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Current Clinical Pharmacology

Editor-in-Chief

ISSN (Print): 1574-8847
ISSN (Online): 2212-3938

Review Article

Hepatic Elimination of Drugs in Gestational Diabetes

Author(s): Claudio Daniel Gonzalez, Jorge Alvarinas, Ricardo Bolanos and Guillermo Di Girolamo*

Volume 13, Issue 1, 2018

Page: [21 - 27] Pages: 7

DOI: 10.2174/1574884713666180326104613

Price: $65

Abstract

Background: The liver is the major metabolic clearance organ for chemical agents from the human body.

Pregnancy is associated with several physiological changes that may affect one or more of these factors, and also induces changes in the hepatic clearance of certain drugs. The aim of this paper was to review some of the currently available information in the field to provide some insights about the relevance of these changes on the clearance of some drugs.

Methods: A comprehensive literature search was carried out to identify eligible studies from MEDLINE/PubMed, EMBASE and SCIELO databases through 1970 first semester.

Results: Gestational Diabetes Mellitus (GDM) is a frequent disease commonly associated with other entities as obesity, hypertension, dyslipidemia, non-alcoholic fatty liver disease, prothrombotic conditions, changes in intestinal microbiome. These entities, together with the glycemic fluctuations associated with GDM might affect the determinants of the hepatic clearance (hepatic blood flow, the unbound fraction of drugs, and the hepatic intrinsic clearance).

GDM is frequently associated with multi-drug treatments. While many of these drugs are cleared by the liver, little is known about the clinical relevance of these GDM associated pharmacokinetic changes.

Conclusion: Considering the frequency of the disease and the effects that these pharmacokinetic changes might have on the mother and child, the need for further research seems advisable. In the meantime, cautious clinical judgment in the management of drug administration in women affected by this disease is recommended.

Keywords: Hepatic clearance, drugs, gestational diabetes, intestinal microbiome, exogenous chemical agents, hepatocytes.

Graphical Abstract

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