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Methotrexate polyglutamates in erythrocytes are associated with lower disease activity in patients with rheumatoid arthritis

  • Maurits C. F. J. de Rotte*
  • , Ethan den Boer
  • , Pascal H. P. de Jong
  • , Saskia M. F. Pluijm
  • , Maja Bulatovic
  • , Angelique E. Weel
  • , A. Margriet Huisman
  • , Andreas H. Gerards
  • , Barbara van Schaeybroeck
  • , Nico W. Wulffraat
  • , Jan Lindemans
  • , Johanna M. W. Hazes
  • , Robert de Jonge
  • *Corresponding author for this work

Research output: Contribution to journal › Article › Academic › peer-review

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Abstract

Objective To investigate if erythrocyte-methotrexate-polyglutamate (MTX-PG) concentrations in patients with rheumatoid arthritis (RA) are associated with disease activity or adverse events.

Methods We used a longitudinal study design with two cohorts. The derivation cohort included 102 and the validation cohort included 285 patients with RA on MTX. We measured erythrocyte-MTX-PG with 1-5 glutamate residues at 3 months, 6 months and 9 months after MTX start with a liquid chromatography (LC)-mass spectrometry (MS)/MS assay. Outcomes were disease activity score in 28 joints (DAS28) and adverse events. Longitudinal associations of MTX-PG concentrations after 3 months, 6 months and 9 months with DAS28 were tested with a linear mixed model adjusted for age, gender, baseline DAS28, MTX dose and comedication.

Results In the derivation cohort, mean DAS28 decreased from 4.26 (SE=0.14) at baseline to 2.72 (SE=0.13) after 9 months. Thirty per cent of patients in the derivation cohort experienced more than three adverse events after 3 months, which decreased to 18% after 9 months. In the validation cohort, DAS28 and adverse events were comparable with the derivation cohort. In the derivation cohort, MTX-PG1 (beta=-0.005), MTX-PG2 (beta=-0.022), MTX-PG3 (beta=-0.007) and total MTX-PG (beta=-0.004) were associated (p

Conclusions In this first longitudinal study, we showed that an increase in erythrocyte-MTX-PG concentration was associated with a decreased DAS28 over 9 months in two cohorts, and is therefore a potential tool for therapeutic drug monitoring of MTX in RA.

Original languageEnglish
Pages (from-to)408-414
Number of pages7
JournalAnnals of the Rheumatic Diseases
Volume74
Issue number2
DOIs
Publication statusPublished - Feb 2015

Keywords

  • PULSE METHOTREXATE
  • CLINICAL-EFFICACY
  • AMERICAN-COLLEGE
  • FOLATE PATHWAY
  • THERAPY
  • PHARMACOKINETICS
  • POLYMORPHISMS
  • VALIDATION
  • CORRELATE
  • CRITERIA

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