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The eGFR-C study: accuracy of glomerular filtration rate (GFR) estimation using creatinine and cystatin C and albuminuria for monitoring disease progression in patients with stage 3 chronic kidney disease - prospective longitudinal study in a multiethnic population

BACKGROUND: Uncertainty exists regarding the optimal method to estimate glomerular filtration rate (GFR) for disease detection and monitoring. Widely used GFR estimates have not been validated in British ethnic minority populations. METHODS/DESIGN: Iohexol measured GFR will be the reference against...

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Autores principales: Lamb, Edmund J, Brettell, Elizabeth A, Cockwell, Paul, Dalton, Neil, Deeks, Jon J, Harris, Kevin, Higgins, Tracy, Kalra, Philip A, Khunti, Kamlesh, Loud, Fiona, Ottridge, Ryan S, Sharpe, Claire C, Sitch, Alice J, Stevens, Paul E, Sutton, Andrew J, Taal, Maarten W
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3898236/
https://www.ncbi.nlm.nih.gov/pubmed/24423077
http://dx.doi.org/10.1186/1471-2369-15-13
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author Lamb, Edmund J
Brettell, Elizabeth A
Cockwell, Paul
Dalton, Neil
Deeks, Jon J
Harris, Kevin
Higgins, Tracy
Kalra, Philip A
Khunti, Kamlesh
Loud, Fiona
Ottridge, Ryan S
Sharpe, Claire C
Sitch, Alice J
Stevens, Paul E
Sutton, Andrew J
Taal, Maarten W
author_facet Lamb, Edmund J
Brettell, Elizabeth A
Cockwell, Paul
Dalton, Neil
Deeks, Jon J
Harris, Kevin
Higgins, Tracy
Kalra, Philip A
Khunti, Kamlesh
Loud, Fiona
Ottridge, Ryan S
Sharpe, Claire C
Sitch, Alice J
Stevens, Paul E
Sutton, Andrew J
Taal, Maarten W
author_sort Lamb, Edmund J
collection PubMed
description BACKGROUND: Uncertainty exists regarding the optimal method to estimate glomerular filtration rate (GFR) for disease detection and monitoring. Widely used GFR estimates have not been validated in British ethnic minority populations. METHODS/DESIGN: Iohexol measured GFR will be the reference against which each estimating equation will be compared. The estimating equations will be based upon serum creatinine and/or cystatin C. The eGFR-C study has 5 components: 1) A prospective longitudinal cohort study of 1300 adults with stage 3 chronic kidney disease followed for 3 years with reference (measured) GFR and test (estimated GFR [eGFR] and urinary albumin-to-creatinine ratio) measurements at baseline and 3 years. Test measurements will also be undertaken every 6 months. The study population will include a representative sample of South-Asians and African-Caribbeans. People with diabetes and proteinuria (ACR ≥30 mg/mmol) will comprise 20-30% of the study cohort. 2) A sub-study of patterns of disease progression of 375 people (125 each of Caucasian, Asian and African-Caribbean origin; in each case containing subjects at high and low risk of renal progression). Additional reference GFR measurements will be undertaken after 1 and 2 years to enable a model of disease progression and error to be built. 3) A biological variability study to establish reference change values for reference and test measures. 4) A modelling study of the performance of monitoring strategies on detecting progression, utilising estimates of accuracy, patterns of disease progression and estimates of measurement error from studies 1), 2) and 3). 5) A comprehensive cost database for each diagnostic approach will be developed to enable cost-effectiveness modelling of the optimal strategy. The performance of the estimating equations will be evaluated by assessing bias, precision and accuracy. Data will be modelled as a linear function of time utilising all available (maximum 7) time points compared with the difference between baseline and final reference values. The percentage of participants demonstrating large error with the respective estimating equations will be compared. Predictive value of GFR estimates and albumin-to-creatinine ratio will be compared amongst subjects that do or do not show progressive kidney function decline. DISCUSSION: The eGFR-C study will provide evidence to inform the optimal GFR estimate to be used in clinical practice. TRIAL REGISTRATION: ISRCTN42955626.
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spelling pubmed-38982362014-01-23 The eGFR-C study: accuracy of glomerular filtration rate (GFR) estimation using creatinine and cystatin C and albuminuria for monitoring disease progression in patients with stage 3 chronic kidney disease - prospective longitudinal study in a multiethnic population Lamb, Edmund J Brettell, Elizabeth A Cockwell, Paul Dalton, Neil Deeks, Jon J Harris, Kevin Higgins, Tracy Kalra, Philip A Khunti, Kamlesh Loud, Fiona Ottridge, Ryan S Sharpe, Claire C Sitch, Alice J Stevens, Paul E Sutton, Andrew J Taal, Maarten W BMC Nephrol Study Protocol BACKGROUND: Uncertainty exists regarding the optimal method to estimate glomerular filtration rate (GFR) for disease detection and monitoring. Widely used GFR estimates have not been validated in British ethnic minority populations. METHODS/DESIGN: Iohexol measured GFR will be the reference against which each estimating equation will be compared. The estimating equations will be based upon serum creatinine and/or cystatin C. The eGFR-C study has 5 components: 1) A prospective longitudinal cohort study of 1300 adults with stage 3 chronic kidney disease followed for 3 years with reference (measured) GFR and test (estimated GFR [eGFR] and urinary albumin-to-creatinine ratio) measurements at baseline and 3 years. Test measurements will also be undertaken every 6 months. The study population will include a representative sample of South-Asians and African-Caribbeans. People with diabetes and proteinuria (ACR ≥30 mg/mmol) will comprise 20-30% of the study cohort. 2) A sub-study of patterns of disease progression of 375 people (125 each of Caucasian, Asian and African-Caribbean origin; in each case containing subjects at high and low risk of renal progression). Additional reference GFR measurements will be undertaken after 1 and 2 years to enable a model of disease progression and error to be built. 3) A biological variability study to establish reference change values for reference and test measures. 4) A modelling study of the performance of monitoring strategies on detecting progression, utilising estimates of accuracy, patterns of disease progression and estimates of measurement error from studies 1), 2) and 3). 5) A comprehensive cost database for each diagnostic approach will be developed to enable cost-effectiveness modelling of the optimal strategy. The performance of the estimating equations will be evaluated by assessing bias, precision and accuracy. Data will be modelled as a linear function of time utilising all available (maximum 7) time points compared with the difference between baseline and final reference values. The percentage of participants demonstrating large error with the respective estimating equations will be compared. Predictive value of GFR estimates and albumin-to-creatinine ratio will be compared amongst subjects that do or do not show progressive kidney function decline. DISCUSSION: The eGFR-C study will provide evidence to inform the optimal GFR estimate to be used in clinical practice. TRIAL REGISTRATION: ISRCTN42955626. BioMed Central 2014-01-14 /pmc/articles/PMC3898236/ /pubmed/24423077 http://dx.doi.org/10.1186/1471-2369-15-13 Text en Copyright © 2014 Lamb et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Study Protocol
Lamb, Edmund J
Brettell, Elizabeth A
Cockwell, Paul
Dalton, Neil
Deeks, Jon J
Harris, Kevin
Higgins, Tracy
Kalra, Philip A
Khunti, Kamlesh
Loud, Fiona
Ottridge, Ryan S
Sharpe, Claire C
Sitch, Alice J
Stevens, Paul E
Sutton, Andrew J
Taal, Maarten W
The eGFR-C study: accuracy of glomerular filtration rate (GFR) estimation using creatinine and cystatin C and albuminuria for monitoring disease progression in patients with stage 3 chronic kidney disease - prospective longitudinal study in a multiethnic population
title The eGFR-C study: accuracy of glomerular filtration rate (GFR) estimation using creatinine and cystatin C and albuminuria for monitoring disease progression in patients with stage 3 chronic kidney disease - prospective longitudinal study in a multiethnic population
title_full The eGFR-C study: accuracy of glomerular filtration rate (GFR) estimation using creatinine and cystatin C and albuminuria for monitoring disease progression in patients with stage 3 chronic kidney disease - prospective longitudinal study in a multiethnic population
title_fullStr The eGFR-C study: accuracy of glomerular filtration rate (GFR) estimation using creatinine and cystatin C and albuminuria for monitoring disease progression in patients with stage 3 chronic kidney disease - prospective longitudinal study in a multiethnic population
title_full_unstemmed The eGFR-C study: accuracy of glomerular filtration rate (GFR) estimation using creatinine and cystatin C and albuminuria for monitoring disease progression in patients with stage 3 chronic kidney disease - prospective longitudinal study in a multiethnic population
title_short The eGFR-C study: accuracy of glomerular filtration rate (GFR) estimation using creatinine and cystatin C and albuminuria for monitoring disease progression in patients with stage 3 chronic kidney disease - prospective longitudinal study in a multiethnic population
title_sort egfr-c study: accuracy of glomerular filtration rate (gfr) estimation using creatinine and cystatin c and albuminuria for monitoring disease progression in patients with stage 3 chronic kidney disease - prospective longitudinal study in a multiethnic population
topic Study Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3898236/
https://www.ncbi.nlm.nih.gov/pubmed/24423077
http://dx.doi.org/10.1186/1471-2369-15-13
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