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Effect of hyperuricemia and treatment for hyperuricemia in Japanese hemodialysis patients: A cohort study

Whether higher serum uric acid (UA) values comprise a risk factor for death and whether treatment for high UA is effective in patients undergoing hemodialysis (HD) are essentially unknown. To determine associations between UA and all-cause or cardiovascular (CV) mortality, interactions between UA or...

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Autores principales: Sugano, Naoki, Maruyama, Yukio, Kidoguchi, Satoshi, Ohno, Iwao, Wada, Atsushi, Shigematsu, Takashi, Masakane, Ikuto, Yokoo, Takashi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6553731/
https://www.ncbi.nlm.nih.gov/pubmed/31170241
http://dx.doi.org/10.1371/journal.pone.0217859
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author Sugano, Naoki
Maruyama, Yukio
Kidoguchi, Satoshi
Ohno, Iwao
Wada, Atsushi
Shigematsu, Takashi
Masakane, Ikuto
Yokoo, Takashi
author_facet Sugano, Naoki
Maruyama, Yukio
Kidoguchi, Satoshi
Ohno, Iwao
Wada, Atsushi
Shigematsu, Takashi
Masakane, Ikuto
Yokoo, Takashi
author_sort Sugano, Naoki
collection PubMed
description Whether higher serum uric acid (UA) values comprise a risk factor for death and whether treatment for high UA is effective in patients undergoing hemodialysis (HD) are essentially unknown. To determine associations between UA and all-cause or cardiovascular (CV) mortality, interactions between UA or medication and effects on mortality, and significance of treatment for hyperuricemia in patients undergoing hemodialysis (HD). We collected the baseline data of 222,434 patients undergoing three HD sessions per week, extracted from a nationwide dialysis registry at the end of 2011 in Japan. Then we evaluated the interaction between serum uric acid level and all-cause and cardiovascular (CV) mortality by the end of 2012. Univariate and multivariate logistic regression and Cox regression analyses found higher all-cause and CV mortality rates among patients with lower, than higher UA values. Hazard ratios (HR) for all-cause and CV mortality were significantly lower in a group with, than without medication for hyperuricemia (HR, 0.837; 95% confidence interval (CI), 0.789–0.889 and HR, 0.830; 95%CI 0.758–0.909, respectively). Lower UA values remained associated with all-cause and CV mortality rates even when in patients taking medication for hyperuricemia. The chief interacting factors for higher mortality rates due to lower UA were higher BMI and diabetes mellitus. In conclusion, lower UA levels were independently associated with higher all-cause and CV mortality among Japanese patients undergoing HD. Intervention for hyperuricemia is considered to improve patient outcomes.
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spelling pubmed-65537312019-06-17 Effect of hyperuricemia and treatment for hyperuricemia in Japanese hemodialysis patients: A cohort study Sugano, Naoki Maruyama, Yukio Kidoguchi, Satoshi Ohno, Iwao Wada, Atsushi Shigematsu, Takashi Masakane, Ikuto Yokoo, Takashi PLoS One Research Article Whether higher serum uric acid (UA) values comprise a risk factor for death and whether treatment for high UA is effective in patients undergoing hemodialysis (HD) are essentially unknown. To determine associations between UA and all-cause or cardiovascular (CV) mortality, interactions between UA or medication and effects on mortality, and significance of treatment for hyperuricemia in patients undergoing hemodialysis (HD). We collected the baseline data of 222,434 patients undergoing three HD sessions per week, extracted from a nationwide dialysis registry at the end of 2011 in Japan. Then we evaluated the interaction between serum uric acid level and all-cause and cardiovascular (CV) mortality by the end of 2012. Univariate and multivariate logistic regression and Cox regression analyses found higher all-cause and CV mortality rates among patients with lower, than higher UA values. Hazard ratios (HR) for all-cause and CV mortality were significantly lower in a group with, than without medication for hyperuricemia (HR, 0.837; 95% confidence interval (CI), 0.789–0.889 and HR, 0.830; 95%CI 0.758–0.909, respectively). Lower UA values remained associated with all-cause and CV mortality rates even when in patients taking medication for hyperuricemia. The chief interacting factors for higher mortality rates due to lower UA were higher BMI and diabetes mellitus. In conclusion, lower UA levels were independently associated with higher all-cause and CV mortality among Japanese patients undergoing HD. Intervention for hyperuricemia is considered to improve patient outcomes. Public Library of Science 2019-06-06 /pmc/articles/PMC6553731/ /pubmed/31170241 http://dx.doi.org/10.1371/journal.pone.0217859 Text en © 2019 Sugano et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Sugano, Naoki
Maruyama, Yukio
Kidoguchi, Satoshi
Ohno, Iwao
Wada, Atsushi
Shigematsu, Takashi
Masakane, Ikuto
Yokoo, Takashi
Effect of hyperuricemia and treatment for hyperuricemia in Japanese hemodialysis patients: A cohort study
title Effect of hyperuricemia and treatment for hyperuricemia in Japanese hemodialysis patients: A cohort study
title_full Effect of hyperuricemia and treatment for hyperuricemia in Japanese hemodialysis patients: A cohort study
title_fullStr Effect of hyperuricemia and treatment for hyperuricemia in Japanese hemodialysis patients: A cohort study
title_full_unstemmed Effect of hyperuricemia and treatment for hyperuricemia in Japanese hemodialysis patients: A cohort study
title_short Effect of hyperuricemia and treatment for hyperuricemia in Japanese hemodialysis patients: A cohort study
title_sort effect of hyperuricemia and treatment for hyperuricemia in japanese hemodialysis patients: a cohort study
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6553731/
https://www.ncbi.nlm.nih.gov/pubmed/31170241
http://dx.doi.org/10.1371/journal.pone.0217859
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