Disease-modifying therapy for multiple sclerosis: Implications for gut microbiota

Silvy Pilotto1, Magdalena Zoledziewska2, Giuseppe Fenu3

  • 1Multiple Sclerosis Center, ASL Cagliari, Department of Medical Sciences and Public Health, Binaghi Hospital, University of Cagliari, via Is Guadazzonis 2, Cagliari 09126, Italy.

Abstract

Insights

Disease-modifying therapies (DMTs) for multiple sclerosis (MS) impact the gut microbiome. While studies show microbial changes, the direct association and consistency require further investigation for prognostic implications.

Area of Science:

  • Neuroimmunology
  • Microbiome Research
  • Pharmacology

Background:

  • Gut microbiota plays a role in multiple sclerosis (MS) pathophysiology.
  • Disease-modifying therapies (DMTs) for MS influence the gut microenvironment and immune system.
  • Understanding the impact of DMTs on the gut microbiome is crucial for MS management.

Purpose of the Study:

  • To review and summarize the current literature on the effects of DMTs on the gut microbiome in MS patients.
  • To explore the implications of these changes for MS pathophysiology and treatment.

Main Methods:

  • A comprehensive literature search was conducted on PubMed using keywords related to MS, gut microbiome, and DMTs.
  • Original research articles in English were included in this narrative review.
  • Studies focused on first-line DMTs (dimethyl fumarate, glatiramer acetate, interferon β 1b) and other treatments (natalizumab, fingolimod, anti-CD20).

Main Results:

  • Ten eligible studies were identified, comprising seven case-control and three cohort studies.
  • Changes in the gut microbiome were observed in patients exposed to DMTs.
  • The association between DMT exposure and microbial alterations was often indirect.

Conclusions:

  • Emerging evidence suggests DMTs alter the gut microbiome in MS patients.
  • Current findings on the specific microbial changes and their direct association with DMTs are inconsistent.
  • Future research needs to mitigate methodological bias to identify a "microbial signature" for MS and DMT roles.

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