Glucocorticoids dosing in obese subjects: A systematic review.


Journal

Therapie
ISSN: 1958-5578
Titre abrégé: Therapie
Pays: France
ID NLM: 0420544

Informations de publication

Date de publication:
Sep 2019
Historique:
received: 13 07 2018
revised: 08 10 2018
accepted: 19 11 2018
pubmed: 1 4 2019
medline: 6 2 2020
entrez: 1 4 2019
Statut: ppublish

Résumé

Glucocorticoids (GCs) are amongst the most widely used and effective treatments to control inflammatory and autoimmune diseases. In obese subjects, drug dosing adjusted by body weight is problematic, all the more so as patients are at higher risk of GC metabolic side effects. We propose here to describe the determinants of drug pharmacokinetics (PK) in obese subjects and GC pharmacology, and to identify the existing PK studies that may help discussing the best size descriptor for GC dosing in obese subjects. A clinician and a pharmacist screened PubMed using the MeSH Terms: "glucocorticoids" OR "steroidal agents" AND "pharmacokinetics" AND "obesity" OR "overweight". The search was limited to the publications written in English language and to those performed in humans. A systematic search using the MeSH terms was performed until August 31st, 2017. Only three such PK studies have been published so far that compare dexamethasone, prednisolone and methylprednisolone in obese and normal weight subjects. The studies concur that GC partially distribute in the excess of body weight and that adjustment by total body weight (TBW) or by body weight (BW) excess would increase the initial plasma GC concentration after a loading dose and would thus be inappropriate. Contradictory results are observed regarding GC exposure or clearance according to the GC studied. Behind this overwhelming lack of conclusive evidence for adjusting GC by body weight, further PK studies are clearly needed for guiding their dosing. Furthermore, studies demonstrated an increased sensibility to GC, even when GC exposure was reduced, suggesting that adjustment by body weight may not only be unnecessary but also dangerous.

Identifiants

pubmed: 30928086
pii: S0040-5957(19)30031-9
doi: 10.1016/j.therap.2018.11.016
pii:
doi:

Substances chimiques

Glucocorticoids 0

Types de publication

Journal Article Systematic Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

451-458

Informations de copyright

Copyright © 2019. Published by Elsevier Masson SAS.

Auteurs

Jérémie Delaleu (J)

Assistance Publique-Hôpitaux de Paris, Hôpital Lariboisière, Department of Internal Medicine, 75010 Paris, France.

Alexandre Destere (A)

CHU de Limoges, Department of Pharmacology and Toxicology, 87000 Limoges, France.

Lorry Hachon (L)

Assistance Publique-Hôpitaux de Paris (AP-HP), Pharmacy Department, Hôpital Cochin, 75014 Paris, France.

Xavier Declèves (X)

INSERM, UMR-S 1144 Université Paris Descartes-Paris Diderot, variabilité de réponse aux psychotropes, 75006 Paris, France; Assistance Publique-Hôpitaux de Paris, Hôpital Cochin, Pharmacokinetics and Pharmacochemistry Unit, 75014 Paris, France.

Célia Lloret-Linares (C)

Groupe Ramsay-Générale de Santé, Hôpital Privé Pays de Savoie, Maladies Nutritionnelles et Métaboliques, 74100 Annemasse, France. Electronic address: celialloret@yahoo.fr.

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH