Abstract

Inside cells, the immunomodulator methotrexate (MTX) undergoes the addition of glutamates to form methotrexate polyglutamates (MTX-Glu)—promising biomarkers of systemic exposure and treatment response to MTX in rheumatology. MTX-Glu are underexplored in Inflammatory Bowel Disease (IBD), with no data in pediatrics. In this cross-sectional secondary analysis, we assessed the relationships between MTX-Glu and MTX dose and treatment response in pediatric IBD. Twenty-one children with IBD, receiving maintenance therapy with infliximab (IFX) and MTX, had MTX-Glu1–6 concentrations and IFX troughs/antibodies measured and disease activity assessed for comparison in remission vs. active IBD using non-parametric tests, with associations explored using Spearman’s correlation (ρ) and regression analyses; SASv9.4 (α = 0.05). Total and long-chain MTX-Glu correlated with MTX dose (ρ = 0.51 and 0.56, respectively; p ≤ 0.02). In children with Crohn’s disease (n = 19), short-chain MTX-Glu1–2 were 2.5-fold higher in remission vs. active disease, approaching statistical significance (p = 0.066), with no statistical differences in IFX trough (p = 0.549) between groups. Our study highlights a potential role for long-chain MTX-Glu in the therapeutic drug monitoring of MTX in IBD. It is the first study in pediatric IBD and, although statistical significance was not reached, our findings also suggest that higher short-chain MTX-Glu levels may be associated with IBD treatment response to MTX in children.

Highlights

  • Methotrexate (MTX) is a folic acid analog used as monotherapy, or in combination with anti-TNF-α agents, for the treatment of autoimmune disorders [1]

  • To the best of our knowledge, this is the first study of MTX-Glun levels in pediatric

  • Our data demonstrate that long-chain MTX-Glun levels correlate with methotrexate dose and could, serve as markers of systemic MTX exposure, offering a therapeutic drug monitoring option for MTX

Read more

Summary

Introduction

Methotrexate (MTX) is a folic acid analog used as monotherapy, or in combination with anti-TNF-α agents, for the treatment of autoimmune disorders [1]. MTX enters cells via folate transporters and receptors, and undergoes the addition of glutamic acid (Glu) residues by folylpolyglutamate synthetase to form methotrexate polyglutamates (MTX-Glun ) [2], where n represents the number of glutamic acid residues, with MTX-Glu denoting the parent form of MTX. The polyglutamated metabolites of MTX have a differential activity profile compared to the parent drug, with similar inhibitory activity against dihydrofolate reductase, but increased direct inhibitory activity against folate-dependent enzymes involved in purine. Pharmaceuticals 2021, 14, 463 and pyrimidine biosynthesis [4]. Erythrocyte concentrations of MTX-Glun have been associated with systemic exposure to MTX and MTX treatment efficacy [3,5,6,7]

Methods
Results
Conclusion
Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call