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Metabolic and Hormonal Determinants of Glomerular Filtration Rate and Renal Hemodynamics in Severely Obese Individuals

OBJECTIVE: Renal function is often compromised in severe obesity. A true measurement of glomerular filtration rate (GFR) is unusual, and how estimation formulae (EstForm) perform in such individuals is unclear. We characterized renal function and hemodynamics in severely obese individuals, assessing...

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Autores principales: Vitolo, Edoardo, Santini, Eleonora, Salvati, Antonio, Volterrani, Duccio, Duce, Valerio, Bruno, Rosa Maria, Solini, Anna
Formato: Online Artículo Texto
Lenguaje:English
Publicado: S. Karger GmbH 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5644791/
https://www.ncbi.nlm.nih.gov/pubmed/27701167
http://dx.doi.org/10.1159/000446965
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author Vitolo, Edoardo
Santini, Eleonora
Salvati, Antonio
Volterrani, Duccio
Duce, Valerio
Bruno, Rosa Maria
Solini, Anna
author_facet Vitolo, Edoardo
Santini, Eleonora
Salvati, Antonio
Volterrani, Duccio
Duce, Valerio
Bruno, Rosa Maria
Solini, Anna
author_sort Vitolo, Edoardo
collection PubMed
description OBJECTIVE: Renal function is often compromised in severe obesity. A true measurement of glomerular filtration rate (GFR) is unusual, and how estimation formulae (EstForm) perform in such individuals is unclear. We characterized renal function and hemodynamics in severely obese individuals, assessing the reliability of EstForm. METHODS: We measured GFR (mGFR) by iohexol plasma clearance, renal plasma flow (RPF) by (123)I-ortho-iodo-hippurate, basal and stimulated vascular renal indices, endothelium-dependent and -independent vasodilation using flow-mediated dilation (FMD) as well as metabolic and hormonal profile in morbid, otherwise healthy, obese subjects. RESULTS: Compared with mGFR, the better performing EstForm was CKD-EPI (5.3 ml/min/1.73 m(2) bias by Bland-Altman analysis). mGFR was directly related with RPF, total and incremental glucose AUC, and inversely with PTH and h8 cortisol. Patients with mGFR below the median shown significantly higher PTH and lower vitamin D3. Basal or dynamic renal resistive index, FMD, pulse wave velocity were not related with mGFR. In an adjusted regression model, renal diameter and plasma flow remained related with mGFR (R(2) = 0.67), accounting for 15s% and 21s% of mGFR variance, respectively. CONCLUSIONS: CKD-EPI formula should be preferred in morbid obesity; glucose increments during oral glucose tolerance test correlate with hyperfiltration; RPF and diameter are independent determinants of mGFR; slightly high PTH values, frequent in obesity, might influence mGFR.
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spelling pubmed-56447912017-12-04 Metabolic and Hormonal Determinants of Glomerular Filtration Rate and Renal Hemodynamics in Severely Obese Individuals Vitolo, Edoardo Santini, Eleonora Salvati, Antonio Volterrani, Duccio Duce, Valerio Bruno, Rosa Maria Solini, Anna Obes Facts Original Article OBJECTIVE: Renal function is often compromised in severe obesity. A true measurement of glomerular filtration rate (GFR) is unusual, and how estimation formulae (EstForm) perform in such individuals is unclear. We characterized renal function and hemodynamics in severely obese individuals, assessing the reliability of EstForm. METHODS: We measured GFR (mGFR) by iohexol plasma clearance, renal plasma flow (RPF) by (123)I-ortho-iodo-hippurate, basal and stimulated vascular renal indices, endothelium-dependent and -independent vasodilation using flow-mediated dilation (FMD) as well as metabolic and hormonal profile in morbid, otherwise healthy, obese subjects. RESULTS: Compared with mGFR, the better performing EstForm was CKD-EPI (5.3 ml/min/1.73 m(2) bias by Bland-Altman analysis). mGFR was directly related with RPF, total and incremental glucose AUC, and inversely with PTH and h8 cortisol. Patients with mGFR below the median shown significantly higher PTH and lower vitamin D3. Basal or dynamic renal resistive index, FMD, pulse wave velocity were not related with mGFR. In an adjusted regression model, renal diameter and plasma flow remained related with mGFR (R(2) = 0.67), accounting for 15s% and 21s% of mGFR variance, respectively. CONCLUSIONS: CKD-EPI formula should be preferred in morbid obesity; glucose increments during oral glucose tolerance test correlate with hyperfiltration; RPF and diameter are independent determinants of mGFR; slightly high PTH values, frequent in obesity, might influence mGFR. S. Karger GmbH 2016-11 2016-10-05 /pmc/articles/PMC5644791/ /pubmed/27701167 http://dx.doi.org/10.1159/000446965 Text en Copyright © 2016 by S. Karger GmbH, Freiburg http://creativecommons.org/licenses/by-nc-nd/4.0/ This article is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License (CC BY-NC-ND) (http://www.karger.com/Services/OpenAccessLicense). Usage and distribution for commercial purposes as well as any distribution of modified material requires written permission.
spellingShingle Original Article
Vitolo, Edoardo
Santini, Eleonora
Salvati, Antonio
Volterrani, Duccio
Duce, Valerio
Bruno, Rosa Maria
Solini, Anna
Metabolic and Hormonal Determinants of Glomerular Filtration Rate and Renal Hemodynamics in Severely Obese Individuals
title Metabolic and Hormonal Determinants of Glomerular Filtration Rate and Renal Hemodynamics in Severely Obese Individuals
title_full Metabolic and Hormonal Determinants of Glomerular Filtration Rate and Renal Hemodynamics in Severely Obese Individuals
title_fullStr Metabolic and Hormonal Determinants of Glomerular Filtration Rate and Renal Hemodynamics in Severely Obese Individuals
title_full_unstemmed Metabolic and Hormonal Determinants of Glomerular Filtration Rate and Renal Hemodynamics in Severely Obese Individuals
title_short Metabolic and Hormonal Determinants of Glomerular Filtration Rate and Renal Hemodynamics in Severely Obese Individuals
title_sort metabolic and hormonal determinants of glomerular filtration rate and renal hemodynamics in severely obese individuals
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5644791/
https://www.ncbi.nlm.nih.gov/pubmed/27701167
http://dx.doi.org/10.1159/000446965
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