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Urinary Angiotensinogen as a Biomarker of Nephropathy in Childhood

While most circulating angiotensinogen (AGT) is synthesized in the liver, the kidneys also produce AGT. Recently, we reported that urinary AGT is mainly originated from AGT. Using newly developed human AGT ELISA, we measured urinary AGT levels in chronic glomerulonephritis (GN) patients and patients...

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Detalles Bibliográficos
Autores principales: Urushihara, Maki, Kagami, Shoji
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE-Hindawi Access to Research 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3153924/
https://www.ncbi.nlm.nih.gov/pubmed/21860793
http://dx.doi.org/10.4061/2011/206835
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author Urushihara, Maki
Kagami, Shoji
author_facet Urushihara, Maki
Kagami, Shoji
author_sort Urushihara, Maki
collection PubMed
description While most circulating angiotensinogen (AGT) is synthesized in the liver, the kidneys also produce AGT. Recently, we reported that urinary AGT is mainly originated from AGT. Using newly developed human AGT ELISA, we measured urinary AGT levels in chronic glomerulonephritis (GN) patients and patients with type 1 diabetes in childhood. Urinary AGT level was positively correlated with diastolic blood pressure, urinary albumin, urinary protein levels, and urinary occult blood in chronic GN patients. Furthermore, urinary AGT level was significantly increased in chronic GN patients not treated with renin-angiotensin system (RAS) blockers compared with control subjects. Importantly, patients treated with RAS blockers had a marked attenuation of this increase. Also, urinary AGT level was significantly higher in patients with diabetic nephropathy in the premicroalbuminuric phase than in control subjects. These results suggest that urinary AGT reflects intrarenal RAS status in chronic GN and may be an early marker of diabetic nephropathy.
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spelling pubmed-31539242011-08-22 Urinary Angiotensinogen as a Biomarker of Nephropathy in Childhood Urushihara, Maki Kagami, Shoji Int J Nephrol Review Article While most circulating angiotensinogen (AGT) is synthesized in the liver, the kidneys also produce AGT. Recently, we reported that urinary AGT is mainly originated from AGT. Using newly developed human AGT ELISA, we measured urinary AGT levels in chronic glomerulonephritis (GN) patients and patients with type 1 diabetes in childhood. Urinary AGT level was positively correlated with diastolic blood pressure, urinary albumin, urinary protein levels, and urinary occult blood in chronic GN patients. Furthermore, urinary AGT level was significantly increased in chronic GN patients not treated with renin-angiotensin system (RAS) blockers compared with control subjects. Importantly, patients treated with RAS blockers had a marked attenuation of this increase. Also, urinary AGT level was significantly higher in patients with diabetic nephropathy in the premicroalbuminuric phase than in control subjects. These results suggest that urinary AGT reflects intrarenal RAS status in chronic GN and may be an early marker of diabetic nephropathy. SAGE-Hindawi Access to Research 2011-08-09 /pmc/articles/PMC3153924/ /pubmed/21860793 http://dx.doi.org/10.4061/2011/206835 Text en Copyright © 2011 M. Urushihara and S. Kagami. 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 Review Article
Urushihara, Maki
Kagami, Shoji
Urinary Angiotensinogen as a Biomarker of Nephropathy in Childhood
title Urinary Angiotensinogen as a Biomarker of Nephropathy in Childhood
title_full Urinary Angiotensinogen as a Biomarker of Nephropathy in Childhood
title_fullStr Urinary Angiotensinogen as a Biomarker of Nephropathy in Childhood
title_full_unstemmed Urinary Angiotensinogen as a Biomarker of Nephropathy in Childhood
title_short Urinary Angiotensinogen as a Biomarker of Nephropathy in Childhood
title_sort urinary angiotensinogen as a biomarker of nephropathy in childhood
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3153924/
https://www.ncbi.nlm.nih.gov/pubmed/21860793
http://dx.doi.org/10.4061/2011/206835
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