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Cystatin C, a marker for successful aging and glomerular filtration rate, is not influenced by inflammation

BACKGROUND: The plasma level of cystatin C is a better marker than plasma creatinine for successful aging. It has been assumed that the advantage of cystatin C is not only due to it being a better marker for glomerular filtration rate (GFR) than creatinine, but also because an inflammatory state of...

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Autores principales: Grubb, Anders, Björk, Jonas, Nyman, Ulf, Pollak, Joanna, Bengzon, Johan, Östner, Gustav, Lindström, Veronica
Formato: Texto
Lenguaje:English
Publicado: Informa Healthcare 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3072693/
https://www.ncbi.nlm.nih.gov/pubmed/21198422
http://dx.doi.org/10.3109/00365513.2010.546879
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author Grubb, Anders
Björk, Jonas
Nyman, Ulf
Pollak, Joanna
Bengzon, Johan
Östner, Gustav
Lindström, Veronica
author_facet Grubb, Anders
Björk, Jonas
Nyman, Ulf
Pollak, Joanna
Bengzon, Johan
Östner, Gustav
Lindström, Veronica
author_sort Grubb, Anders
collection PubMed
description BACKGROUND: The plasma level of cystatin C is a better marker than plasma creatinine for successful aging. It has been assumed that the advantage of cystatin C is not only due to it being a better marker for glomerular filtration rate (GFR) than creatinine, but also because an inflammatory state of a patient induces a raised cystatin C level. However, the observations of an association between cystatin C level and inflammation stem from large cohort studies. The present work concerns the cystatin C levels and degree of inflammation in longitudinal studies of individual subjects without infl ammation, who undergo elective surgery. METHODS: Cystatin C, creatinine, and the inflammatory markers CRP, serum amyloid A (SAA), haptoglobin and orosomucoid were measured in plasma samples from 35 patients the day before elective surgery and subsequently during seven consecutive days RESULTS: Twenty patients had CRP-levels below 1 mg/L before surgery and low levels of the additional inflammatory markers. Surgery caused marked inflammation with high peak values of CRP and SAA on the second day after the operation. The cystatin C level did not change significantly during the observation period and did not correlate significantly with the level of any of the four inflammatory markers. The creatinine level was significantly reduced on the first postoperative day but reached the preoperative level towards the end of the observation period. CONCLUSION: The inflammatory status of a patient does not influence the role of cystatin C as a marker of successful aging, nor of GFR.
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spelling pubmed-30726932011-04-12 Cystatin C, a marker for successful aging and glomerular filtration rate, is not influenced by inflammation Grubb, Anders Björk, Jonas Nyman, Ulf Pollak, Joanna Bengzon, Johan Östner, Gustav Lindström, Veronica Scand J Clin Lab Invest Original Article BACKGROUND: The plasma level of cystatin C is a better marker than plasma creatinine for successful aging. It has been assumed that the advantage of cystatin C is not only due to it being a better marker for glomerular filtration rate (GFR) than creatinine, but also because an inflammatory state of a patient induces a raised cystatin C level. However, the observations of an association between cystatin C level and inflammation stem from large cohort studies. The present work concerns the cystatin C levels and degree of inflammation in longitudinal studies of individual subjects without infl ammation, who undergo elective surgery. METHODS: Cystatin C, creatinine, and the inflammatory markers CRP, serum amyloid A (SAA), haptoglobin and orosomucoid were measured in plasma samples from 35 patients the day before elective surgery and subsequently during seven consecutive days RESULTS: Twenty patients had CRP-levels below 1 mg/L before surgery and low levels of the additional inflammatory markers. Surgery caused marked inflammation with high peak values of CRP and SAA on the second day after the operation. The cystatin C level did not change significantly during the observation period and did not correlate significantly with the level of any of the four inflammatory markers. The creatinine level was significantly reduced on the first postoperative day but reached the preoperative level towards the end of the observation period. CONCLUSION: The inflammatory status of a patient does not influence the role of cystatin C as a marker of successful aging, nor of GFR. Informa Healthcare 2011-04 2011-01-04 /pmc/articles/PMC3072693/ /pubmed/21198422 http://dx.doi.org/10.3109/00365513.2010.546879 Text en © 2011 Informa Healthcare http://creativecommons.org/licenses/by/2.0/ This is an open access article distributed under the Supplemental Terms and Conditions for iOpenAccess articles published in Informa Healthcare journals (http://www.informaworld.com/mpp/uploads/iopenaccess_tcs.pdf) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Grubb, Anders
Björk, Jonas
Nyman, Ulf
Pollak, Joanna
Bengzon, Johan
Östner, Gustav
Lindström, Veronica
Cystatin C, a marker for successful aging and glomerular filtration rate, is not influenced by inflammation
title Cystatin C, a marker for successful aging and glomerular filtration rate, is not influenced by inflammation
title_full Cystatin C, a marker for successful aging and glomerular filtration rate, is not influenced by inflammation
title_fullStr Cystatin C, a marker for successful aging and glomerular filtration rate, is not influenced by inflammation
title_full_unstemmed Cystatin C, a marker for successful aging and glomerular filtration rate, is not influenced by inflammation
title_short Cystatin C, a marker for successful aging and glomerular filtration rate, is not influenced by inflammation
title_sort cystatin c, a marker for successful aging and glomerular filtration rate, is not influenced by inflammation
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3072693/
https://www.ncbi.nlm.nih.gov/pubmed/21198422
http://dx.doi.org/10.3109/00365513.2010.546879
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