Therapeutic drug monitoring of teriflunomide: do plasma concentrations predict response to leflunomide in patients with rheumatoid arthritis?


Journal

Drug metabolism and personalized therapy
ISSN: 2363-8915
Titre abrégé: Drug Metab Pers Ther
Pays: Germany
ID NLM: 101653409

Informations de publication

Date de publication:
01 03 2023
Historique:
received: 07 01 2022
accepted: 01 06 2022
pubmed: 24 8 2022
medline: 17 3 2023
entrez: 23 8 2022
Statut: epublish

Résumé

Leflunomide is a commonly used treatment for rheumatoid arthritis. It acts by inhibiting dihydroorotate dehydrogenase through its active metabolite teriflunomide. The objective of the study was to investigate the relation between plasma-concentration of teriflunomide and disease-activity in rheumatoid arthritis. Data were collected from patients with rheumatoid arthritis on a stable leflunomide dose for at least 2 months. Socio-demographic data, disease characteristics and DAS28 score were recorded. Blood samples were taken for determination of teriflunomide concentration. A total of 32 serum concentration-time measurements were collected. The concentration of teriflunomide was positively correlated with disease duration of RA (r We did not find a concentration-effect-relationship. However, therapeutic drug monitoring of teriflunomide may be useful to ensure adherence and evaluate toxic-levels in case of adverse-events.

Identifiants

pubmed: 35998916
pii: dmdi-2021-0236
doi: 10.1515/dmpt-2021-0236
doi:

Substances chimiques

Leflunomide G162GK9U4W
teriflunomide 1C058IKG3B
Isoxazoles 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

79-85

Informations de copyright

© 2022 Walter de Gruyter GmbH, Berlin/Boston.

Références

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Auteurs

Tekaya Rawdha (T)

Rheumatology Department, Charles Nicolle Hospital, Tunis, Tunisia.
Faculty of Medicine of Tunis, University Tunis El Manar, Tunis, Tunisia.

Ben Tekaya Aicha (BT)

Rheumatology Department, Charles Nicolle Hospital, Tunis, Tunisia.
Faculty of Medicine of Tunis, University Tunis El Manar, Tunis, Tunisia.

Ben Ammar Lobna (BA)

Rheumatology Department, Charles Nicolle Hospital, Tunis, Tunisia.

Salouaje Issam (S)

Faculty of Medicine of Tunis, University Tunis El Manar, Tunis, Tunisia.
Department of Clinical Pharmacology, National Centre of Pharmacovigilance, Tunis, Tunisia.

Ben Sassi Mouna (BS)

Faculty of Medicine of Tunis, University Tunis El Manar, Tunis, Tunisia.
Department of Clinical Pharmacology, National Centre of Pharmacovigilance, Tunis, Tunisia.

Saidane Olfa (S)

Rheumatology Department, Charles Nicolle Hospital, Tunis, Tunisia.
Faculty of Medicine of Tunis, University Tunis El Manar, Tunis, Tunisia.

Bouden Selma (B)

Rheumatology Department, Charles Nicolle Hospital, Tunis, Tunisia.
Faculty of Medicine of Tunis, University Tunis El Manar, Tunis, Tunisia.

Ben Brahim Takoua (BB)

Department of Clinical Pharmacology, National Centre of Pharmacovigilance, Tunis, Tunisia.

Ben Abdelghani Kawther (BA)

Faculty of Medicine of Tunis, University Tunis El Manar, Tunis, Tunisia.
Rheumatology Department, Mongi Slim Hospital, Marsa, Tunisia.

Metoui Leila (M)

Faculty of Medicine of Tunis, University Tunis El Manar, Tunis, Tunisia.
Rheumatology Department, Tunis Military Hospital, Tunis, Tunisia.

Sahli Hana (S)

Faculty of Medicine of Tunis, University Tunis El Manar, Tunis, Tunisia.
Medicine Department, Hospital Tahar Maamouri, Nabeul, Tunisia.

Mahmoud Ines (M)

Rheumatology Department, Charles Nicolle Hospital, Tunis, Tunisia.
Faculty of Medicine of Tunis, University Tunis El Manar, Tunis, Tunisia.

Abdelmoula Leila (A)

Rheumatology Department, Charles Nicolle Hospital, Tunis, Tunisia.
Faculty of Medicine of Tunis, University Tunis El Manar, Tunis, Tunisia.

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