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Urinary Alpha- and Pi-Glutathione S-Transferases in Adult Patients with Type 1 Diabetes

BACKGROUND/AIMS: Glutathione S-transferases (GSTs) are cytosolic enzymes excreted from renal tubules following tubular damage. α-GST primarily originates from proximal tubules, while π-GST from distal tubules and collecting ducts. We investigated if GST levels are associated with renal function in p...

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Autores principales: von Scholten, Bernt Johan, Theilade, Simone, Lajer, Maria, Rossing, Peter
Formato: Online Artículo Texto
Lenguaje:English
Publicado: S. Karger AG 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4164068/
https://www.ncbi.nlm.nih.gov/pubmed/25337081
http://dx.doi.org/10.1159/000365481
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author von Scholten, Bernt Johan
Theilade, Simone
Lajer, Maria
Rossing, Peter
author_facet von Scholten, Bernt Johan
Theilade, Simone
Lajer, Maria
Rossing, Peter
author_sort von Scholten, Bernt Johan
collection PubMed
description BACKGROUND/AIMS: Glutathione S-transferases (GSTs) are cytosolic enzymes excreted from renal tubules following tubular damage. α-GST primarily originates from proximal tubules, while π-GST from distal tubules and collecting ducts. We investigated if GST levels are associated with renal function in patients with type 1 diabetes. METHODS: We conducted a cross-sectional study including 189 Caucasian patients with type 1 diabetes and 16 nondiabetic controls. α- and π-GST were measured by ELISA and reported as GST/urinary creatinine excretion (μg/mmol). RESULTS: The subjects were 53 ± 14 years old, 66 (35%) were female and the estimated glomerular filtration rate was 85 ± 29 ml/min/1.73 m(2). Normo- (<30 mg/24 h), micro- (30-299 mg/24 h) and macroalbuminuria (≥300 mg/24 h) was present in 57, 61 and 71 patients, respectively. α- and π-GST/creatinine ratios in controls versus all patients were 0.07 (0-0.3) and 0.11 (0-0.8) μg/mmol versus 0.05 (0-2.3) and 0.16 (0-4.9) μg/mmol (p ≥ 0.16; adjusted for age and gender, p ≥ 0.18). The α-GST/creatinine ratio positively correlated with female gender (p = 0.04), while the π-GST/creatinine ratio was associated with age and female gender (p ≤ 0.016). Comparing normo-, micro- and macroalbuminuric patients, α- and π-GST levels were similar (p = 0.10; adjusted p = 0.11). Neither α- nor π-GST levels were significantly associated with renal function (p ≥ 0.34). CONCLUSION: α- and π-GST/creatinine ratios were similar among controls and patients with type 1 diabetes. In addition, we did not find associations with albuminuria degree or level of renal function. The significance of increased or decreased excretion of α- and π-GST among patients with diabetes needs to be clarified.
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spelling pubmed-41640682014-10-21 Urinary Alpha- and Pi-Glutathione S-Transferases in Adult Patients with Type 1 Diabetes von Scholten, Bernt Johan Theilade, Simone Lajer, Maria Rossing, Peter Nephron Extra Original Paper BACKGROUND/AIMS: Glutathione S-transferases (GSTs) are cytosolic enzymes excreted from renal tubules following tubular damage. α-GST primarily originates from proximal tubules, while π-GST from distal tubules and collecting ducts. We investigated if GST levels are associated with renal function in patients with type 1 diabetes. METHODS: We conducted a cross-sectional study including 189 Caucasian patients with type 1 diabetes and 16 nondiabetic controls. α- and π-GST were measured by ELISA and reported as GST/urinary creatinine excretion (μg/mmol). RESULTS: The subjects were 53 ± 14 years old, 66 (35%) were female and the estimated glomerular filtration rate was 85 ± 29 ml/min/1.73 m(2). Normo- (<30 mg/24 h), micro- (30-299 mg/24 h) and macroalbuminuria (≥300 mg/24 h) was present in 57, 61 and 71 patients, respectively. α- and π-GST/creatinine ratios in controls versus all patients were 0.07 (0-0.3) and 0.11 (0-0.8) μg/mmol versus 0.05 (0-2.3) and 0.16 (0-4.9) μg/mmol (p ≥ 0.16; adjusted for age and gender, p ≥ 0.18). The α-GST/creatinine ratio positively correlated with female gender (p = 0.04), while the π-GST/creatinine ratio was associated with age and female gender (p ≤ 0.016). Comparing normo-, micro- and macroalbuminuric patients, α- and π-GST levels were similar (p = 0.10; adjusted p = 0.11). Neither α- nor π-GST levels were significantly associated with renal function (p ≥ 0.34). CONCLUSION: α- and π-GST/creatinine ratios were similar among controls and patients with type 1 diabetes. In addition, we did not find associations with albuminuria degree or level of renal function. The significance of increased or decreased excretion of α- and π-GST among patients with diabetes needs to be clarified. S. Karger AG 2014-07-31 /pmc/articles/PMC4164068/ /pubmed/25337081 http://dx.doi.org/10.1159/000365481 Text en Copyright © 2014 by S. Karger AG, Basel http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article licensed under the terms of the Creative Commons Attribution-NonCommercial 3.0 Unported license (CC BY-NC) (www.karger.com/OA-license), applicable to the online version of the article only. Users may download, print and share this work on the Internet for noncommercial purposes only, provided the original work is properly cited, and a link to the original work on http://www.karger.com and the terms of this license are included in any shared versions.
spellingShingle Original Paper
von Scholten, Bernt Johan
Theilade, Simone
Lajer, Maria
Rossing, Peter
Urinary Alpha- and Pi-Glutathione S-Transferases in Adult Patients with Type 1 Diabetes
title Urinary Alpha- and Pi-Glutathione S-Transferases in Adult Patients with Type 1 Diabetes
title_full Urinary Alpha- and Pi-Glutathione S-Transferases in Adult Patients with Type 1 Diabetes
title_fullStr Urinary Alpha- and Pi-Glutathione S-Transferases in Adult Patients with Type 1 Diabetes
title_full_unstemmed Urinary Alpha- and Pi-Glutathione S-Transferases in Adult Patients with Type 1 Diabetes
title_short Urinary Alpha- and Pi-Glutathione S-Transferases in Adult Patients with Type 1 Diabetes
title_sort urinary alpha- and pi-glutathione s-transferases in adult patients with type 1 diabetes
topic Original Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4164068/
https://www.ncbi.nlm.nih.gov/pubmed/25337081
http://dx.doi.org/10.1159/000365481
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