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Pharmacokinetics of metformin in patients with chronic kidney disease stage 4 and metformin‐naïve type 2 diabetes
The pharmacokinetics of metformin therapy in patients with chronic kidney disease stage 4 (CKD‐4) were studied using data from the largest Phase I consecutive cohort trial yet performed in this population. Eighteen metformin‐naïve men and women with Type 2 Diabetes and creatinine clearance (CrCl) in...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6138239/ https://www.ncbi.nlm.nih.gov/pubmed/30221006 http://dx.doi.org/10.1002/prp2.424 |
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author | Dissanayake, Ajith M. Wheldon, Mark C. Hood, Christopher J. |
author_facet | Dissanayake, Ajith M. Wheldon, Mark C. Hood, Christopher J. |
author_sort | Dissanayake, Ajith M. |
collection | PubMed |
description | The pharmacokinetics of metformin therapy in patients with chronic kidney disease stage 4 (CKD‐4) were studied using data from the largest Phase I consecutive cohort trial yet performed in this population. Eighteen metformin‐naïve men and women with Type 2 Diabetes and creatinine clearance (CrCl) in the range 18‐49 mL/min (eGFR 15‐29 mL/min/1.73 m(2)) were allocated to daily immediate‐release metformin of 250 mg, 500 mg, or 1000 mg. A first‐dose profile and trough concentrations for 4 weeks were taken on all patients. Pharmacokinetic (PK) parameters were estimated by fitting a first‐order compartment model with absorption in a peripheral compartment to concentrations measured 24 hours post–first dose. Single‐dose PK parameters time to maximum concentration (t (max)) and maximum concentration (C (max)) were consistent with previous observations in patients with normal renal function (healthy and diabetic), as was the association between CrCl and apparent total oral clearance (Cl/F). However, patients with a CrCl below 32 mL/min had trough concentrations that were consistently above the steady‐state minimum implied by the population PK model. This suggests the model may not apply to patients with CrCl below 32 mL/min. Metformin in doses of 500‐1000 mg/day could be taken by CKD‐4 patients. However, the single‐compartment model breaks down as CrCl declines below 32 mL/min suggesting that metformin levels should be monitored regularly in progressive stage 4 CKD. |
format | Online Article Text |
id | pubmed-6138239 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-61382392018-09-15 Pharmacokinetics of metformin in patients with chronic kidney disease stage 4 and metformin‐naïve type 2 diabetes Dissanayake, Ajith M. Wheldon, Mark C. Hood, Christopher J. Pharmacol Res Perspect Original Articles The pharmacokinetics of metformin therapy in patients with chronic kidney disease stage 4 (CKD‐4) were studied using data from the largest Phase I consecutive cohort trial yet performed in this population. Eighteen metformin‐naïve men and women with Type 2 Diabetes and creatinine clearance (CrCl) in the range 18‐49 mL/min (eGFR 15‐29 mL/min/1.73 m(2)) were allocated to daily immediate‐release metformin of 250 mg, 500 mg, or 1000 mg. A first‐dose profile and trough concentrations for 4 weeks were taken on all patients. Pharmacokinetic (PK) parameters were estimated by fitting a first‐order compartment model with absorption in a peripheral compartment to concentrations measured 24 hours post–first dose. Single‐dose PK parameters time to maximum concentration (t (max)) and maximum concentration (C (max)) were consistent with previous observations in patients with normal renal function (healthy and diabetic), as was the association between CrCl and apparent total oral clearance (Cl/F). However, patients with a CrCl below 32 mL/min had trough concentrations that were consistently above the steady‐state minimum implied by the population PK model. This suggests the model may not apply to patients with CrCl below 32 mL/min. Metformin in doses of 500‐1000 mg/day could be taken by CKD‐4 patients. However, the single‐compartment model breaks down as CrCl declines below 32 mL/min suggesting that metformin levels should be monitored regularly in progressive stage 4 CKD. John Wiley and Sons Inc. 2018-09-14 /pmc/articles/PMC6138239/ /pubmed/30221006 http://dx.doi.org/10.1002/prp2.424 Text en © 2018 The Authors. Pharmacology Research & Perspectives published by John Wiley & Sons Ltd, British Pharmacological Society and American Society for Pharmacology and Experimental Therapeutics. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Articles Dissanayake, Ajith M. Wheldon, Mark C. Hood, Christopher J. Pharmacokinetics of metformin in patients with chronic kidney disease stage 4 and metformin‐naïve type 2 diabetes |
title | Pharmacokinetics of metformin in patients with chronic kidney disease stage 4 and metformin‐naïve type 2 diabetes |
title_full | Pharmacokinetics of metformin in patients with chronic kidney disease stage 4 and metformin‐naïve type 2 diabetes |
title_fullStr | Pharmacokinetics of metformin in patients with chronic kidney disease stage 4 and metformin‐naïve type 2 diabetes |
title_full_unstemmed | Pharmacokinetics of metformin in patients with chronic kidney disease stage 4 and metformin‐naïve type 2 diabetes |
title_short | Pharmacokinetics of metformin in patients with chronic kidney disease stage 4 and metformin‐naïve type 2 diabetes |
title_sort | pharmacokinetics of metformin in patients with chronic kidney disease stage 4 and metformin‐naïve type 2 diabetes |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6138239/ https://www.ncbi.nlm.nih.gov/pubmed/30221006 http://dx.doi.org/10.1002/prp2.424 |
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