4.5 Article

A meta-analysis of methotrexate polyglutamates in relation to efficacy and toxicity of methotrexate in inflammatory arthritis, colitis and dermatitis

Journal

BRITISH JOURNAL OF CLINICAL PHARMACOLOGY
Volume 89, Issue 1, Pages 61-79

Publisher

WILEY
DOI: 10.1111/bcp.15579

Keywords

immune-mediated inflammatory diseases; methotrexate; pharmacodynamics; therapeutic drug monitoring

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This study investigates the relationship between MTX-PG concentration and disease activity in RA, JIA, and psoriasis. Higher concentrations of MTX-PG are significantly associated with lower disease activity. These findings are important for the implementation of TDM in the treatment of various IMIDs.
AimsIn immune-mediated inflammatory diseases (IMIDs), early symptom control is a key therapeutic goal. Methotrexate (MTX) is the first-line treatment across IMIDs. However, MTX is underutilized and suboptimally dosed, partly due to the inability of making individualized treatment decisions through therapeutic drug monitoring (TDM). To implement TDM in clinical practice, establishing a relationship between drug concentration and disease activity is paramount. In this meta-analysis, we investigated the relationship between concentrations of MTX polyglutamates (MTX-PG) in erythrocytes and efficacy as well as toxicity across IMIDs. MethodsStudies analysing MTX-PG in relation to disease activity and/or toxicity were included for inflammatory arthritis (rheumatoid [RA] and juvenile idiopathic arthritis [JIA]), inflammatory bowel disease (Crohn's and ulcerative colitis) and dermatitis (psoriasis and atopic dermatitis). Meta-analyses were performed resulting in several summary effect measures: regression coefficient (beta), correlation coefficient and mean difference (of MTX-PG in responders vs. nonresponders) for IMIDs separately and collectively. ResultsTwenty-five studies were included. In RA and JIA, higher MTX-PG was significantly associated with lower disease activity at 3 months (beta: -0.002; 95% confidence interval [CI]: -0.004 to -0.001) and after 4 months of MTX use (beta: -0.003; 95% CI: -0.005 to -0.002). Similarly, higher MTX-PG correlated with lower disease activity in psoriasis (R: -0.82; 95% CI: -0.976 to -0.102). Higher MTX-PG was observed in RA, JIA and psoriasis responders (mean difference: 5.2 nmol/L MTX-PG(total); P < .01). ConclusionWe showed that higher concentrations of erythrocyte MTX-PG were associated with lower disease activity in RA, JIA and psoriasis. These findings are an important step towards implementation of TDM for MTX treatment across IMIDs.

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