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Urine haptoglobin levels predict early renal functional decline in patients with type 2 diabetes
Diabetic nephropathy is the leading cause of end stage renal disease. The urinary albumin to creatinine ratio is used as a predictor for the development of nephropathy but it is neither sensitive nor specific. Here we used liquid chromatography/mass spectrometry on urine of eight normoalbuminuric pa...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2013
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3672380/ https://www.ncbi.nlm.nih.gov/pubmed/23536133 http://dx.doi.org/10.1038/ki.2013.57 |
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author | Bhensdadia, Nishant M. Hunt, Kelly J. Lopes-Virella, Maria F. Tucker, J. Michael Mataria, Mohammad R. Alge, Joseph L. Neely, Benjamin A Janech, Michael G. Arthur, John M. |
author_facet | Bhensdadia, Nishant M. Hunt, Kelly J. Lopes-Virella, Maria F. Tucker, J. Michael Mataria, Mohammad R. Alge, Joseph L. Neely, Benjamin A Janech, Michael G. Arthur, John M. |
author_sort | Bhensdadia, Nishant M. |
collection | PubMed |
description | Diabetic nephropathy is the leading cause of end stage renal disease. The urinary albumin to creatinine ratio is used as a predictor for the development of nephropathy but it is neither sensitive nor specific. Here we used liquid chromatography/mass spectrometry on urine of eight normoalbuminuric patients with type 2 diabetes from the VA Diabetes Trial to identify candidate markers for loss of renal function. Initial verification of 7 markers (agrin, haptoglobin, mannan-binding lectin serine protease 2, LAMP-2, angiotensinogen, NGAL and uromodulin) in the urine of an additional 30 patients showed that haptoglobin was the best predictor of early renal functional decline. We then measured this in the urine of 204 patients with type 2 diabetes who did not yet have significant kidney disease (eGFR stage 2 or better and an albumin to creatinine ratio less than 300 mg/g). In comparing the highest to lowest tertile, the odds ratio for having early renal function decline was 2.70 (CI 1.15, 6.32) using the haptoglobin to creatinine ratio compared to 2.50 (CI 1.14, 5.48) using the albumin to creatinine ratio after adjusting for treatment group and use of ACE inhibitors. Addition of the haptoglobin to creatinine ratio to a model using the albumin to creatinine ratio to predict early renal function decline resulted in improved predictive performance. Thus, the haptoglobin to creatinine ratio may be useful to predict patients with type 2 diabetes at risk of nephropathy prior to the development of macroalbuminuria or reduced GFR. |
format | Online Article Text |
id | pubmed-3672380 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
record_format | MEDLINE/PubMed |
spelling | pubmed-36723802013-12-01 Urine haptoglobin levels predict early renal functional decline in patients with type 2 diabetes Bhensdadia, Nishant M. Hunt, Kelly J. Lopes-Virella, Maria F. Tucker, J. Michael Mataria, Mohammad R. Alge, Joseph L. Neely, Benjamin A Janech, Michael G. Arthur, John M. Kidney Int Article Diabetic nephropathy is the leading cause of end stage renal disease. The urinary albumin to creatinine ratio is used as a predictor for the development of nephropathy but it is neither sensitive nor specific. Here we used liquid chromatography/mass spectrometry on urine of eight normoalbuminuric patients with type 2 diabetes from the VA Diabetes Trial to identify candidate markers for loss of renal function. Initial verification of 7 markers (agrin, haptoglobin, mannan-binding lectin serine protease 2, LAMP-2, angiotensinogen, NGAL and uromodulin) in the urine of an additional 30 patients showed that haptoglobin was the best predictor of early renal functional decline. We then measured this in the urine of 204 patients with type 2 diabetes who did not yet have significant kidney disease (eGFR stage 2 or better and an albumin to creatinine ratio less than 300 mg/g). In comparing the highest to lowest tertile, the odds ratio for having early renal function decline was 2.70 (CI 1.15, 6.32) using the haptoglobin to creatinine ratio compared to 2.50 (CI 1.14, 5.48) using the albumin to creatinine ratio after adjusting for treatment group and use of ACE inhibitors. Addition of the haptoglobin to creatinine ratio to a model using the albumin to creatinine ratio to predict early renal function decline resulted in improved predictive performance. Thus, the haptoglobin to creatinine ratio may be useful to predict patients with type 2 diabetes at risk of nephropathy prior to the development of macroalbuminuria or reduced GFR. 2013-03-27 2013-06 /pmc/articles/PMC3672380/ /pubmed/23536133 http://dx.doi.org/10.1038/ki.2013.57 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 Bhensdadia, Nishant M. Hunt, Kelly J. Lopes-Virella, Maria F. Tucker, J. Michael Mataria, Mohammad R. Alge, Joseph L. Neely, Benjamin A Janech, Michael G. Arthur, John M. Urine haptoglobin levels predict early renal functional decline in patients with type 2 diabetes |
title | Urine haptoglobin levels predict early renal functional decline in patients with type 2 diabetes |
title_full | Urine haptoglobin levels predict early renal functional decline in patients with type 2 diabetes |
title_fullStr | Urine haptoglobin levels predict early renal functional decline in patients with type 2 diabetes |
title_full_unstemmed | Urine haptoglobin levels predict early renal functional decline in patients with type 2 diabetes |
title_short | Urine haptoglobin levels predict early renal functional decline in patients with type 2 diabetes |
title_sort | urine haptoglobin levels predict early renal functional decline in patients with type 2 diabetes |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3672380/ https://www.ncbi.nlm.nih.gov/pubmed/23536133 http://dx.doi.org/10.1038/ki.2013.57 |
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