Please use this identifier to cite or link to this item: http://hdl.handle.net/2440/76267
Citations
Scopus Web of Science® Altmetric
?
?
Type: Journal article
Title: Polymorphisms in cytochrome P450 2C19 enzyme and cessation of leflunomide in patients with rheumatoid arthritis
Author: Wiese, M.
Schnabl, M.
O'Doherty, C.
Spargo, L.
Sorich, M.
Cleland, L.
Proudman, S.
Citation: Arthritis Research & Therapy, 2012; 14(4):1-9
Publisher: BioMed Central Ltd.
Issue Date: 2012
ISSN: 1478-6354
1478-6362
Statement of
Responsibility: 
Michael D Wiese, Matthew Schnabl, Catherine O’Doherty, Llewellyn D Spargo, Michael J Sorich, Leslie G Cleland and Susanna M Proudman
Abstract: Introduction: Rational selection of disease modifying anti-rheumatic drugs in the treatment of rheumatoid arthritis (RA) has many potential advantages, including rapid disease control, reduced long-term disability and reduced overall cost to the healthcare system. Inter-individual genetic differences are particularly attractive as markers to predict efficacy and toxicity, as they can be determined rapidly prior to drug selection. The aims of this study, therefore, were to investigate the association between differences in genes associated with the metabolism, clearance and efficacy of leflunomide with its cessation in a group of rheumatoid arthritis patients who were treated with an intensive contemporary, treat-to-target approach. Methods: This retrospective cohort study identified all individuals who received leflunomide and were enrolled in the Early Arthritis inception cohort at the Royal Adelaide Hospital between 2001 and July 2011. Inclusion criteria were age (>18) and a diagnosis of rheumatoid arthritis. Patients were excluded if a DNA sample was not available, if they withdrew from the cohort or if clinical data were insufficient. Subjects were followed for 12 months or until either another disease modifying antirheumatic drug was added or leflunomide was ceased. The following single nucleotide polymorphisms (SNPs) were determined: CYP2C19*2 (rs4244285), CYP2C19*17 (rs12248560), ABCG2 421C>A (rs2231142), CYP1A2*1F (rs762551) and DHODH 19C>A (rs3213422). The effects of variables on cessation were assessed with Cox Proportional Hazard models. Results: Thirty-three of 78 (42.3%) patients ceased leflunomide due to side effects. A linear trend between cytochrome P450 2C19 (CYP2C19) phenotype and leflunomide cessation was observed, with poor and intermediate metabolizers ceasing more frequently (adjusted Hazard Ratio = 0.432 for each incremental change in phenotype, 95% CI 0.237 to 0.790, P = 0.006). Previously observed associations between cytochrome P450 1A2 (CYP1A2) and dihydro-orotate dehydrogenase (DHODH) genotype and toxicity were not apparent, but there was a trend for ATP-binding cassette sub-family G member 2 (ABCG2) genotype to be associated with cessation due to diarrhea. Conclusions: CYP2C19 phenotype was associated with cessation due to toxicity, and since CYP2C19 intermediate and poor metabolizers have lower teriflunomide concentrations, it is likely that they have a particularly poor risk:benefit ratio when using this drug.
Keywords: Humans; Arthritis, Rheumatoid; Diarrhea; Isoxazoles; Antirheumatic Agents; Withholding Treatment; Retrospective Studies; Cohort Studies; Follow-Up Studies; Polymorphism, Single Nucleotide; Aged; Middle Aged; Female; Male; Cytochrome P-450 CYP2C19
Description: Extent: 9p.
Rights: © 2012 Wiese et al.; licensee BioMed Central Ltd.This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
RMID: 0020124224
DOI: 10.1186/ar3911
Appears in Collections:Medicine publications

Files in This Item:
File Description SizeFormat 
hdl_76267.pdfPublished version261.38 kBAdobe PDFView/Open


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.