Circulating Fibroblast Growth Factor-23 Levels are Associated with an Increased Risk of Anemia Development in Patients with Nondialysis Chronic Kidney Disease

Abstract Fibroblast growth factor-23 (FGF23) is an established biomarker of adverse outcomes in patients with chronic kidney disease (CKD). Several cross-sectional studies have suggested a possible association between FGF23 and anemia in these patients. In this large-scale prospective cohort study,...

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Autores principales: Ki Heon Nam, Hyoungnae Kim, Seong Yeong An, Misol Lee, Min-Uk Cha, Jung Tak Park, Tae-Hyun Yoo, Kyu-Beck Lee, Yeong-Hoon Kim, Su-Ah Sung, Joongyub Lee, Shin-Wook Kang, Kyu Hun Choi, Curie Ahn, Seung Hyeok Han
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Publicado: Nature Portfolio 2018
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spelling oai:doaj.org-article:48611d3684df48dc901ec99d0869807d2021-12-02T16:08:25ZCirculating Fibroblast Growth Factor-23 Levels are Associated with an Increased Risk of Anemia Development in Patients with Nondialysis Chronic Kidney Disease10.1038/s41598-018-25439-z2045-2322https://doaj.org/article/48611d3684df48dc901ec99d0869807d2018-05-01T00:00:00Zhttps://doi.org/10.1038/s41598-018-25439-zhttps://doaj.org/toc/2045-2322Abstract Fibroblast growth factor-23 (FGF23) is an established biomarker of adverse outcomes in patients with chronic kidney disease (CKD). Several cross-sectional studies have suggested a possible association between FGF23 and anemia in these patients. In this large-scale prospective cohort study, we investigated this relationship and examined whether high FGF23 levels increase the risk of incident anemia. This prospective longitudinal study included 2,089 patients from the KoreaN cohort study for Outcome in patients With CKD. Anemia was defined as hemoglobin level <13.0 g/dl (men) and <12.0 g/dl (women). Log-transformed FGF23 significantly correlated with hepcidin but inversely correlated with iron profiles and hemoglobin. Multivariate logistic regression showed that log-transformed FGF23 was independently associated with anemia (odds ratio [OR], 1.14; 95% confidence interval [CI], 1.04–1.24, P = 0.01). Among 1,164 patients without anemia at baseline, 295 (25.3%) developed anemia during a median follow-up of 21 months. In fully adjusted multivariable Cox models, the risk of anemia development was significantly higher in the third (hazard ratio [HR], 1.66; 95% CI, 1.11–2.47; P = 0.01) and fourth (HR, 1.84; 95% CI, 1.23–2.76; P = 0.001) than in the first FGF23 quartile. In conclusion, high serum FGF23 levels were associated with an increased risk for anemia in patients with nondialysis CKD.Ki Heon NamHyoungnae KimSeong Yeong AnMisol LeeMin-Uk ChaJung Tak ParkTae-Hyun YooKyu-Beck LeeYeong-Hoon KimSu-Ah SungJoongyub LeeShin-Wook KangKyu Hun ChoiCurie AhnSeung Hyeok HanNature PortfolioarticleMedicineRScienceQENScientific Reports, Vol 8, Iss 1, Pp 1-10 (2018)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Ki Heon Nam
Hyoungnae Kim
Seong Yeong An
Misol Lee
Min-Uk Cha
Jung Tak Park
Tae-Hyun Yoo
Kyu-Beck Lee
Yeong-Hoon Kim
Su-Ah Sung
Joongyub Lee
Shin-Wook Kang
Kyu Hun Choi
Curie Ahn
Seung Hyeok Han
Circulating Fibroblast Growth Factor-23 Levels are Associated with an Increased Risk of Anemia Development in Patients with Nondialysis Chronic Kidney Disease
description Abstract Fibroblast growth factor-23 (FGF23) is an established biomarker of adverse outcomes in patients with chronic kidney disease (CKD). Several cross-sectional studies have suggested a possible association between FGF23 and anemia in these patients. In this large-scale prospective cohort study, we investigated this relationship and examined whether high FGF23 levels increase the risk of incident anemia. This prospective longitudinal study included 2,089 patients from the KoreaN cohort study for Outcome in patients With CKD. Anemia was defined as hemoglobin level <13.0 g/dl (men) and <12.0 g/dl (women). Log-transformed FGF23 significantly correlated with hepcidin but inversely correlated with iron profiles and hemoglobin. Multivariate logistic regression showed that log-transformed FGF23 was independently associated with anemia (odds ratio [OR], 1.14; 95% confidence interval [CI], 1.04–1.24, P = 0.01). Among 1,164 patients without anemia at baseline, 295 (25.3%) developed anemia during a median follow-up of 21 months. In fully adjusted multivariable Cox models, the risk of anemia development was significantly higher in the third (hazard ratio [HR], 1.66; 95% CI, 1.11–2.47; P = 0.01) and fourth (HR, 1.84; 95% CI, 1.23–2.76; P = 0.001) than in the first FGF23 quartile. In conclusion, high serum FGF23 levels were associated with an increased risk for anemia in patients with nondialysis CKD.
format article
author Ki Heon Nam
Hyoungnae Kim
Seong Yeong An
Misol Lee
Min-Uk Cha
Jung Tak Park
Tae-Hyun Yoo
Kyu-Beck Lee
Yeong-Hoon Kim
Su-Ah Sung
Joongyub Lee
Shin-Wook Kang
Kyu Hun Choi
Curie Ahn
Seung Hyeok Han
author_facet Ki Heon Nam
Hyoungnae Kim
Seong Yeong An
Misol Lee
Min-Uk Cha
Jung Tak Park
Tae-Hyun Yoo
Kyu-Beck Lee
Yeong-Hoon Kim
Su-Ah Sung
Joongyub Lee
Shin-Wook Kang
Kyu Hun Choi
Curie Ahn
Seung Hyeok Han
author_sort Ki Heon Nam
title Circulating Fibroblast Growth Factor-23 Levels are Associated with an Increased Risk of Anemia Development in Patients with Nondialysis Chronic Kidney Disease
title_short Circulating Fibroblast Growth Factor-23 Levels are Associated with an Increased Risk of Anemia Development in Patients with Nondialysis Chronic Kidney Disease
title_full Circulating Fibroblast Growth Factor-23 Levels are Associated with an Increased Risk of Anemia Development in Patients with Nondialysis Chronic Kidney Disease
title_fullStr Circulating Fibroblast Growth Factor-23 Levels are Associated with an Increased Risk of Anemia Development in Patients with Nondialysis Chronic Kidney Disease
title_full_unstemmed Circulating Fibroblast Growth Factor-23 Levels are Associated with an Increased Risk of Anemia Development in Patients with Nondialysis Chronic Kidney Disease
title_sort circulating fibroblast growth factor-23 levels are associated with an increased risk of anemia development in patients with nondialysis chronic kidney disease
publisher Nature Portfolio
publishDate 2018
url https://doaj.org/article/48611d3684df48dc901ec99d0869807d
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