Expression of resistance markers to methotrexate predicts clinical improvement in patients with rheumatoid arthritis
- PMID: 15345497
- PMCID: PMC1755459
- DOI: 10.1136/ard.2003.014985
Expression of resistance markers to methotrexate predicts clinical improvement in patients with rheumatoid arthritis
Abstract
Background: Methotrexate is transported into the cell by the reduced folate carrier (RFC) and out of the cell by members of the multidrug resistance protein family (MRP). Transport proteins may affect the therapeutic efficacy of this drug in patients with rheumatoid arthritis.
Objective: To investigate the potential benefit of the presence of RFC and the absence of functional MRP for the efficacy of methotrexate treatment.
Methods: The study involved 163 patients (116 female, 47 male; mean age 59.5 years) on methotrexate (mean weekly dose 12.2 mg). RFC was determined using reverse transcriptase polymerase chain reaction, and MRP function by flow cytometry, using a calcein acetoxymethylesther/probenecid assay. Clinical response to methotrexate was evaluated by the EULAR response criteria and the ACR 20% improvement criteria. The clinical data were obtained at the beginning of methotrexate treatment and at the time of blood sampling during ongoing therapy. Patients were divided into four groups according to the presence (+) or absence (-) of RFC and functional (f) MRP.
Results: fMRP+/RFC+ and fMRP-/RFC- patients more often had good EULAR response rates (60%, p = 0.014, and 53%, p = 0.035, respectively) in comparison with the fMRP-/RFC+ group (29%); fMRP+/RFC- patients had a low frequency of good disease activity responses.
Conclusions: Absence of fMRP plus presence of RFC did not prove to be related to beneficial effects of methotrexate, but the lack or the presence of both fMRP and RFC led to a significantly better therapeutic outcome. Determination of these markers may predict responsiveness to methotrexate.
Figures

Similar articles
-
Reduced folate carrier-1 80G>A polymorphism affects methotrexate treatment outcome in rheumatoid arthritis.Pharmacogenomics J. 2007 Dec;7(6):404-7. doi: 10.1038/sj.tpj.6500438. Epub 2007 Feb 27. Pharmacogenomics J. 2007. PMID: 17325736 Clinical Trial.
-
Pharmacogenetic and metabolite measurements are associated with clinical status in patients with rheumatoid arthritis treated with methotrexate: results of a multicentred cross sectional observational study.Ann Rheum Dis. 2005 Aug;64(8):1180-5. doi: 10.1136/ard.2004.033399. Epub 2005 Jan 27. Ann Rheum Dis. 2005. PMID: 15677700 Free PMC article.
-
Polyglutamation of methotrexate with common polymorphisms in reduced folate carrier, aminoimidazole carboxamide ribonucleotide transformylase, and thymidylate synthase are associated with methotrexate effects in rheumatoid arthritis.Arthritis Rheum. 2004 Sep;50(9):2766-74. doi: 10.1002/art.20460. Arthritis Rheum. 2004. PMID: 15457444
-
Sulfasalazine is a potent inhibitor of the reduced folate carrier: implications for combination therapies with methotrexate in rheumatoid arthritis.Arthritis Rheum. 2004 Jul;50(7):2130-9. doi: 10.1002/art.20375. Arthritis Rheum. 2004. PMID: 15248210
-
Predictive genetic biomarkers for the efficacy of methotrexate in rheumatoid arthritis: a systematic review.Pharmacogenomics J. 2020 Apr;20(2):159-168. doi: 10.1038/s41397-019-0098-9. Epub 2019 Oct 17. Pharmacogenomics J. 2020. PMID: 31624331
Cited by
-
The advances of methotrexate resistance in rheumatoid arthritis.Inflammopharmacology. 2020 Oct;28(5):1183-1193. doi: 10.1007/s10787-020-00741-3. Epub 2020 Aug 5. Inflammopharmacology. 2020. PMID: 32757110 Review.
-
Down regulation of multidrug resistance protein-1 expression in patients with early rheumatoid arthritis exposed to methotrexate as a first disease-modifying antirheumatic drug.Ann Rheum Dis. 2006 Oct;65(10):1390-3. doi: 10.1136/ard.2005.049189. Epub 2006 Feb 27. Ann Rheum Dis. 2006. PMID: 16504991 Free PMC article.
-
ATR and CDK4/6 inhibition target the growth of methotrexate-resistant choriocarcinoma.Oncogene. 2022 Apr;41(18):2540-2554. doi: 10.1038/s41388-022-02251-8. Epub 2022 Mar 18. Oncogene. 2022. PMID: 35301407 Free PMC article.
-
Expression of multidrug resistance-1 protein correlates with disease activity rather than the refractoriness to methotrexate therapy in rheumatoid arthritis.Clin Rheumatol. 2009 Apr;28(4):427-33. doi: 10.1007/s10067-008-1071-1. Epub 2009 Jan 10. Clin Rheumatol. 2009. PMID: 19137355
-
Predicting methotrexate resistance in rheumatoid arthritis patients.Inflammopharmacology. 2018 Jun;26(3):699-708. doi: 10.1007/s10787-018-0459-z. Epub 2018 Mar 12. Inflammopharmacology. 2018. PMID: 29532212 Review.
References
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Medical