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Serum NGAL and FGF23 may have certain value in early diagnosis of CIN

Aims: This study aimed to assess whether neutrophil gelatinase-associated lipocalin (NGAL) and fibroblast growth factor 23 (FGF23) could be reliable biomarkers for early diagnosis of contrast-induced nephropathy (CIN). Methods: 202 patients who underwent percutaneous coronary intervention (PCI) were...

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Autores principales: Li, Huihui, Yu, Zaixin, Gan, Lu, Peng, Ling, Zhou, Qiaoling
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6171456/
https://www.ncbi.nlm.nih.gov/pubmed/30278796
http://dx.doi.org/10.1080/0886022X.2018.1487860
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author Li, Huihui
Yu, Zaixin
Gan, Lu
Peng, Ling
Zhou, Qiaoling
author_facet Li, Huihui
Yu, Zaixin
Gan, Lu
Peng, Ling
Zhou, Qiaoling
author_sort Li, Huihui
collection PubMed
description Aims: This study aimed to assess whether neutrophil gelatinase-associated lipocalin (NGAL) and fibroblast growth factor 23 (FGF23) could be reliable biomarkers for early diagnosis of contrast-induced nephropathy (CIN). Methods: 202 patients who underwent percutaneous coronary intervention (PCI) were included in the research. All subjects were divided into CIN group and non-CIN group. Serum NGAL and FGF23 were evaluated before and 0, 1, and 2 days after PCI. Serum levels of these two markers were compared intra-group and among groups. Receiver-operating characteristic (ROC) analysis and logistic regression models were conducted to assess the diagnostic performance of NGAL and FGF23 in detecting CIN. Results: When compared with baseline values, serum levels of both NGAL and FGF23 in all subjects increased after PCI, and the values peaked 1 day after PCI, but the changing was greater in CIN group. There were obvious differences between two groups in serum NGAL after 1, 2 days, and similar differences present in serum FGF23 after 1 day. ROC analysis showed that the area under the curve (AUC) of relative values (percent change from the baseline) in NGAL after 1 day was 0.899 (95% CI: 0.834–0.964, p = .000), the optimum cutoff was 49% (sensitivity = 80%, specificity = 92.4%). And the AUC in FGF23 was 0.814 (95% CI: 0.733–0.894, p = .000), the optimum cutoff was 20% (sensitivity = 73.3%, specificity = 87.6%). Both serum NGAL and serum FGF23 could improve the clinical models in identifying CIN. Conclusions: NGAL and FGF23 may have certain value in early diagnosis of CIN.
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spelling pubmed-61714562018-10-05 Serum NGAL and FGF23 may have certain value in early diagnosis of CIN Li, Huihui Yu, Zaixin Gan, Lu Peng, Ling Zhou, Qiaoling Ren Fail Clinical Study Aims: This study aimed to assess whether neutrophil gelatinase-associated lipocalin (NGAL) and fibroblast growth factor 23 (FGF23) could be reliable biomarkers for early diagnosis of contrast-induced nephropathy (CIN). Methods: 202 patients who underwent percutaneous coronary intervention (PCI) were included in the research. All subjects were divided into CIN group and non-CIN group. Serum NGAL and FGF23 were evaluated before and 0, 1, and 2 days after PCI. Serum levels of these two markers were compared intra-group and among groups. Receiver-operating characteristic (ROC) analysis and logistic regression models were conducted to assess the diagnostic performance of NGAL and FGF23 in detecting CIN. Results: When compared with baseline values, serum levels of both NGAL and FGF23 in all subjects increased after PCI, and the values peaked 1 day after PCI, but the changing was greater in CIN group. There were obvious differences between two groups in serum NGAL after 1, 2 days, and similar differences present in serum FGF23 after 1 day. ROC analysis showed that the area under the curve (AUC) of relative values (percent change from the baseline) in NGAL after 1 day was 0.899 (95% CI: 0.834–0.964, p = .000), the optimum cutoff was 49% (sensitivity = 80%, specificity = 92.4%). And the AUC in FGF23 was 0.814 (95% CI: 0.733–0.894, p = .000), the optimum cutoff was 20% (sensitivity = 73.3%, specificity = 87.6%). Both serum NGAL and serum FGF23 could improve the clinical models in identifying CIN. Conclusions: NGAL and FGF23 may have certain value in early diagnosis of CIN. Taylor & Francis 2018-10-03 /pmc/articles/PMC6171456/ /pubmed/30278796 http://dx.doi.org/10.1080/0886022X.2018.1487860 Text en © 2018 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. 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 work is properly cited.
spellingShingle Clinical Study
Li, Huihui
Yu, Zaixin
Gan, Lu
Peng, Ling
Zhou, Qiaoling
Serum NGAL and FGF23 may have certain value in early diagnosis of CIN
title Serum NGAL and FGF23 may have certain value in early diagnosis of CIN
title_full Serum NGAL and FGF23 may have certain value in early diagnosis of CIN
title_fullStr Serum NGAL and FGF23 may have certain value in early diagnosis of CIN
title_full_unstemmed Serum NGAL and FGF23 may have certain value in early diagnosis of CIN
title_short Serum NGAL and FGF23 may have certain value in early diagnosis of CIN
title_sort serum ngal and fgf23 may have certain value in early diagnosis of cin
topic Clinical Study
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6171456/
https://www.ncbi.nlm.nih.gov/pubmed/30278796
http://dx.doi.org/10.1080/0886022X.2018.1487860
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