Fecal microbiota in children with juvenile idiopathic arthritis treated with methotrexate or etanercept

Anders Öman1, Johan Dicksved2, Lars Engstrand3

  • 1Department of Women's and Children's Health, Uppsala University, Uppsala, Sweden. anders.oman@kbh.uu.se.

Abstract

Insights

Standard juvenile idiopathic arthritis (JIA) treatments, methotrexate and etanercept, showed minor, non-significant changes in fecal microbiota composition and short-chain fatty acids (SCFAs) in children. These findings suggest treatment effects on the gut microbiome are not directly linked to therapeutic outcomes.

Area of Science:

  • Microbiome research
  • Pediatric rheumatology
  • Gastroenterology

Background:

  • Altered fecal microbiota is observed in children with juvenile idiopathic arthritis (JIA).
  • The impact of standard JIA treatments on the gut microbiome remains unclear.
  • Key treatments include methotrexate and anti-tumor necrosis factor alpha agents like etanercept.

Purpose of the Study:

  • To investigate the effects of methotrexate and etanercept on fecal microbiota composition and function in children with JIA.
  • To analyze changes in fecal short-chain fatty acids (SCFAs) during treatment.

Main Methods:

  • Compared fecal microbiota in treatment-naïve, methotrexate-treated, and etanercept-treated children with JIA.
  • Utilized 16S rRNA gene sequencing for microbiota analysis.
  • Analyzed fecal SCFAs using high-performance liquid chromatography in paired samples.

Main Results:

  • No significant differences in overall microbiota diversity or composition were found between treatment groups.
  • Minor, non-significant changes in community composition and taxa relative abundance were observed in paired samples.
  • Fecal SCFA levels did not significantly differ before and during treatment.

Conclusions:

  • Methotrexate and etanercept treatments induced minor, non-significant alterations in the fecal microbiota and SCFAs.
  • These observed changes are unlikely to be directly related to the therapeutic mechanisms of methotrexate or etanercept in JIA.

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