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Effect of Vitamin D on Urinary Angiotensinogen Level in Early Diabetic Nephropathy

BACKGROUND: Urinary angiotensinogen (UAGT) is supposed to be a marker of activation of the intrarenal renin– angiotensin system (RAS) system in early diabetic nnephropathy (EDN). Vitamin D has been studied as a negative regulator of the circulating and tissue RAS activity, so its supplementation may...

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Autores principales: Mahapatra, Himansu Sekhar, Kumar, Adarsh, Kulshreshtha, Bindu, Chitkara, Anubhuti, Kumari, Anamika
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8443098/
https://www.ncbi.nlm.nih.gov/pubmed/34584348
http://dx.doi.org/10.4103/ijn.IJN_67_20
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author Mahapatra, Himansu Sekhar
Kumar, Adarsh
Kulshreshtha, Bindu
Chitkara, Anubhuti
Kumari, Anamika
author_facet Mahapatra, Himansu Sekhar
Kumar, Adarsh
Kulshreshtha, Bindu
Chitkara, Anubhuti
Kumari, Anamika
author_sort Mahapatra, Himansu Sekhar
collection PubMed
description BACKGROUND: Urinary angiotensinogen (UAGT) is supposed to be a marker of activation of the intrarenal renin– angiotensin system (RAS) system in early diabetic nnephropathy (EDN). Vitamin D has been studied as a negative regulator of the circulating and tissue RAS activity, so its supplementation may prevent the progression of diabetic nephropathy (DN). This study was planned to assess the RAS activation and effect of vitamin D supplementation in EDN progression by estimating the UAGT level. METHODS: A total of 103 EDN subjects were randomized in two groups to receive either cholecalciferol (54) or matching placebo (49) in a double-blind manner. All were subjected to routine investigations, urinary albumin-to-creatinine ratio (UACR), UAGT, vitamin D, and intact parathyroid hormone (iPTH) at the 0 and 6 months. A total 40 healthy controls were also included for assessment of the same investigations at 0 month. RESULTS: Significant reduction of UACR, UAGT, and iPTH level were corroborated with an increase in 25(OH) vitamin D level from 0 to 6 months (all four P < 0.001). After 6 months, the median [interquartile range (IQR)] of UAGT and UACR levels was significantly lower in the cholecalciferol group as compared to placebo group (p < 0.001 and P = 0.04, respectively). The median UAGT level was significantly higher in patients with EDN (cholecalciferol & placebo Group) than control group at 0 month (p = 0.001). CONCLUSION: Significantly higher UAGT levels in EDN supports the role of intrarenal RAS activation. A significant decrease in UAGT level in the cholecalciferol group supports the beneficial role of vitamin D supplementation in the progression of EDN.
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spelling pubmed-84430982021-09-27 Effect of Vitamin D on Urinary Angiotensinogen Level in Early Diabetic Nephropathy Mahapatra, Himansu Sekhar Kumar, Adarsh Kulshreshtha, Bindu Chitkara, Anubhuti Kumari, Anamika Indian J Nephrol Original Article BACKGROUND: Urinary angiotensinogen (UAGT) is supposed to be a marker of activation of the intrarenal renin– angiotensin system (RAS) system in early diabetic nnephropathy (EDN). Vitamin D has been studied as a negative regulator of the circulating and tissue RAS activity, so its supplementation may prevent the progression of diabetic nephropathy (DN). This study was planned to assess the RAS activation and effect of vitamin D supplementation in EDN progression by estimating the UAGT level. METHODS: A total of 103 EDN subjects were randomized in two groups to receive either cholecalciferol (54) or matching placebo (49) in a double-blind manner. All were subjected to routine investigations, urinary albumin-to-creatinine ratio (UACR), UAGT, vitamin D, and intact parathyroid hormone (iPTH) at the 0 and 6 months. A total 40 healthy controls were also included for assessment of the same investigations at 0 month. RESULTS: Significant reduction of UACR, UAGT, and iPTH level were corroborated with an increase in 25(OH) vitamin D level from 0 to 6 months (all four P < 0.001). After 6 months, the median [interquartile range (IQR)] of UAGT and UACR levels was significantly lower in the cholecalciferol group as compared to placebo group (p < 0.001 and P = 0.04, respectively). The median UAGT level was significantly higher in patients with EDN (cholecalciferol & placebo Group) than control group at 0 month (p = 0.001). CONCLUSION: Significantly higher UAGT levels in EDN supports the role of intrarenal RAS activation. A significant decrease in UAGT level in the cholecalciferol group supports the beneficial role of vitamin D supplementation in the progression of EDN. Wolters Kluwer - Medknow 2021 2021-01-27 /pmc/articles/PMC8443098/ /pubmed/34584348 http://dx.doi.org/10.4103/ijn.IJN_67_20 Text en Copyright: © 2021 Indian Journal of Nephrology https://creativecommons.org/licenses/by-nc-sa/4.0/This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms.
spellingShingle Original Article
Mahapatra, Himansu Sekhar
Kumar, Adarsh
Kulshreshtha, Bindu
Chitkara, Anubhuti
Kumari, Anamika
Effect of Vitamin D on Urinary Angiotensinogen Level in Early Diabetic Nephropathy
title Effect of Vitamin D on Urinary Angiotensinogen Level in Early Diabetic Nephropathy
title_full Effect of Vitamin D on Urinary Angiotensinogen Level in Early Diabetic Nephropathy
title_fullStr Effect of Vitamin D on Urinary Angiotensinogen Level in Early Diabetic Nephropathy
title_full_unstemmed Effect of Vitamin D on Urinary Angiotensinogen Level in Early Diabetic Nephropathy
title_short Effect of Vitamin D on Urinary Angiotensinogen Level in Early Diabetic Nephropathy
title_sort effect of vitamin d on urinary angiotensinogen level in early diabetic nephropathy
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8443098/
https://www.ncbi.nlm.nih.gov/pubmed/34584348
http://dx.doi.org/10.4103/ijn.IJN_67_20
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