TY - JOUR
T1 - N-Terminal Pro–B-Type Natriuretic Peptide and Incident CKD
AU - Sasaki, Takaya
AU - Oishi, Emi
AU - Nagata, Takuya
AU - Sakata, Satoko
AU - Chen, Sanmei
AU - Furuta, Yoshihiko
AU - Honda, Takanori
AU - Yoshida, Daigo
AU - Hata, Jun
AU - Tsuboi, Nobuo
AU - Kitazono, Takanari
AU - Yokoo, Takashi
AU - Ninomiya, Toshiharu
N1 - Funding Information:
Supported in part by Grants-in-Aid for Scientific Research A ( JP16H02692 ), B ( JP17H04126 , JP18H02737 , and JP19H03863 ), C ( JP18K07565 , JP18K09412 , JP19K07890 , JP20K10503 , and JP20K11020 ), Early-Career Scientists ( JP18K17925 ), and Research Activity Start-up ( JP19K23971 ) from the Ministry of Education, Culture, Sports, Science and Technology of Japan; by Health and Labour Sciences Research Grants of the Ministry of Health, Labour and Welfare of Japan ( 20FA1002 ); and by the Japan Agency for Medical Research and Development ( JP20dk0207025 , JP20km0405202 , and JP20fk0108075 ). We thank the staff of the Division of Health and Welfare of Hisayama for their cooperation in this study. The statistical analyses were performed using the computers offered under the category of General Projects by the Research Institute for Information Technology, Kyushu University.
Funding Information:
Supported in part by Grants-in-Aid for Scientific Research A (JP16H02692), B (JP17H04126, JP18H02737, and JP19H03863), C (JP18K07565, JP18K09412, JP19K07890, JP20K10503, and JP20K11020), Early-Career Scientists (JP18K17925), and Research Activity Start-up (JP19K23971) from the Ministry of Education, Culture, Sports, Science and Technology of Japan; by Health and Labour Sciences Research Grants of the Ministry of Health, Labour and Welfare of Japan (20FA1002); and by the Japan Agency for Medical Research and Development (JP20dk0207025, JP20km0405202, and JP20fk0108075). We thank the staff of the Division of Health and Welfare of Hisayama for their cooperation in this study. The statistical analyses were performed using the computers offered under the category of General Projects by the Research Institute for Information Technology, Kyushu University. Study concept and design: TS and TNi. Data collection: EO, SS, SC, YF, TH, DY, and JH. Data interpretation: TS, EO, TNa, SS, SC, YF, TH, DY, JH, and TNi. Statistical analysis: TS. Study coordination and performance: TNi. All authors contributed relevant intellectual content during manuscript drafting or revision and accepted accountability for the overall work by ensuring that questions on the accuracy or integrity of any portion of the work are appropriately investigated and resolved.
Publisher Copyright:
© 2021 International Society of Nephrology
PY - 2021/4
Y1 - 2021/4
N2 - 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/1.73m2 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.
AB - 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/1.73m2 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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U2 - 10.1016/j.ekir.2021.01.006
DO - 10.1016/j.ekir.2021.01.006
M3 - Article
AN - SCOPUS:85102085043
SN - 2468-0249
VL - 6
SP - 976
EP - 985
JO - Kidney International Reports
JF - Kidney International Reports
IS - 4
ER -