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Association of hsCRP, White Blood Cell Count and Ferritin with Renal Outcome in Chronic Kidney Disease Patients

Inflammation is a pathogenic factor in renal injury, but whether inflammation is related to renal outcome in chronic kidney disease (CKD) patients is little known. We thus assess the association of inflammation and renal outcome in an advanced CKD cohort. This study analyzed the association between...

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Autores principales: Tsai, Yi-Chun, Hung, Chi-Chih, Kuo, Mei-Chuan, Tsai, Jer-Chia, Yeh, Shih-Meng, Hwang, Shang-Jyh, Chiu, Yi-Wen, Kuo, Hung-Tien, Chang, Jer-Ming, Chen, Hung-Chun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3534111/
https://www.ncbi.nlm.nih.gov/pubmed/23300770
http://dx.doi.org/10.1371/journal.pone.0052775
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author Tsai, Yi-Chun
Hung, Chi-Chih
Kuo, Mei-Chuan
Tsai, Jer-Chia
Yeh, Shih-Meng
Hwang, Shang-Jyh
Chiu, Yi-Wen
Kuo, Hung-Tien
Chang, Jer-Ming
Chen, Hung-Chun
author_facet Tsai, Yi-Chun
Hung, Chi-Chih
Kuo, Mei-Chuan
Tsai, Jer-Chia
Yeh, Shih-Meng
Hwang, Shang-Jyh
Chiu, Yi-Wen
Kuo, Hung-Tien
Chang, Jer-Ming
Chen, Hung-Chun
author_sort Tsai, Yi-Chun
collection PubMed
description Inflammation is a pathogenic factor in renal injury, but whether inflammation is related to renal outcome in chronic kidney disease (CKD) patients is little known. We thus assess the association of inflammation and renal outcome in an advanced CKD cohort. This study analyzed the association between inflammatory markers, such as C-reactive protein (hsCRP), white blood cell (WBC) count and ferritin, renal replacement therapy (RRT) and rapid renal progression (estimated GFR slope<-6 ml/min/1.73 m(2)/y) in 3303 patients with stage 3–5 CKD. In all subjects, the mean hsCRP, WBC count, and ferritin levels were 1.2 (0.4, 5.4) mg/L, 7.2±2.3×10(3) cells/µL, and 200 (107,349) ng/mL, respectively. During a mean 3.2-year follow-up, there were 1080 (32.7%) subjects commencing RRT, and 841(25.5%) subjects presenting rapid renal progression. Both hsCRP and ferritin were associated with increased risk for RRT with the adjusted HR (tertile 3 versus tertile 1∶1.17 〔1.01–1.36〕 and 1.20 〔1.03–1.40〕, respectively). Both hsCRP and ferritin were associated with increased odds for rapid renal progression with the adjusted OR (tertile 3 versus tertile 1∶1.40 〔1.13–1.77〕 and 1.32 〔1.06–1.67〕, respectively). hsCRP and ferritin stratified by albumin were also associated with RRT and rapid renal progression. Instead, WBC count was not associated with renal outcome. In conclusion, elevated levels of hsCRP and ferritin are risk factors associated with RRT and rapid renal progression in advanced CKD patients.
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spelling pubmed-35341112013-01-08 Association of hsCRP, White Blood Cell Count and Ferritin with Renal Outcome in Chronic Kidney Disease Patients Tsai, Yi-Chun Hung, Chi-Chih Kuo, Mei-Chuan Tsai, Jer-Chia Yeh, Shih-Meng Hwang, Shang-Jyh Chiu, Yi-Wen Kuo, Hung-Tien Chang, Jer-Ming Chen, Hung-Chun PLoS One Research Article Inflammation is a pathogenic factor in renal injury, but whether inflammation is related to renal outcome in chronic kidney disease (CKD) patients is little known. We thus assess the association of inflammation and renal outcome in an advanced CKD cohort. This study analyzed the association between inflammatory markers, such as C-reactive protein (hsCRP), white blood cell (WBC) count and ferritin, renal replacement therapy (RRT) and rapid renal progression (estimated GFR slope<-6 ml/min/1.73 m(2)/y) in 3303 patients with stage 3–5 CKD. In all subjects, the mean hsCRP, WBC count, and ferritin levels were 1.2 (0.4, 5.4) mg/L, 7.2±2.3×10(3) cells/µL, and 200 (107,349) ng/mL, respectively. During a mean 3.2-year follow-up, there were 1080 (32.7%) subjects commencing RRT, and 841(25.5%) subjects presenting rapid renal progression. Both hsCRP and ferritin were associated with increased risk for RRT with the adjusted HR (tertile 3 versus tertile 1∶1.17 〔1.01–1.36〕 and 1.20 〔1.03–1.40〕, respectively). Both hsCRP and ferritin were associated with increased odds for rapid renal progression with the adjusted OR (tertile 3 versus tertile 1∶1.40 〔1.13–1.77〕 and 1.32 〔1.06–1.67〕, respectively). hsCRP and ferritin stratified by albumin were also associated with RRT and rapid renal progression. Instead, WBC count was not associated with renal outcome. In conclusion, elevated levels of hsCRP and ferritin are risk factors associated with RRT and rapid renal progression in advanced CKD patients. Public Library of Science 2012-12-31 /pmc/articles/PMC3534111/ /pubmed/23300770 http://dx.doi.org/10.1371/journal.pone.0052775 Text en © 2012 Tsai 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, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Tsai, Yi-Chun
Hung, Chi-Chih
Kuo, Mei-Chuan
Tsai, Jer-Chia
Yeh, Shih-Meng
Hwang, Shang-Jyh
Chiu, Yi-Wen
Kuo, Hung-Tien
Chang, Jer-Ming
Chen, Hung-Chun
Association of hsCRP, White Blood Cell Count and Ferritin with Renal Outcome in Chronic Kidney Disease Patients
title Association of hsCRP, White Blood Cell Count and Ferritin with Renal Outcome in Chronic Kidney Disease Patients
title_full Association of hsCRP, White Blood Cell Count and Ferritin with Renal Outcome in Chronic Kidney Disease Patients
title_fullStr Association of hsCRP, White Blood Cell Count and Ferritin with Renal Outcome in Chronic Kidney Disease Patients
title_full_unstemmed Association of hsCRP, White Blood Cell Count and Ferritin with Renal Outcome in Chronic Kidney Disease Patients
title_short Association of hsCRP, White Blood Cell Count and Ferritin with Renal Outcome in Chronic Kidney Disease Patients
title_sort association of hscrp, white blood cell count and ferritin with renal outcome in chronic kidney disease patients
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3534111/
https://www.ncbi.nlm.nih.gov/pubmed/23300770
http://dx.doi.org/10.1371/journal.pone.0052775
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