculated using a random-effects model. RESULTS: A total of 14 studies involving 341 389 adults were identified. Hyperuricemia was associated with an increased risk of CHD mortality (RR: 1.14; 95 % CI: 1.06–1.23) and all-cause mortality (RR: 1.20; 95 % CI: 1.13–1.28). For each increase of 1 mg/dl of serum uric acid (SUA), the overall risks of CHD and all-cause mortality increased by 20 and 9 %, respectively. According to the gender subgroup analyses, hyperuricemia increased the risk of CHD mortality in women (RR: 1.47; 95 % CI: 1.21–1.73) compared to men (RR: 1.10; 95 % CI: 1.00–1.19). The risk of all-cause mortality was greater in women. CONCLUSIONS: Hyperuricemia may modestly increase the risk of CHD and all-cause mortality. Future research is needed to determine whether urate–lowering therapy has beneficial effects for reducing CHD mortality. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12872-016-0379-z) contains supplementary material, which is available to authorized users. BioMed Central 2016-10-28 /pmc/articles/PMC5084405/ /pubmed/27793095 http://dx.doi.org/10.1186/s12872-016-0379-z Text en © The Author(s). 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Zuo, Tian
Liu, Xuehui
Jiang, Lu
Mao, Shuai
Yin, Xin
Guo, Liheng
Hyperuricemia and coronary heart disease mortality: a meta-analysis of prospective cohort studies
title Hyperuricemia and coronary heart disease mortality: a meta-analysis of prospective cohort studies
title_full Hyperuricemia and coronary heart disease mortality: a meta-analysis of prospective cohort studies
title_fullStr Hyperuricemia and coronary heart disease mortality: a meta-analysis of prospective cohort studies
title_full_unstemmed Hyperuricemia and coronary heart disease mortality: a meta-analysis of prospective cohort studies
title_short Hyperuricemia and coronary heart disease mortality: a meta-analysis of prospective cohort studies
title_sort hyperuricemia and coronary heart disease mortality: a meta-analysis of prospective cohort studies
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5084405/
https://www.ncbi.nlm.nih.gov/pubmed/27793095
http://dx.doi.org/10.1186/s12872-016-0379-z
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