TY - JOUR
T1 - Methotrexate polyglutamates in erythrocytes are associated with lower disease activity in patients with rheumatoid arthritis
AU - De Rotte, Maurits C.F.J.
AU - Den Boer, Ethan
AU - De Jong, Pascal H.P.
AU - Pluijm, Saskia M.F.
AU - Bulatović Ćalasan, Maja
AU - Weel, Angelique E.
AU - Huisman, A. Margriet
AU - Gerards, Andreas H.
AU - Van Schaeybroeck, Barbara
AU - Wulffraat, Nico M.
AU - Lindemans, Jan
AU - Hazes, Johanna M.W.
AU - De Jonge, Robert
N1 - Publisher Copyright:
© 2015, BMJ Publishing Group. All rights reserved.
PY - 2015/2/1
Y1 - 2015/2/1
N2 - 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 (β=-0.005), MTX-PG2 (β=-0.022), MTX-PG3 (β=-0.007) and total MTX-PG (β=-0.004) were associated (p<0.05) with lower DAS28 over 9 months. In the validation cohort, MTX-PG2 (β=-0.015), MTX-PG3 (β=-0.010), MTX-PG4 (β=-0.008) and total MTX-PG (β=-0.003) were associated with lower DAS28 over 9 months. None of the MTX-PGs was associated with adverse events. 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.
AB - 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 (β=-0.005), MTX-PG2 (β=-0.022), MTX-PG3 (β=-0.007) and total MTX-PG (β=-0.004) were associated (p<0.05) with lower DAS28 over 9 months. In the validation cohort, MTX-PG2 (β=-0.015), MTX-PG3 (β=-0.010), MTX-PG4 (β=-0.008) and total MTX-PG (β=-0.003) were associated with lower DAS28 over 9 months. None of the MTX-PGs was associated with adverse events. 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.
UR - http://www.scopus.com/inward/record.url?scp=84921311336&partnerID=8YFLogxK
U2 - 10.1136/annrheumdis-2013-203725
DO - 10.1136/annrheumdis-2013-203725
M3 - Article
C2 - 24297383
AN - SCOPUS:84921311336
SN - 0003-4967
VL - 74
SP - 408
EP - 414
JO - Annals of the Rheumatic Diseases
JF - Annals of the Rheumatic Diseases
IS - 2
ER -