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Serum cystatin C can be used as a marker of renal function even in patients with intestinal urinary diversion
OBJECTIVE: Recently, serum cystatin C (CysC) has been used as a novel marker of renal function. However, there is a lack of data on CysC levels in patients with intestinal urinary diversion (UD). Here we report CysC levels in such patients. METHODS: We prospectively observed 38 patients who were dia...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Second Military Medical University
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5730715/ https://www.ncbi.nlm.nih.gov/pubmed/29264138 http://dx.doi.org/10.1016/j.ajur.2015.07.003 |
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author | Matsuki, Masahiro Tanaka, Toshiaki Maehana, Takeshi Ichihara, Koji Yanase, Masahiro Matsukawa, Masanori Adachi, Hideki Takahashi, Satoshi Masumori, Naoya |
author_facet | Matsuki, Masahiro Tanaka, Toshiaki Maehana, Takeshi Ichihara, Koji Yanase, Masahiro Matsukawa, Masanori Adachi, Hideki Takahashi, Satoshi Masumori, Naoya |
author_sort | Matsuki, Masahiro |
collection | PubMed |
description | OBJECTIVE: Recently, serum cystatin C (CysC) has been used as a novel marker of renal function. However, there is a lack of data on CysC levels in patients with intestinal urinary diversion (UD). Here we report CysC levels in such patients. METHODS: We prospectively observed 38 patients who were diagnosed with bladder cancer and subsequently treated with radical cystectomy and UD at our institution in 2012 and 2013. Serum creatinine (sCr) and CysC were obtained optionally at the same time at least 1 month after radical cystectomy and UD. RESULTS: The median CysC and sCr concentrations were 1.12 mg/L (range 0.75–2.47 mg/L) and 0.99 mg/dL (range 0.61–2.22 mg/dL), respectively. The median estimated concentrations of glomerular filtration rate (GFR) based on CysC (eGFRcys) and GFR based on creatinine (eGFRcreat) were 61.08 mL/min/1.73 m(2) (range 22.64–99.89 mL/min/1.73 m(2)) and 58.01 mL/min/1.73 m(2) (range 23.48–91.82 mL/min/1.73 m(2)), respectively. CysC had a significant correlation with sCr (r = 0.8607, p < 0.0001) and eGFRcreat (r = −0.8993, p < 0.0001). eGFRcys also had a significant correlation with eGFRcreat (r = 0.8104, p < 0.0001). CONCLUSION: The correlation between CysC and sCr was strong and the correlation coefficient was equivalent to that in patients without UD. The results suggest that CysC is not affected by UD and can be used as a marker of renal function similarly to sCr in patients with UD. |
format | Online Article Text |
id | pubmed-5730715 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Second Military Medical University |
record_format | MEDLINE/PubMed |
spelling | pubmed-57307152017-12-20 Serum cystatin C can be used as a marker of renal function even in patients with intestinal urinary diversion Matsuki, Masahiro Tanaka, Toshiaki Maehana, Takeshi Ichihara, Koji Yanase, Masahiro Matsukawa, Masanori Adachi, Hideki Takahashi, Satoshi Masumori, Naoya Asian J Urol Article OBJECTIVE: Recently, serum cystatin C (CysC) has been used as a novel marker of renal function. However, there is a lack of data on CysC levels in patients with intestinal urinary diversion (UD). Here we report CysC levels in such patients. METHODS: We prospectively observed 38 patients who were diagnosed with bladder cancer and subsequently treated with radical cystectomy and UD at our institution in 2012 and 2013. Serum creatinine (sCr) and CysC were obtained optionally at the same time at least 1 month after radical cystectomy and UD. RESULTS: The median CysC and sCr concentrations were 1.12 mg/L (range 0.75–2.47 mg/L) and 0.99 mg/dL (range 0.61–2.22 mg/dL), respectively. The median estimated concentrations of glomerular filtration rate (GFR) based on CysC (eGFRcys) and GFR based on creatinine (eGFRcreat) were 61.08 mL/min/1.73 m(2) (range 22.64–99.89 mL/min/1.73 m(2)) and 58.01 mL/min/1.73 m(2) (range 23.48–91.82 mL/min/1.73 m(2)), respectively. CysC had a significant correlation with sCr (r = 0.8607, p < 0.0001) and eGFRcreat (r = −0.8993, p < 0.0001). eGFRcys also had a significant correlation with eGFRcreat (r = 0.8104, p < 0.0001). CONCLUSION: The correlation between CysC and sCr was strong and the correlation coefficient was equivalent to that in patients without UD. The results suggest that CysC is not affected by UD and can be used as a marker of renal function similarly to sCr in patients with UD. Second Military Medical University 2015-07 2015-07-15 /pmc/articles/PMC5730715/ /pubmed/29264138 http://dx.doi.org/10.1016/j.ajur.2015.07.003 Text en © 2015 Editorial Office of Asian Journal of Urology. Production and hosting by Elsevier (Singapore) Pte Ltd. http://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 | Article Matsuki, Masahiro Tanaka, Toshiaki Maehana, Takeshi Ichihara, Koji Yanase, Masahiro Matsukawa, Masanori Adachi, Hideki Takahashi, Satoshi Masumori, Naoya Serum cystatin C can be used as a marker of renal function even in patients with intestinal urinary diversion |
title | Serum cystatin C can be used as a marker of renal function even in patients with intestinal urinary diversion |
title_full | Serum cystatin C can be used as a marker of renal function even in patients with intestinal urinary diversion |
title_fullStr | Serum cystatin C can be used as a marker of renal function even in patients with intestinal urinary diversion |
title_full_unstemmed | Serum cystatin C can be used as a marker of renal function even in patients with intestinal urinary diversion |
title_short | Serum cystatin C can be used as a marker of renal function even in patients with intestinal urinary diversion |
title_sort | serum cystatin c can be used as a marker of renal function even in patients with intestinal urinary diversion |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5730715/ https://www.ncbi.nlm.nih.gov/pubmed/29264138 http://dx.doi.org/10.1016/j.ajur.2015.07.003 |
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