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Effects of Therapy on Urine Neutrophil Gelatinase-Associated Lipocalin in Nondiabetic Glomerular Diseases with Proteinuria
Urine neutrophil gelatinase-associated lipocalin (NGAL) is widely used as a biomarker for acute kidney injury. Cross-sectional studies have shown that NGAL may be elevated in glomerular diseases, but there is limited information on the value of NGAL in predicting treatment response or on the changes...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4976195/ https://www.ncbi.nlm.nih.gov/pubmed/27525120 http://dx.doi.org/10.1155/2016/4904502 |
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author | Sirisopha, Amnuay Vanavanan, Somlak Chittamma, Anchalee Phakdeekitcharoen, Bunyong Thakkinstian, Ammarin Lertrit, Amornpan Sathirapongsasuti, Nuankanya Kitiyakara, Chagriya |
author_facet | Sirisopha, Amnuay Vanavanan, Somlak Chittamma, Anchalee Phakdeekitcharoen, Bunyong Thakkinstian, Ammarin Lertrit, Amornpan Sathirapongsasuti, Nuankanya Kitiyakara, Chagriya |
author_sort | Sirisopha, Amnuay |
collection | PubMed |
description | Urine neutrophil gelatinase-associated lipocalin (NGAL) is widely used as a biomarker for acute kidney injury. Cross-sectional studies have shown that NGAL may be elevated in glomerular diseases, but there is limited information on the value of NGAL in predicting treatment response or on the changes of NGAL levels after therapy. We prospectively evaluated the effects of therapy on NGAL in nondiabetic glomerular diseases. Urine NGAL was collected at biopsy and follow-up at 12 months. At baseline, NGAL in glomerular disease patients (n = 43) correlated with proteinuria, but not with glomerular filtration rate (GFR). After therapy with renin-angiotensin blockers and/or immune modulating agents, change of NGAL correlated with change of proteinuria, but not with change of GFR. NGAL at baseline was not different between patients in complete remission (CR) at follow-up compared to those not in remission (NR). Compared to baseline, NGAL at follow-up decreased in CR (n = 10), but not in NR. Change of NGAL was greater in CR than NR. In conclusion, the change of urine NGAL correlated with the change of proteinuria. Baseline NGAL was not a predictor of complete remission. Future studies will be necessary to determine the role of NGAL as a predictor of long term outcome in proteinuric glomerular diseases. |
format | Online Article Text |
id | pubmed-4976195 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-49761952016-08-14 Effects of Therapy on Urine Neutrophil Gelatinase-Associated Lipocalin in Nondiabetic Glomerular Diseases with Proteinuria Sirisopha, Amnuay Vanavanan, Somlak Chittamma, Anchalee Phakdeekitcharoen, Bunyong Thakkinstian, Ammarin Lertrit, Amornpan Sathirapongsasuti, Nuankanya Kitiyakara, Chagriya Int J Nephrol Research Article Urine neutrophil gelatinase-associated lipocalin (NGAL) is widely used as a biomarker for acute kidney injury. Cross-sectional studies have shown that NGAL may be elevated in glomerular diseases, but there is limited information on the value of NGAL in predicting treatment response or on the changes of NGAL levels after therapy. We prospectively evaluated the effects of therapy on NGAL in nondiabetic glomerular diseases. Urine NGAL was collected at biopsy and follow-up at 12 months. At baseline, NGAL in glomerular disease patients (n = 43) correlated with proteinuria, but not with glomerular filtration rate (GFR). After therapy with renin-angiotensin blockers and/or immune modulating agents, change of NGAL correlated with change of proteinuria, but not with change of GFR. NGAL at baseline was not different between patients in complete remission (CR) at follow-up compared to those not in remission (NR). Compared to baseline, NGAL at follow-up decreased in CR (n = 10), but not in NR. Change of NGAL was greater in CR than NR. In conclusion, the change of urine NGAL correlated with the change of proteinuria. Baseline NGAL was not a predictor of complete remission. Future studies will be necessary to determine the role of NGAL as a predictor of long term outcome in proteinuric glomerular diseases. Hindawi Publishing Corporation 2016 2016-07-25 /pmc/articles/PMC4976195/ /pubmed/27525120 http://dx.doi.org/10.1155/2016/4904502 Text en Copyright © 2016 Amnuay Sirisopha et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Sirisopha, Amnuay Vanavanan, Somlak Chittamma, Anchalee Phakdeekitcharoen, Bunyong Thakkinstian, Ammarin Lertrit, Amornpan Sathirapongsasuti, Nuankanya Kitiyakara, Chagriya Effects of Therapy on Urine Neutrophil Gelatinase-Associated Lipocalin in Nondiabetic Glomerular Diseases with Proteinuria |
title | Effects of Therapy on Urine Neutrophil Gelatinase-Associated Lipocalin in Nondiabetic Glomerular Diseases with Proteinuria |
title_full | Effects of Therapy on Urine Neutrophil Gelatinase-Associated Lipocalin in Nondiabetic Glomerular Diseases with Proteinuria |
title_fullStr | Effects of Therapy on Urine Neutrophil Gelatinase-Associated Lipocalin in Nondiabetic Glomerular Diseases with Proteinuria |
title_full_unstemmed | Effects of Therapy on Urine Neutrophil Gelatinase-Associated Lipocalin in Nondiabetic Glomerular Diseases with Proteinuria |
title_short | Effects of Therapy on Urine Neutrophil Gelatinase-Associated Lipocalin in Nondiabetic Glomerular Diseases with Proteinuria |
title_sort | effects of therapy on urine neutrophil gelatinase-associated lipocalin in nondiabetic glomerular diseases with proteinuria |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4976195/ https://www.ncbi.nlm.nih.gov/pubmed/27525120 http://dx.doi.org/10.1155/2016/4904502 |
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