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Dividing CKD stage 3 into G3a and G3b could better predict the prognosis of IgA nephropathy

Chronic kidney disease (CKD) stage 3 was divided into stage G3a and stage G3b in the 2013 Kidney Disease Improving Global Outcomes guidelines. Whether it is appropriate to regard 45 mL/min/per 1.73 m(2) as the threshold value of G3a/G3b staging and whether dividing CKD stage 3 into G3a/G3b plays a u...

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Autores principales: Zhang, Jun-Jun, Yu, Gui-Zhen, Zheng, Zhao-Hui, Liu, Ya-Fei, Du, Yang-Yang, Quan, Song-Xia, Liu, Yu-Jie, Lv, Ji-Cheng, Zhang, Hong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5393865/
https://www.ncbi.nlm.nih.gov/pubmed/28414748
http://dx.doi.org/10.1371/journal.pone.0175828
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author Zhang, Jun-Jun
Yu, Gui-Zhen
Zheng, Zhao-Hui
Liu, Ya-Fei
Du, Yang-Yang
Quan, Song-Xia
Liu, Yu-Jie
Lv, Ji-Cheng
Zhang, Hong
author_facet Zhang, Jun-Jun
Yu, Gui-Zhen
Zheng, Zhao-Hui
Liu, Ya-Fei
Du, Yang-Yang
Quan, Song-Xia
Liu, Yu-Jie
Lv, Ji-Cheng
Zhang, Hong
author_sort Zhang, Jun-Jun
collection PubMed
description Chronic kidney disease (CKD) stage 3 was divided into stage G3a and stage G3b in the 2013 Kidney Disease Improving Global Outcomes guidelines. Whether it is appropriate to regard 45 mL/min/per 1.73 m(2) as the threshold value of G3a/G3b staging and whether dividing CKD stage 3 into G3a/G3b plays a useful role in assessing the prognosis of patients with IgA nephropathy (IgAN) remain unknown. Three hundred and ninety patients from the First Affiliated Hospital of Zhengzhou University and Peking University First Hospital diagnosed with IgAN in CKD stage 3 were enrolled and successfully followed up. Cox proportional hazards model was used to analyze hazard ratios of reaching the composite endpoints (doubling of serum creatinine, end-stage renal disease: estimated glomerular filtration rate (eGFR) <15 ml/min/per 1.73 m(2) or renal replacement therapy, or death) for patients with different eGFR and risk factors affecting composite endpoints. The Kaplan–Meier method was used to calculate the cumulative renal survival rate of patients. When eGFR was lower than 45 ml/min/per 1.73 m(2), the hazard ratio increased sharply for patients in CKD stage 3 who reached the composite endpoints. Renal injury and prognosis were significantly different between patients in the G3a and G3b groups. Stage G3b was a major risk factor affecting prognosis. A threshold value of 45 ml/min/per 1.73 m(2) appears appropriate to assess the prognosis of IgAN patients with CKD stage 3. Dividing IgAN patients with CKD stage 3 into G3a and G3b is very useful to help understand disease conditions and for predicting the risk for disease progression.
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spelling pubmed-53938652017-05-04 Dividing CKD stage 3 into G3a and G3b could better predict the prognosis of IgA nephropathy Zhang, Jun-Jun Yu, Gui-Zhen Zheng, Zhao-Hui Liu, Ya-Fei Du, Yang-Yang Quan, Song-Xia Liu, Yu-Jie Lv, Ji-Cheng Zhang, Hong PLoS One Research Article Chronic kidney disease (CKD) stage 3 was divided into stage G3a and stage G3b in the 2013 Kidney Disease Improving Global Outcomes guidelines. Whether it is appropriate to regard 45 mL/min/per 1.73 m(2) as the threshold value of G3a/G3b staging and whether dividing CKD stage 3 into G3a/G3b plays a useful role in assessing the prognosis of patients with IgA nephropathy (IgAN) remain unknown. Three hundred and ninety patients from the First Affiliated Hospital of Zhengzhou University and Peking University First Hospital diagnosed with IgAN in CKD stage 3 were enrolled and successfully followed up. Cox proportional hazards model was used to analyze hazard ratios of reaching the composite endpoints (doubling of serum creatinine, end-stage renal disease: estimated glomerular filtration rate (eGFR) <15 ml/min/per 1.73 m(2) or renal replacement therapy, or death) for patients with different eGFR and risk factors affecting composite endpoints. The Kaplan–Meier method was used to calculate the cumulative renal survival rate of patients. When eGFR was lower than 45 ml/min/per 1.73 m(2), the hazard ratio increased sharply for patients in CKD stage 3 who reached the composite endpoints. Renal injury and prognosis were significantly different between patients in the G3a and G3b groups. Stage G3b was a major risk factor affecting prognosis. A threshold value of 45 ml/min/per 1.73 m(2) appears appropriate to assess the prognosis of IgAN patients with CKD stage 3. Dividing IgAN patients with CKD stage 3 into G3a and G3b is very useful to help understand disease conditions and for predicting the risk for disease progression. Public Library of Science 2017-04-17 /pmc/articles/PMC5393865/ /pubmed/28414748 http://dx.doi.org/10.1371/journal.pone.0175828 Text en © 2017 Zhang 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
Zhang, Jun-Jun
Yu, Gui-Zhen
Zheng, Zhao-Hui
Liu, Ya-Fei
Du, Yang-Yang
Quan, Song-Xia
Liu, Yu-Jie
Lv, Ji-Cheng
Zhang, Hong
Dividing CKD stage 3 into G3a and G3b could better predict the prognosis of IgA nephropathy
title Dividing CKD stage 3 into G3a and G3b could better predict the prognosis of IgA nephropathy
title_full Dividing CKD stage 3 into G3a and G3b could better predict the prognosis of IgA nephropathy
title_fullStr Dividing CKD stage 3 into G3a and G3b could better predict the prognosis of IgA nephropathy
title_full_unstemmed Dividing CKD stage 3 into G3a and G3b could better predict the prognosis of IgA nephropathy
title_short Dividing CKD stage 3 into G3a and G3b could better predict the prognosis of IgA nephropathy
title_sort dividing ckd stage 3 into g3a and g3b could better predict the prognosis of iga nephropathy
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5393865/
https://www.ncbi.nlm.nih.gov/pubmed/28414748
http://dx.doi.org/10.1371/journal.pone.0175828
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