Methotrexate Triglutamate as a Determinant of Clinical Response in Mexican Patients With Rheumatoid Arthritis: Pharmacokinetics and Dose Recommendation
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Methotrexate is the gold standard treatment in rheumatoid arthritis. Once absorbed, it is internalized in cells, where glutamate residues are added to produce polyglutamated forms, which are responsible for the effect of methotrexate. The aim of the current study is to determine the relationship between methotrexate triglutamate concentrations and the clinical evolution in rheumatoid arthritis patients, as well as to characterize the variability in both features to propose strategies for low-dose methotrexate optimization. The quantification of methotrexate triglutamate concentration in red blood cells was performed through ultra-performance liquid chromatography coupled with mass spectrometry. Polymorphisms of genes involved in the formation of polyglutamates were determined by real-time polymerase chain reaction. A multivariate regression was performed to determine the covariates involved in the variability of methotrexate triglutamate concentrations and a population pharmacokinetics model was developed through nonlinear mixed-effects modeling. Disease activity score changed according to methotrexate triglutamate concentrations; patients with good response to treatment had higher concentrations than moderate or nonresponding patients. The methotrexate triglutamate concentrations were related to time under treatment, dose, red blood cells, and body mass index. A 1-compartment open model was selected to estimate the pharmacokinetic parameters; the typical total clearance (L/day) was determined as 1.45 * (body mass index/28 kg/m2) * (red blood cells/4.6 × 106 cells/μL) and the volume of distribution was 52.4 L, with an absorption rate of 0.0346/day and a fraction metabolized of 1.03%25. Through the application of the model, the initial dose of methotrexate is proposed on the basis of stochastic simulations and considering methotrexate triglutamate concentrations found in responders patients. © 2021, The American College of Clinical Pharmacology
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body mass index; low-dose methotrexate; pharmacokinetics of methotrexate triglutamate; polyglutamates of methotrexate; rheumatoid arthritis; UPLC/MS/MS alanine aminotransferase; aspartate aminotransferase; biological marker; disease modifying antirheumatic drug; genomic DNA; glutamic acid; methotrexate; methotrexate triglutamate; polyglutamic acid; unclassified drug; antirheumatic agent; methotrexate; methotrexate polyglutamate; polyglutamic acid; anemia; Article; body mass; DAS28; diarrhea; drug blood level; drug formulation; erythrocyte; erythrocyte sedimentation rate; gastritis; genotype; human; hypertransaminasemia; inflammation; leukopenia; longitudinal study; low drug dose; maintenance drug dose; major clinical study; mass spectrometry; Mexican; multivariate analysis; nausea; observational study; prospective study; real time polymerase chain reaction; recommended drug dose; regression analysis; remission; rheumatoid arthritis; rheumatologist; simulation; treatment response; ultra performance liquid chromatography; validation study; age; biological model; blood; body weight; dose response; metabolic clearance rate; Mexico; rheumatoid arthritis; single nucleotide polymorphism; Age Factors; Antirheumatic Agents; Arthritis, Rheumatoid; Body Mass Index; Body Weight; Dose-Response Relationship, Drug; Erythrocytes; Genotype; Humans; Longitudinal Studies; Metabolic Clearance Rate; Methotrexate; Mexico; Models, Biological; Polyglutamic Acid; Polymorphism, Single Nucleotide; Prospective Studies; Real-Time Polymerase Chain Reaction
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