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Relationship between serum bilirubin levels and mortality in patients on peritoneal dialysis

Background: Studies have shown that the serum total bilirubin (TBil) is associated with the mortality of the general population and of hemodialysis patients. However, few studies have examined the associations of the direct bilirubin (DBil) and indirect bilirubin (IBil) with the mortality of periton...

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Autores principales: Zhan, Xiaojiang, Yang, Mei, Chen, Yanbing, Yan, Caixia, Wang, Yifan, Zhao, Qing, Chen, Qinkai, Zhang, Li
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6598530/
https://www.ncbi.nlm.nih.gov/pubmed/31240974
http://dx.doi.org/10.1080/0886022X.2019.1628062
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author Zhan, Xiaojiang
Yang, Mei
Chen, Yanbing
Yan, Caixia
Wang, Yifan
Zhao, Qing
Chen, Qinkai
Zhang, Li
author_facet Zhan, Xiaojiang
Yang, Mei
Chen, Yanbing
Yan, Caixia
Wang, Yifan
Zhao, Qing
Chen, Qinkai
Zhang, Li
author_sort Zhan, Xiaojiang
collection PubMed
description Background: Studies have shown that the serum total bilirubin (TBil) is associated with the mortality of the general population and of hemodialysis patients. However, few studies have examined the associations of the direct bilirubin (DBil) and indirect bilirubin (IBil) with the mortality of peritoneal dialysis (PD) patients. Methods: This was a retrospective cohort study. Clinical and laboratory data were collected from 740 PD patients. The primary endpoint was 5-year all-cause mortality. Survival analysis was performed using the Kaplan–Meier method with the log-rank test. The mortality hazard ratio was evaluated using Cox regression models. Results: Among the 740 PD patients, the mean age was 49.9 ± 15.0 years, 54.9% were men, and 20.3% had diabetes. During the median follow-up period of 28 months (interquartile range, 14–41 months), 178 patients died. Kaplan–Meier analysis revealed that all-cause mortality was higher in the patients in the higher TBil group than in the lower TBil group (25.6% vs. 18.3%, p = .017) and in patients in the higher IBil group than in the lower IBil group (24.3% vs. 19%, p = .026). Multivariate analysis showed that compared with the lower TBil group, the 5-year mortality risk was higher in the higher TBil group (HR = 1.69, 95% CI: 1.11–2.56, p = .014). Similarly, there was a 56% higher risk of 5-year mortality in the higher IBil group than in the lower IBil group (HR = 1.56, 95% CI: 1.04–2.34, p = .032). However, no such associations were observed between the DBil and the mortality risk. Conclusions: The baseline serum TBil and IBil levels were significantly associated with 5-year all-cause mortality among PD patients.
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spelling pubmed-65985302019-07-03 Relationship between serum bilirubin levels and mortality in patients on peritoneal dialysis Zhan, Xiaojiang Yang, Mei Chen, Yanbing Yan, Caixia Wang, Yifan Zhao, Qing Chen, Qinkai Zhang, Li Ren Fail Clinical Study Background: Studies have shown that the serum total bilirubin (TBil) is associated with the mortality of the general population and of hemodialysis patients. However, few studies have examined the associations of the direct bilirubin (DBil) and indirect bilirubin (IBil) with the mortality of peritoneal dialysis (PD) patients. Methods: This was a retrospective cohort study. Clinical and laboratory data were collected from 740 PD patients. The primary endpoint was 5-year all-cause mortality. Survival analysis was performed using the Kaplan–Meier method with the log-rank test. The mortality hazard ratio was evaluated using Cox regression models. Results: Among the 740 PD patients, the mean age was 49.9 ± 15.0 years, 54.9% were men, and 20.3% had diabetes. During the median follow-up period of 28 months (interquartile range, 14–41 months), 178 patients died. Kaplan–Meier analysis revealed that all-cause mortality was higher in the patients in the higher TBil group than in the lower TBil group (25.6% vs. 18.3%, p = .017) and in patients in the higher IBil group than in the lower IBil group (24.3% vs. 19%, p = .026). Multivariate analysis showed that compared with the lower TBil group, the 5-year mortality risk was higher in the higher TBil group (HR = 1.69, 95% CI: 1.11–2.56, p = .014). Similarly, there was a 56% higher risk of 5-year mortality in the higher IBil group than in the lower IBil group (HR = 1.56, 95% CI: 1.04–2.34, p = .032). However, no such associations were observed between the DBil and the mortality risk. Conclusions: The baseline serum TBil and IBil levels were significantly associated with 5-year all-cause mortality among PD patients. Taylor & Francis 2019-06-26 /pmc/articles/PMC6598530/ /pubmed/31240974 http://dx.doi.org/10.1080/0886022X.2019.1628062 Text en © 2019 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. 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 work is properly cited.
spellingShingle Clinical Study
Zhan, Xiaojiang
Yang, Mei
Chen, Yanbing
Yan, Caixia
Wang, Yifan
Zhao, Qing
Chen, Qinkai
Zhang, Li
Relationship between serum bilirubin levels and mortality in patients on peritoneal dialysis
title Relationship between serum bilirubin levels and mortality in patients on peritoneal dialysis
title_full Relationship between serum bilirubin levels and mortality in patients on peritoneal dialysis
title_fullStr Relationship between serum bilirubin levels and mortality in patients on peritoneal dialysis
title_full_unstemmed Relationship between serum bilirubin levels and mortality in patients on peritoneal dialysis
title_short Relationship between serum bilirubin levels and mortality in patients on peritoneal dialysis
title_sort relationship between serum bilirubin levels and mortality in patients on peritoneal dialysis
topic Clinical Study
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6598530/
https://www.ncbi.nlm.nih.gov/pubmed/31240974
http://dx.doi.org/10.1080/0886022X.2019.1628062
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