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The evaluation of urinary calprotectin levels for prediction of acute cisplatin-induced nephrotoxicity

Calprotectin is a protein molecule that is released from inflammatory cells. Measurement of calprotectin in various body fluids has recently gained significant importance for differentiating inflammatory and noninflammatory events. The subject has aroused interest in the field of nephrology and some...

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Autores principales: Koçak, Gülay, Bilik, Gamze, Yeşilova, Aylia, Oyman, Firat, Can, Murat, Cihan, Şener
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9239626/
https://www.ncbi.nlm.nih.gov/pubmed/35777022
http://dx.doi.org/10.1097/MD.0000000000029814
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author Koçak, Gülay
Bilik, Gamze
Yeşilova, Aylia
Oyman, Firat
Can, Murat
Cihan, Şener
author_facet Koçak, Gülay
Bilik, Gamze
Yeşilova, Aylia
Oyman, Firat
Can, Murat
Cihan, Şener
author_sort Koçak, Gülay
collection PubMed
description Calprotectin is a protein molecule that is released from inflammatory cells. Measurement of calprotectin in various body fluids has recently gained significant importance for differentiating inflammatory and noninflammatory events. The subject has aroused interest in the field of nephrology and some renal pathologies in which urinary calprotectin levels have been studied. In this study, the measurement of urinary calprotectin level and its use for determining acute cisplatin nephrotoxicity in a group of patients with non-small cell lung cancer who received cisplatin-based oncological treatments have been investigated. The study included 41 patients who received cisplatin-based treatments for non-small cell lung cancer between January 2019 and January 2020. The patients were excluded from this study who were with estimated glomerular filtration rate (eGFR) <60 mL/min/1.73 m(2), serum creatinine (sCr) >1.5 mg/dL, a history of urinary tract infection, and nephrotoxic drug use in the past month. Baseline and 48-hour sCr values and baseline, 6-hour, 12-hour, 24-hour, and 48-hour urinary calprotectin levels of all patients were measured. Four of the 41 patients who received cisplatin treatment were excluded because their 48-hour sCr values could not be accessed. The control group included 29 patients. While there was no difference between the cisplatin group and the control group in terms of baseline sCr and eGFR values, the cisplatin group had significantly higher urinary calprotectin values. Of the 37 patients treated with cisplatin, 7 (18.9%) developed cisplatin-induced nephrotoxicity. The comparison of groups with (group 1) and without cisplatin nephrotoxicity (group 2) showed comparable mean age and male sex ratio. Baseline sCr and eGFR values were similar in both groups. The cisplatin-induced nephrotoxicity group had significantly higher 48-hour sCr and significantly lower 48-hour eGFR values. Baseline, 12-hour, 24-hour, and 48-hour urinary calprotectin levels were similar in groups with and without cisplatin nephrotoxicity. Recent studies have demonstrated that urinary calprotectin level measurement can be used to distinguish intrinsic acute kidney disease from prerenal kidney disease. However, the comparison of groups with and without cisplatin nephrotoxicity in our study showed no difference in urinary calprotectin levels. However, there is a need for large-scale studies using combined urinary biomarkers.
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spelling pubmed-92396262022-06-30 The evaluation of urinary calprotectin levels for prediction of acute cisplatin-induced nephrotoxicity Koçak, Gülay Bilik, Gamze Yeşilova, Aylia Oyman, Firat Can, Murat Cihan, Şener Medicine (Baltimore) Research Article Calprotectin is a protein molecule that is released from inflammatory cells. Measurement of calprotectin in various body fluids has recently gained significant importance for differentiating inflammatory and noninflammatory events. The subject has aroused interest in the field of nephrology and some renal pathologies in which urinary calprotectin levels have been studied. In this study, the measurement of urinary calprotectin level and its use for determining acute cisplatin nephrotoxicity in a group of patients with non-small cell lung cancer who received cisplatin-based oncological treatments have been investigated. The study included 41 patients who received cisplatin-based treatments for non-small cell lung cancer between January 2019 and January 2020. The patients were excluded from this study who were with estimated glomerular filtration rate (eGFR) <60 mL/min/1.73 m(2), serum creatinine (sCr) >1.5 mg/dL, a history of urinary tract infection, and nephrotoxic drug use in the past month. Baseline and 48-hour sCr values and baseline, 6-hour, 12-hour, 24-hour, and 48-hour urinary calprotectin levels of all patients were measured. Four of the 41 patients who received cisplatin treatment were excluded because their 48-hour sCr values could not be accessed. The control group included 29 patients. While there was no difference between the cisplatin group and the control group in terms of baseline sCr and eGFR values, the cisplatin group had significantly higher urinary calprotectin values. Of the 37 patients treated with cisplatin, 7 (18.9%) developed cisplatin-induced nephrotoxicity. The comparison of groups with (group 1) and without cisplatin nephrotoxicity (group 2) showed comparable mean age and male sex ratio. Baseline sCr and eGFR values were similar in both groups. The cisplatin-induced nephrotoxicity group had significantly higher 48-hour sCr and significantly lower 48-hour eGFR values. Baseline, 12-hour, 24-hour, and 48-hour urinary calprotectin levels were similar in groups with and without cisplatin nephrotoxicity. Recent studies have demonstrated that urinary calprotectin level measurement can be used to distinguish intrinsic acute kidney disease from prerenal kidney disease. However, the comparison of groups with and without cisplatin nephrotoxicity in our study showed no difference in urinary calprotectin levels. However, there is a need for large-scale studies using combined urinary biomarkers. Lippincott Williams & Wilkins 2022-06-30 /pmc/articles/PMC9239626/ /pubmed/35777022 http://dx.doi.org/10.1097/MD.0000000000029814 Text en Copyright © 2022 the Author(s). Published by Wolters Kluwer Health, Inc. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the Creative Commons Attribution License 4.0 (CCBY) (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Koçak, Gülay
Bilik, Gamze
Yeşilova, Aylia
Oyman, Firat
Can, Murat
Cihan, Şener
The evaluation of urinary calprotectin levels for prediction of acute cisplatin-induced nephrotoxicity
title The evaluation of urinary calprotectin levels for prediction of acute cisplatin-induced nephrotoxicity
title_full The evaluation of urinary calprotectin levels for prediction of acute cisplatin-induced nephrotoxicity
title_fullStr The evaluation of urinary calprotectin levels for prediction of acute cisplatin-induced nephrotoxicity
title_full_unstemmed The evaluation of urinary calprotectin levels for prediction of acute cisplatin-induced nephrotoxicity
title_short The evaluation of urinary calprotectin levels for prediction of acute cisplatin-induced nephrotoxicity
title_sort evaluation of urinary calprotectin levels for prediction of acute cisplatin-induced nephrotoxicity
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9239626/
https://www.ncbi.nlm.nih.gov/pubmed/35777022
http://dx.doi.org/10.1097/MD.0000000000029814
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