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Acute renal effects of the GLP-1 receptor agonist exenatide in overweight type 2 diabetes patients: a randomised, double-blind, placebo-controlled trial
AIMS/HYPOTHESIS: This study aimed to investigate the acute renal effects of the glucagon-like peptide-1 receptor agonist (GLP-1RA) exenatide in type 2 diabetes patients. METHODS: We included overweight (BMI 25–40 kg/m(2)) men and postmenopausal women, aged 35–75 years with type 2 diabetes (HbA(1c) 4...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4901099/ https://www.ncbi.nlm.nih.gov/pubmed/27038451 http://dx.doi.org/10.1007/s00125-016-3938-z |
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author | Tonneijck, Lennart Smits, Mark M. Muskiet, Marcel H. A. Hoekstra, Trynke Kramer, Mark H. H. Danser, A. H. Jan Diamant, Michaela Joles, Jaap A. van Raalte, Daniël H. |
author_facet | Tonneijck, Lennart Smits, Mark M. Muskiet, Marcel H. A. Hoekstra, Trynke Kramer, Mark H. H. Danser, A. H. Jan Diamant, Michaela Joles, Jaap A. van Raalte, Daniël H. |
author_sort | Tonneijck, Lennart |
collection | PubMed |
description | AIMS/HYPOTHESIS: This study aimed to investigate the acute renal effects of the glucagon-like peptide-1 receptor agonist (GLP-1RA) exenatide in type 2 diabetes patients. METHODS: We included overweight (BMI 25–40 kg/m(2)) men and postmenopausal women, aged 35–75 years with type 2 diabetes (HbA(1c) 48–75 mmol/mol; 6.5–9.0%) and estimated GFR ≥ 60 ml min(−1) 1.73 m(−2). Exenatide or placebo (NaCl solution, 154 mmol/l) was administrated intravenously in an acute, randomised, double-blind, placebo-controlled trial conducted at the Diabetes Center VU University Medical Center (VUMC). GFR (primary endpoint) and effective renal plasma flow (ERPF) were determined by inulin and para-aminohippurate clearance, respectively, based on timed urine sampling. Filtration fraction (FF) and effective renal vascular resistance (ERVR) were calculated, and glomerular hydrostatic pressure (P(GLO)) and vascular resistance of the afferent (R(A)) and efferent (R(E)) renal arteriole were estimated. Tubular function was assessed by absolute and fractional excretion of sodium (FE(Na)), potassium (FE(K)) and urea (FE(U)), in addition to urine osmolality, pH and free water clearance. Renal damage markers, BP and plasma glucose were also determined. RESULTS: Of the 57 patients randomised by computer, 52 were included in the final analyses. Exenatide (n = 24) did not affect GFR (mean difference +2 ± 3 ml min(−1) 1.73 m(−2), p = 0.489), ERPF, FF, ERVR or P(GLO), compared with placebo (n = 28). Exenatide increased R(A) (p < 0.05), but did not change R(E). Exenatide increased FE(Na), FE(K), urine osmolality and pH, while FE(U), urinary flow and free water clearance were decreased (all p < 0.05). Osmolar clearance and renal damage makers were not affected. Diastolic BP and mean arterial pressure increased by 3 ± 1 and 6 ± 2 mmHg, respectively, whereas plasma glucose decreased by 1.4 ± 0.1 mmol/l (all p < 0.05). CONCLUSIONS/INTERPRETATION: Exenatide infusion does not acutely affect renal haemodynamics in overweight type 2 diabetes patients at normal filtration levels. Furthermore, acute GLP-1RA administration increases proximal sodium excretion in these patients. TRIAL REGISTRATION: ClincialTrials.gov NCT01744236 FUNDING: The research leading to these results has been funded from: (1) the European Community’s Seventh Framework Programme (FP7/2007-2013) under grant agreement number 282521 – the SAFEGUARD project; and (2) the Dutch Kidney Foundation, under grant agreement IP12.87. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s00125-016-3938-z) contains peer-reviewed but unedited supplementary material, which is available to authorised users. |
format | Online Article Text |
id | pubmed-4901099 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-49010992016-06-27 Acute renal effects of the GLP-1 receptor agonist exenatide in overweight type 2 diabetes patients: a randomised, double-blind, placebo-controlled trial Tonneijck, Lennart Smits, Mark M. Muskiet, Marcel H. A. Hoekstra, Trynke Kramer, Mark H. H. Danser, A. H. Jan Diamant, Michaela Joles, Jaap A. van Raalte, Daniël H. Diabetologia Article AIMS/HYPOTHESIS: This study aimed to investigate the acute renal effects of the glucagon-like peptide-1 receptor agonist (GLP-1RA) exenatide in type 2 diabetes patients. METHODS: We included overweight (BMI 25–40 kg/m(2)) men and postmenopausal women, aged 35–75 years with type 2 diabetes (HbA(1c) 48–75 mmol/mol; 6.5–9.0%) and estimated GFR ≥ 60 ml min(−1) 1.73 m(−2). Exenatide or placebo (NaCl solution, 154 mmol/l) was administrated intravenously in an acute, randomised, double-blind, placebo-controlled trial conducted at the Diabetes Center VU University Medical Center (VUMC). GFR (primary endpoint) and effective renal plasma flow (ERPF) were determined by inulin and para-aminohippurate clearance, respectively, based on timed urine sampling. Filtration fraction (FF) and effective renal vascular resistance (ERVR) were calculated, and glomerular hydrostatic pressure (P(GLO)) and vascular resistance of the afferent (R(A)) and efferent (R(E)) renal arteriole were estimated. Tubular function was assessed by absolute and fractional excretion of sodium (FE(Na)), potassium (FE(K)) and urea (FE(U)), in addition to urine osmolality, pH and free water clearance. Renal damage markers, BP and plasma glucose were also determined. RESULTS: Of the 57 patients randomised by computer, 52 were included in the final analyses. Exenatide (n = 24) did not affect GFR (mean difference +2 ± 3 ml min(−1) 1.73 m(−2), p = 0.489), ERPF, FF, ERVR or P(GLO), compared with placebo (n = 28). Exenatide increased R(A) (p < 0.05), but did not change R(E). Exenatide increased FE(Na), FE(K), urine osmolality and pH, while FE(U), urinary flow and free water clearance were decreased (all p < 0.05). Osmolar clearance and renal damage makers were not affected. Diastolic BP and mean arterial pressure increased by 3 ± 1 and 6 ± 2 mmHg, respectively, whereas plasma glucose decreased by 1.4 ± 0.1 mmol/l (all p < 0.05). CONCLUSIONS/INTERPRETATION: Exenatide infusion does not acutely affect renal haemodynamics in overweight type 2 diabetes patients at normal filtration levels. Furthermore, acute GLP-1RA administration increases proximal sodium excretion in these patients. TRIAL REGISTRATION: ClincialTrials.gov NCT01744236 FUNDING: The research leading to these results has been funded from: (1) the European Community’s Seventh Framework Programme (FP7/2007-2013) under grant agreement number 282521 – the SAFEGUARD project; and (2) the Dutch Kidney Foundation, under grant agreement IP12.87. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s00125-016-3938-z) contains peer-reviewed but unedited supplementary material, which is available to authorised users. Springer Berlin Heidelberg 2016-04-01 2016 /pmc/articles/PMC4901099/ /pubmed/27038451 http://dx.doi.org/10.1007/s00125-016-3938-z Text en © The Author(s) 2016 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. |
spellingShingle | Article Tonneijck, Lennart Smits, Mark M. Muskiet, Marcel H. A. Hoekstra, Trynke Kramer, Mark H. H. Danser, A. H. Jan Diamant, Michaela Joles, Jaap A. van Raalte, Daniël H. Acute renal effects of the GLP-1 receptor agonist exenatide in overweight type 2 diabetes patients: a randomised, double-blind, placebo-controlled trial |
title | Acute renal effects of the GLP-1 receptor agonist exenatide in overweight type 2 diabetes patients: a randomised, double-blind, placebo-controlled trial |
title_full | Acute renal effects of the GLP-1 receptor agonist exenatide in overweight type 2 diabetes patients: a randomised, double-blind, placebo-controlled trial |
title_fullStr | Acute renal effects of the GLP-1 receptor agonist exenatide in overweight type 2 diabetes patients: a randomised, double-blind, placebo-controlled trial |
title_full_unstemmed | Acute renal effects of the GLP-1 receptor agonist exenatide in overweight type 2 diabetes patients: a randomised, double-blind, placebo-controlled trial |
title_short | Acute renal effects of the GLP-1 receptor agonist exenatide in overweight type 2 diabetes patients: a randomised, double-blind, placebo-controlled trial |
title_sort | acute renal effects of the glp-1 receptor agonist exenatide in overweight type 2 diabetes patients: a randomised, double-blind, placebo-controlled trial |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4901099/ https://www.ncbi.nlm.nih.gov/pubmed/27038451 http://dx.doi.org/10.1007/s00125-016-3938-z |
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