Literature DB >> 19644853

Determinants of red blood cell methotrexate polyglutamate concentrations in rheumatoid arthritis patients receiving long-term methotrexate treatment.

Lisa K Stamp1, John L O'Donnell, Peter T Chapman, Mei Zhang, Christopher Frampton, Jill James, Murray L Barclay.   

Abstract

OBJECTIVE: Methotrexate (MTX) is the most commonly used disease-modifying antirheumatic drug (DMARD) in the management of rheumatoid arthritis (RA). MTX is transported into cells, where additional glutamate moieties are added and it is retained as MTX polyglutamates (MTXGlu [referred to as a group as MTXGlun]). There is large interpatient variability in MTXGlun concentrations. This study was undertaken to determine nongenetic factors that influence red blood cell (RBC) MTXGlun concentrations in patients receiving long-term stable low-dose oral MTX.
METHODS: One hundred ninety-two patients receiving long-term oral MTX for the treatment of RA were recruited. Trough MTXGlun concentrations were measured by high-performance liquid chromatography. Univariate analysis was performed to determine variables influencing MTXGlun concentrations. Backward stepwise multivariate regression analysis was done to determine variables that affect individual MTXGlun concentrations; variables with P values of <0.1 in the univariate analysis for any MTXGlun were included.
RESULTS: Univariate analysis revealed that increased age, lower estimated glomerular filtration rate (GFR), higher MTX dosage, longer duration of MTX treatment, and use of prednisone were associated with significantly higher MTXGlun concentrations. Smokers had significantly lower concentrations of MTXGlu3, MTXGlu3-5, and MTXGlu1-5. Sex, rheumatoid factor and anti-cyclic citrullinated peptide status, RBC folate level, and body mass index had no significant effect on MTXGlun levels. Concomitant use of other DMARDs was associated with lower MTXGlu2 levels, and treatment with nonsteroidal antiinflammatory drugs was associated with lower MTXGlu3 and MTXGlu1-5 concentrations. Multivariate regression analysis revealed that age, MTX dosage, and estimated GFR were the major determinants of MTXGlun concentrations.
CONCLUSION: Large interpatient variability in MTXGlun concentrations can be explained, at least in part, by a combination of factors, particularly age, MTX dosage, and renal function. There are complex interactions between smoking, RBC folate levels, and concentrations of MTXGlun.

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Year:  2009        PMID: 19644853     DOI: 10.1002/art.24653

Source DB:  PubMed          Journal:  Arthritis Rheum        ISSN: 0004-3591


  24 in total

1.  Increased sensitivity to apoptosis induced by methotrexate is mediated by JNK.

Authors:  Charles F Spurlock; Zachary T Aune; John T Tossberg; Patrick L Collins; Jessica P Aune; Joseph W Huston; Philip S Crooke; Nancy J Olsen; Thomas M Aune
Journal:  Arthritis Rheum       Date:  2011-09

2.  Phase II trial of methotrexate in myasthenia gravis.

Authors:  Mamatha Pasnoor; Jianghua He; Laura Herbelin; Mazen Dimachkie; Richard J Barohn
Journal:  Ann N Y Acad Sci       Date:  2012-12       Impact factor: 5.691

3.  [The future of methotrexate therapy and other folate inhibitors].

Authors:  C Fiehn
Journal:  Z Rheumatol       Date:  2011-02       Impact factor: 1.372

4.  Safety and Efficacy of Methotrexate for Chinese Adults With Psoriasis With and Without Psoriatic Arthritis.

Authors:  Kexiang Yan; Yuanjing Zhang; Ling Han; Qiong Huang; Zhenghua Zhang; Xu Fang; Zhizhong Zheng; Nikhil Yawalkar; Yuling Chang; Qun Zhang; Ling Jin; Danfeng Qian; Xueying Li; Mingshun Wu; Qiaohu Xu; Xuejun Zhang; Jinhua Xu
Journal:  JAMA Dermatol       Date:  2019-03-01       Impact factor: 10.282

5.  High-dose methotrexate in Egyptian pediatric acute lymphoblastic leukemia: the impact of ABCG2 C421A genetic polymorphism on plasma levels, what is next?

Authors:  Hala O El Mesallamy; Wafaa M Rashed; Nadia M Hamdy; Nayera Hamdy
Journal:  J Cancer Res Clin Oncol       Date:  2014-04-10       Impact factor: 4.553

Review 6.  Optimising low-dose methotrexate for rheumatoid arthritis-A review.

Authors:  Catherine J Lucas; Simon B Dimmitt; Jennifer H Martin
Journal:  Br J Clin Pharmacol       Date:  2019-08-09       Impact factor: 4.335

7.  Pharmacokinetics, pharmacodynamics and toxicities of methotrexate in healthy and collagen-induced arthritic rats.

Authors:  Dong-Yang Liu; Hoi-Kei Lon; Yan-Lin Wang; Debra C DuBois; Richard R Almon; William J Jusko
Journal:  Biopharm Drug Dispos       Date:  2013-04-07       Impact factor: 1.627

8.  [Personalized medicine in the choice of conventional immunosuppressants and disease modifying antirheumatic drugs].

Authors:  C Fiehn; G Keyßer; H-M Lorenz
Journal:  Z Rheumatol       Date:  2013-02       Impact factor: 1.372

9.  A population pharmacokinetic model for low-dose methotrexate and its polyglutamated metabolites in red blood cells.

Authors:  Julia Korell; Lisa K Stamp; Murray L Barclay; Judith M Dalrymple; Jill Drake; Mei Zhang; Stephen B Duffull
Journal:  Clin Pharmacokinet       Date:  2013-06       Impact factor: 6.447

10.  The concomitant use of meloxicam and methotrexate does not clearly increase the risk of silent kidney and liver damages in patients with rheumatoid arthritis.

Authors:  Hee-Jin Park; Min-Chan Park; Yong-Beom Park; Soo-Kon Lee; Sang-Won Lee
Journal:  Rheumatol Int       Date:  2013-12-22       Impact factor: 2.631

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