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N-Terminal Pro–B-Type Natriuretic Peptide and Incident CKD

INTRODUCTION: Serum N-terminal pro–B-type natriuretic peptide (NT-proBNP) levels have been associated with the progression of kidney impairment among patients with chronic kidney disease (CKD), but only a few studies have investigated the association between serum NT-proBNP levels and incident CKD i...

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Autores principales: Sasaki, Takaya, Oishi, Emi, Nagata, Takuya, Sakata, Satoko, Chen, Sanmei, Furuta, Yoshihiko, Honda, Takanori, Yoshida, Daigo, Hata, Jun, Tsuboi, Nobuo, Kitazono, Takanari, Yokoo, Takashi, Ninomiya, Toshiharu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8071624/
https://www.ncbi.nlm.nih.gov/pubmed/33912747
http://dx.doi.org/10.1016/j.ekir.2021.01.006
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author Sasaki, Takaya
Oishi, Emi
Nagata, Takuya
Sakata, Satoko
Chen, Sanmei
Furuta, Yoshihiko
Honda, Takanori
Yoshida, Daigo
Hata, Jun
Tsuboi, Nobuo
Kitazono, Takanari
Yokoo, Takashi
Ninomiya, Toshiharu
author_facet Sasaki, Takaya
Oishi, Emi
Nagata, Takuya
Sakata, Satoko
Chen, Sanmei
Furuta, Yoshihiko
Honda, Takanori
Yoshida, Daigo
Hata, Jun
Tsuboi, Nobuo
Kitazono, Takanari
Yokoo, Takashi
Ninomiya, Toshiharu
author_sort Sasaki, Takaya
collection PubMed
description INTRODUCTION: Serum N-terminal pro–B-type natriuretic peptide (NT-proBNP) levels have been associated with the progression of kidney impairment among patients with chronic kidney disease (CKD), but only a few studies have investigated the association between serum NT-proBNP levels and incident CKD in general populations. METHODS: A total of 2486 Japanese community-dwelling residents ≥40 years of age without CKD at baseline were followed up by repeated annual health examinations for 10 years. Participants were divided into 4 groups according to serum NT-proBNP levels. CKD was defined as an estimated glomerular filtration rate (eGFR) <60 ml/min/1.73m(2) or the presence of proteinuria. Cox proportional hazards models were used to estimate hazard ratios (HRs) for risk of CKD. Linear mixed models were used to compare changes in eGFR. RESULTS: During the follow-up period, 800 participants developed CKD. The multivariable-adjusted HRs (95% confidence intervals [CIs]) for developing CKD were 1.00 (reference), 1.32 (1.11–1.57), 1.40 (1.10–1.78), and 1.94 (1.38–2.73) for serum NT-proBNP levels of <55, 55–124, 125–299, and ≥300 pg/ml, respectively (P for trend <0.001). The decline of eGFR during the follow-up was significantly more rapid among participants with higher serum NT-proBNP levels (P for trend <0.001). Adding serum NT-proBNP to the model composed of known risk factors for CKD improved the predictive ability for developing CKD. CONCLUSIONS: Higher serum NT-proBNP levels were associated with greater risks of developing CKD and greater decline in eGFR. Serum NT-proBNP could be a useful biomarker for assessing the future risk of CKD in a general Japanese population.
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spelling pubmed-80716242021-04-27 N-Terminal Pro–B-Type Natriuretic Peptide and Incident CKD Sasaki, Takaya Oishi, Emi Nagata, Takuya Sakata, Satoko Chen, Sanmei Furuta, Yoshihiko Honda, Takanori Yoshida, Daigo Hata, Jun Tsuboi, Nobuo Kitazono, Takanari Yokoo, Takashi Ninomiya, Toshiharu Kidney Int Rep Clinical Research INTRODUCTION: Serum N-terminal pro–B-type natriuretic peptide (NT-proBNP) levels have been associated with the progression of kidney impairment among patients with chronic kidney disease (CKD), but only a few studies have investigated the association between serum NT-proBNP levels and incident CKD in general populations. METHODS: A total of 2486 Japanese community-dwelling residents ≥40 years of age without CKD at baseline were followed up by repeated annual health examinations for 10 years. Participants were divided into 4 groups according to serum NT-proBNP levels. CKD was defined as an estimated glomerular filtration rate (eGFR) <60 ml/min/1.73m(2) or the presence of proteinuria. Cox proportional hazards models were used to estimate hazard ratios (HRs) for risk of CKD. Linear mixed models were used to compare changes in eGFR. RESULTS: During the follow-up period, 800 participants developed CKD. The multivariable-adjusted HRs (95% confidence intervals [CIs]) for developing CKD were 1.00 (reference), 1.32 (1.11–1.57), 1.40 (1.10–1.78), and 1.94 (1.38–2.73) for serum NT-proBNP levels of <55, 55–124, 125–299, and ≥300 pg/ml, respectively (P for trend <0.001). The decline of eGFR during the follow-up was significantly more rapid among participants with higher serum NT-proBNP levels (P for trend <0.001). Adding serum NT-proBNP to the model composed of known risk factors for CKD improved the predictive ability for developing CKD. CONCLUSIONS: Higher serum NT-proBNP levels were associated with greater risks of developing CKD and greater decline in eGFR. Serum NT-proBNP could be a useful biomarker for assessing the future risk of CKD in a general Japanese population. Elsevier 2021-01-16 /pmc/articles/PMC8071624/ /pubmed/33912747 http://dx.doi.org/10.1016/j.ekir.2021.01.006 Text en © 2021 International Society of Nephrology. Published by Elsevier Inc. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Clinical Research
Sasaki, Takaya
Oishi, Emi
Nagata, Takuya
Sakata, Satoko
Chen, Sanmei
Furuta, Yoshihiko
Honda, Takanori
Yoshida, Daigo
Hata, Jun
Tsuboi, Nobuo
Kitazono, Takanari
Yokoo, Takashi
Ninomiya, Toshiharu
N-Terminal Pro–B-Type Natriuretic Peptide and Incident CKD
title N-Terminal Pro–B-Type Natriuretic Peptide and Incident CKD
title_full N-Terminal Pro–B-Type Natriuretic Peptide and Incident CKD
title_fullStr N-Terminal Pro–B-Type Natriuretic Peptide and Incident CKD
title_full_unstemmed N-Terminal Pro–B-Type Natriuretic Peptide and Incident CKD
title_short N-Terminal Pro–B-Type Natriuretic Peptide and Incident CKD
title_sort n-terminal pro–b-type natriuretic peptide and incident ckd
topic Clinical Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8071624/
https://www.ncbi.nlm.nih.gov/pubmed/33912747
http://dx.doi.org/10.1016/j.ekir.2021.01.006
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