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Serum Bilirubin Is Correlated With the Progression of IgA Vasculitis With Nephritis

Background: Bilirubin has been identified as an endogenous antioxidant and cellular protectant. The present study was performed to clarify the potential influence of serum bilirubin on IgA vasculitis with nephritis (IgAV-N). Methods: One hundred and eighty-nine IgAV-N patients over 14 years old were...

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Autores principales: Tan, Jiaxing, Pei, Gaiqin, Xu, Yicong, Hu, Tengyue, Tan, Li, Zhong, Zhengxia, Tarun, Padamata, Tang, Yi, Qin, Wei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8217633/
https://www.ncbi.nlm.nih.gov/pubmed/34169080
http://dx.doi.org/10.3389/fmed.2021.596151
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author Tan, Jiaxing
Pei, Gaiqin
Xu, Yicong
Hu, Tengyue
Tan, Li
Zhong, Zhengxia
Tarun, Padamata
Tang, Yi
Qin, Wei
author_facet Tan, Jiaxing
Pei, Gaiqin
Xu, Yicong
Hu, Tengyue
Tan, Li
Zhong, Zhengxia
Tarun, Padamata
Tang, Yi
Qin, Wei
author_sort Tan, Jiaxing
collection PubMed
description Background: Bilirubin has been identified as an endogenous antioxidant and cellular protectant. The present study was performed to clarify the potential influence of serum bilirubin on IgA vasculitis with nephritis (IgAV-N). Methods: One hundred and eighty-nine IgAV-N patients over 14 years old were enrolled. The patients were divided into two groups by the optimum cut-off value calculated by ROC curve. The composite endpoints were defined as a 60% decline in estimate glomerular filtration rate (e-GFR), end-stage renal disease (ESRD) and/or death. Kaplan-Meier (K-M) analysis and multivariate Cox analysis were carried out to determine the predictors for renal outcomes. In order to eliminate the influence of different baseline data, a 1:2 propensity score (PS) match was performed to make the results comparable and convictive. Results: The baseline data suggested that patients in low serum bilirubin group had significantly higher levels of systolic blood pressure, proteinuria, serum creatinine and crescent formation ratio and lower levels of serum albumin and hemoglobin. Renal survival analysis indicated that lower serum bilirubin levels were significantly correlated with a poorer prognosis. Multivariate Cox analysis demonstrated that the higher level of serum bilirubin was an independent protective factor for renal survival (HR, 0.172; 95% CI, 0.030–0.991; P = 0.049). After PS matching, the baseline characters of two groups had no statistical differences. Similar outcomes were demonstrated in K-M curve and the multivariate Cox analysis. Conclusion: Elevated bilirubin levels might be related to the favorable renal outcomes.
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spelling pubmed-82176332021-06-23 Serum Bilirubin Is Correlated With the Progression of IgA Vasculitis With Nephritis Tan, Jiaxing Pei, Gaiqin Xu, Yicong Hu, Tengyue Tan, Li Zhong, Zhengxia Tarun, Padamata Tang, Yi Qin, Wei Front Med (Lausanne) Medicine Background: Bilirubin has been identified as an endogenous antioxidant and cellular protectant. The present study was performed to clarify the potential influence of serum bilirubin on IgA vasculitis with nephritis (IgAV-N). Methods: One hundred and eighty-nine IgAV-N patients over 14 years old were enrolled. The patients were divided into two groups by the optimum cut-off value calculated by ROC curve. The composite endpoints were defined as a 60% decline in estimate glomerular filtration rate (e-GFR), end-stage renal disease (ESRD) and/or death. Kaplan-Meier (K-M) analysis and multivariate Cox analysis were carried out to determine the predictors for renal outcomes. In order to eliminate the influence of different baseline data, a 1:2 propensity score (PS) match was performed to make the results comparable and convictive. Results: The baseline data suggested that patients in low serum bilirubin group had significantly higher levels of systolic blood pressure, proteinuria, serum creatinine and crescent formation ratio and lower levels of serum albumin and hemoglobin. Renal survival analysis indicated that lower serum bilirubin levels were significantly correlated with a poorer prognosis. Multivariate Cox analysis demonstrated that the higher level of serum bilirubin was an independent protective factor for renal survival (HR, 0.172; 95% CI, 0.030–0.991; P = 0.049). After PS matching, the baseline characters of two groups had no statistical differences. Similar outcomes were demonstrated in K-M curve and the multivariate Cox analysis. Conclusion: Elevated bilirubin levels might be related to the favorable renal outcomes. Frontiers Media S.A. 2021-06-08 /pmc/articles/PMC8217633/ /pubmed/34169080 http://dx.doi.org/10.3389/fmed.2021.596151 Text en Copyright © 2021 Tan, Pei, Xu, Hu, Tan, Zhong, Tarun, Tang and Qin. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Medicine
Tan, Jiaxing
Pei, Gaiqin
Xu, Yicong
Hu, Tengyue
Tan, Li
Zhong, Zhengxia
Tarun, Padamata
Tang, Yi
Qin, Wei
Serum Bilirubin Is Correlated With the Progression of IgA Vasculitis With Nephritis
title Serum Bilirubin Is Correlated With the Progression of IgA Vasculitis With Nephritis
title_full Serum Bilirubin Is Correlated With the Progression of IgA Vasculitis With Nephritis
title_fullStr Serum Bilirubin Is Correlated With the Progression of IgA Vasculitis With Nephritis
title_full_unstemmed Serum Bilirubin Is Correlated With the Progression of IgA Vasculitis With Nephritis
title_short Serum Bilirubin Is Correlated With the Progression of IgA Vasculitis With Nephritis
title_sort serum bilirubin is correlated with the progression of iga vasculitis with nephritis
topic Medicine
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8217633/
https://www.ncbi.nlm.nih.gov/pubmed/34169080
http://dx.doi.org/10.3389/fmed.2021.596151
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