Pharmacokinetics of hydroxychloroquine in Japanese systemic lupus erythematosus patients with renal impairment.


Journal

Modern rheumatology
ISSN: 1439-7609
Titre abrégé: Mod Rheumatol
Pays: England
ID NLM: 100959226

Informations de publication

Date de publication:
25 Aug 2023
Historique:
received: 26 07 2022
revised: 26 08 2022
accepted: 06 09 2022
medline: 28 8 2023
pubmed: 17 9 2022
entrez: 16 9 2022
Statut: ppublish

Résumé

Reduction of the hydroxychloroquine (HCQ) dosage is recommended in systemic lupus erythematosus (SLE) patients with renal impairment, but a pharmacokinetics (PK) study of patients with renal impairment has not yet been performed. We investigated the PK of both single and multiple doses of HCQ and its metabolites in SLE patients with renal impairment who newly started HCQ at a daily dose of 300 mg based on an ideal body weight dosage of 6.5 mg/kg. Population PK analysis was performed using a non-linear mixed-effects model. In total, 219 samples from 21 patients were analysed. The PK of HCQ in blood after single and multiple oral administrations followed the two-compartment model. At steady state, the concentration ratio of HCQ to each metabolite was HCQ:desethylhydroxychloroquine:desethylchloroquine:bisdesethylchloroquine = 1:0.28:0.1:0.06. The HCQ concentration correlated positively with that of each metabolite. The estimated values (relative standard error) of the population PK parameters were the total clearance at 110 l/h (31%) and a central volume of distribution of 398 l (19%). Co-administration of prednisolone and age, but not renal impairment, were factors affecting the total clearance of HCQ. From the PK perspective, a dosage reduction is unnecessary in SLE patients with impaired renal function.

Identifiants

pubmed: 36112484
pii: 6702264
doi: 10.1093/mr/roac113
doi:

Substances chimiques

Antirheumatic Agents 0
Hydroxychloroquine 4QWG6N8QKH
Prednisolone 9PHQ9Y1OLM

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

953-960

Informations de copyright

© Japan College of Rheumatology 2022. Published by Oxford University Press. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.

Auteurs

Mikiko Shimizu (M)

Department of Pharmaceutics and Pharmacometrics, School of Pharmacy, Shujitsu University, Okayama, Japan.
Department of Drug Metabolism and Pharmacokinetics, Faculty of Pharmaceutical Sciences, Aomori University, Aomori, Japan.

Sumito Furudate (S)

Department of Drug Metabolism and Pharmacokinetics, Faculty of Pharmaceutical Sciences, Aomori University, Aomori, Japan.

Yoshiki Nagai (Y)

Department of Rheumatic Diseases, Tokyo Metropolitan Tama Medical Center, Tokyo, Japan.

Kota Shimada (K)

Department of Rheumatic Diseases, Tokyo Metropolitan Tama Medical Center, Tokyo, Japan.

Miho Ohshima (M)

Department of Rheumatology, Mitsui Memorial Hospital, Tokyo, Japan.

Keigo Setoguchi (K)

Department of Systemic Immunological Diseases, Tokyo Metropolitan Cancer and Infectious Diseases Center, Komagome Hospital, Tokyo, Japan.

Masayuki Hashiguchi (M)

Department of Clinical Pharmacology and Therapeutics, The Jikei University School of Medicine, Tokyo, Japan.

Naoto Yokogawa (N)

Department of Rheumatic Diseases, Tokyo Metropolitan Tama Medical Center, Tokyo, Japan.

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Classifications MeSH