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Rifampicin Alters Metformin Plasma Exposure but Not Blood Glucose Levels in Diabetic Tuberculosis Patients

The pharmacokinetic (PK) and clinical implications of combining metformin with rifampicin are relevant to increasing numbers of patients with diabetic tuberculosis (TB) across the world and are yet unclear. We assessed the impact of rifampicin on metformin PKs and its glucose‐lowering effect in pati...

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Autores principales: te Brake, Lindsey H.M., Yunivita, Vycke, Livia, Resvi, Soetedjo, Nanny, van Ewijk‐Beneken Kolmer, Eleonora, Koenderink, Jan B., Burger, David M., Santoso, Prayudi, van Crevel, Reinout, Alisjahbana, Bachti, Aarnoutse, Rob E., Ruslami, Rovina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6587702/
https://www.ncbi.nlm.nih.gov/pubmed/30222857
http://dx.doi.org/10.1002/cpt.1232
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author te Brake, Lindsey H.M.
Yunivita, Vycke
Livia, Resvi
Soetedjo, Nanny
van Ewijk‐Beneken Kolmer, Eleonora
Koenderink, Jan B.
Burger, David M.
Santoso, Prayudi
van Crevel, Reinout
Alisjahbana, Bachti
Aarnoutse, Rob E.
Ruslami, Rovina
author_facet te Brake, Lindsey H.M.
Yunivita, Vycke
Livia, Resvi
Soetedjo, Nanny
van Ewijk‐Beneken Kolmer, Eleonora
Koenderink, Jan B.
Burger, David M.
Santoso, Prayudi
van Crevel, Reinout
Alisjahbana, Bachti
Aarnoutse, Rob E.
Ruslami, Rovina
author_sort te Brake, Lindsey H.M.
collection PubMed
description The pharmacokinetic (PK) and clinical implications of combining metformin with rifampicin are relevant to increasing numbers of patients with diabetic tuberculosis (TB) across the world and are yet unclear. We assessed the impact of rifampicin on metformin PKs and its glucose‐lowering effect in patients with diabetic TB by measuring plasma metformin and blood glucose during and after TB treatment. Rifampicin increased metformin exposure: plasma area under the plasma concentration‐time curve from time point 0 to the end of the dosing interval (AUC (0–τ)) and peak plasma concentration (C(max)) geometric mean ratio (GMR; during vs. after TB treatment) were 1.28 (90% confidence interval (CI) 1.13–1.44) and 1.19 (90% CI 1.02–1.38; n = 22). The metformin glucose‐lowering efficacy did not change (Δglucose − C(max); P = 0.890; n = 18). Thus, we conclude that additional glucose monitoring in this population is not warranted. Finally, 57% of patients on metformin and rifampicin, and 38% of patients on metformin alone experienced gastrointestinal adverse effects. Considering this observation, we advise patients to take metformin and rifampicin with food and preferably separated in time. Clinicians could consider metoclopramide if gastrointestinal adverse effects occur.
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spelling pubmed-65877022019-07-08 Rifampicin Alters Metformin Plasma Exposure but Not Blood Glucose Levels in Diabetic Tuberculosis Patients te Brake, Lindsey H.M. Yunivita, Vycke Livia, Resvi Soetedjo, Nanny van Ewijk‐Beneken Kolmer, Eleonora Koenderink, Jan B. Burger, David M. Santoso, Prayudi van Crevel, Reinout Alisjahbana, Bachti Aarnoutse, Rob E. Ruslami, Rovina Clin Pharmacol Ther Research The pharmacokinetic (PK) and clinical implications of combining metformin with rifampicin are relevant to increasing numbers of patients with diabetic tuberculosis (TB) across the world and are yet unclear. We assessed the impact of rifampicin on metformin PKs and its glucose‐lowering effect in patients with diabetic TB by measuring plasma metformin and blood glucose during and after TB treatment. Rifampicin increased metformin exposure: plasma area under the plasma concentration‐time curve from time point 0 to the end of the dosing interval (AUC (0–τ)) and peak plasma concentration (C(max)) geometric mean ratio (GMR; during vs. after TB treatment) were 1.28 (90% confidence interval (CI) 1.13–1.44) and 1.19 (90% CI 1.02–1.38; n = 22). The metformin glucose‐lowering efficacy did not change (Δglucose − C(max); P = 0.890; n = 18). Thus, we conclude that additional glucose monitoring in this population is not warranted. Finally, 57% of patients on metformin and rifampicin, and 38% of patients on metformin alone experienced gastrointestinal adverse effects. Considering this observation, we advise patients to take metformin and rifampicin with food and preferably separated in time. Clinicians could consider metoclopramide if gastrointestinal adverse effects occur. John Wiley and Sons Inc. 2018-10-29 2019-03 /pmc/articles/PMC6587702/ /pubmed/30222857 http://dx.doi.org/10.1002/cpt.1232 Text en © 2018 The Authors Clinical Pharmacology & Therapeutics published by Wiley Periodicals, Inc. on behalf of American Society for Clinical Pharmacology and Therapeutics This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Research
te Brake, Lindsey H.M.
Yunivita, Vycke
Livia, Resvi
Soetedjo, Nanny
van Ewijk‐Beneken Kolmer, Eleonora
Koenderink, Jan B.
Burger, David M.
Santoso, Prayudi
van Crevel, Reinout
Alisjahbana, Bachti
Aarnoutse, Rob E.
Ruslami, Rovina
Rifampicin Alters Metformin Plasma Exposure but Not Blood Glucose Levels in Diabetic Tuberculosis Patients
title Rifampicin Alters Metformin Plasma Exposure but Not Blood Glucose Levels in Diabetic Tuberculosis Patients
title_full Rifampicin Alters Metformin Plasma Exposure but Not Blood Glucose Levels in Diabetic Tuberculosis Patients
title_fullStr Rifampicin Alters Metformin Plasma Exposure but Not Blood Glucose Levels in Diabetic Tuberculosis Patients
title_full_unstemmed Rifampicin Alters Metformin Plasma Exposure but Not Blood Glucose Levels in Diabetic Tuberculosis Patients
title_short Rifampicin Alters Metformin Plasma Exposure but Not Blood Glucose Levels in Diabetic Tuberculosis Patients
title_sort rifampicin alters metformin plasma exposure but not blood glucose levels in diabetic tuberculosis patients
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6587702/
https://www.ncbi.nlm.nih.gov/pubmed/30222857
http://dx.doi.org/10.1002/cpt.1232
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