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Improved equations estimating GFR in children with chronic kidney disease using an immunonephelometric determination of cystatin C
The Chronic Kidney Disease in Children study is a cohort of about 600 children with chronic kidney disease (CKD) in the United States and Canada. The independent variable for our observations was a measurement of glomerular filtration rate (GFR) by iohexol disappearance (iGFR) at the first two visit...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2012
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3433576/ https://www.ncbi.nlm.nih.gov/pubmed/22622496 http://dx.doi.org/10.1038/ki.2012.169 |
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author | Schwartz, George J. Schneider, Michael F. Maier, Paula S. Moxey-Mims, Marva Dharnidharka, Vikas R. Warady, Bradley Furth, Susan L. Muñoz, Alvaro |
author_facet | Schwartz, George J. Schneider, Michael F. Maier, Paula S. Moxey-Mims, Marva Dharnidharka, Vikas R. Warady, Bradley Furth, Susan L. Muñoz, Alvaro |
author_sort | Schwartz, George J. |
collection | PubMed |
description | The Chronic Kidney Disease in Children study is a cohort of about 600 children with chronic kidney disease (CKD) in the United States and Canada. The independent variable for our observations was a measurement of glomerular filtration rate (GFR) by iohexol disappearance (iGFR) at the first two visits one year apart and during alternate years thereafter. In a previous report, we had developed GFR estimating equations utilizing serum creatinine, blood urea nitrogen, height, gender and cystatin C measured by an immunoturbidimetric method; however the correlation coefficient of cystatin C and GFR (-0.69) was less robust than expected. Therefore, 495 samples were re-assayed using immunonephelometry. The reciprocal of immunonephelometric cystatin C was as well correlated with iGFR as was height/serum creatinine (both 0.88). We developed a new GFR estimating equation using a random 2/3 of 965 person-visits and applied it to the remaining 1/3 as a validation data set. In the validation data set, the correlation of the estimated GFR with iGFR was 0.92 with high precision and no bias; 91% and 45% of eGFR values were within 30% and 10% of iGFR, respectively. This equation works well in children with CKD in a range of GFR from 15 to 75 ml/min per 1.73 m(2). Further studies are needed to establish the applicability to children of normal stature and muscle mass, and higher GFR. |
format | Online Article Text |
id | pubmed-3433576 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
record_format | MEDLINE/PubMed |
spelling | pubmed-34335762013-02-01 Improved equations estimating GFR in children with chronic kidney disease using an immunonephelometric determination of cystatin C Schwartz, George J. Schneider, Michael F. Maier, Paula S. Moxey-Mims, Marva Dharnidharka, Vikas R. Warady, Bradley Furth, Susan L. Muñoz, Alvaro Kidney Int Article The Chronic Kidney Disease in Children study is a cohort of about 600 children with chronic kidney disease (CKD) in the United States and Canada. The independent variable for our observations was a measurement of glomerular filtration rate (GFR) by iohexol disappearance (iGFR) at the first two visits one year apart and during alternate years thereafter. In a previous report, we had developed GFR estimating equations utilizing serum creatinine, blood urea nitrogen, height, gender and cystatin C measured by an immunoturbidimetric method; however the correlation coefficient of cystatin C and GFR (-0.69) was less robust than expected. Therefore, 495 samples were re-assayed using immunonephelometry. The reciprocal of immunonephelometric cystatin C was as well correlated with iGFR as was height/serum creatinine (both 0.88). We developed a new GFR estimating equation using a random 2/3 of 965 person-visits and applied it to the remaining 1/3 as a validation data set. In the validation data set, the correlation of the estimated GFR with iGFR was 0.92 with high precision and no bias; 91% and 45% of eGFR values were within 30% and 10% of iGFR, respectively. This equation works well in children with CKD in a range of GFR from 15 to 75 ml/min per 1.73 m(2). Further studies are needed to establish the applicability to children of normal stature and muscle mass, and higher GFR. 2012-08 /pmc/articles/PMC3433576/ /pubmed/22622496 http://dx.doi.org/10.1038/ki.2012.169 Text en http://www.nature.com/authors/editorial_policies/license.html#terms Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use:http://www.nature.com/authors/editorial_policies/license.html#terms |
spellingShingle | Article Schwartz, George J. Schneider, Michael F. Maier, Paula S. Moxey-Mims, Marva Dharnidharka, Vikas R. Warady, Bradley Furth, Susan L. Muñoz, Alvaro Improved equations estimating GFR in children with chronic kidney disease using an immunonephelometric determination of cystatin C |
title | Improved equations estimating GFR in children with chronic kidney disease using an immunonephelometric determination of cystatin C |
title_full | Improved equations estimating GFR in children with chronic kidney disease using an immunonephelometric determination of cystatin C |
title_fullStr | Improved equations estimating GFR in children with chronic kidney disease using an immunonephelometric determination of cystatin C |
title_full_unstemmed | Improved equations estimating GFR in children with chronic kidney disease using an immunonephelometric determination of cystatin C |
title_short | Improved equations estimating GFR in children with chronic kidney disease using an immunonephelometric determination of cystatin C |
title_sort | improved equations estimating gfr in children with chronic kidney disease using an immunonephelometric determination of cystatin c |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3433576/ https://www.ncbi.nlm.nih.gov/pubmed/22622496 http://dx.doi.org/10.1038/ki.2012.169 |
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