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A cross-sectional study of MRI features and the gut microbiome in pediatric-onset multiple sclerosis

  • Feng Zhu
  • , Yinshan Zhao
  • , Douglas L. Arnold
  • , Amit Bar-Or
  • , Charles N. Bernstein
  • , Christine Bonner
  • , Morag Graham
  • , Janace Hart
  • , Natalie Knox
  • , Ruth Ann Marrie
  • , Ali I. Mirza
  • , Julia O'Mahony
  • , Gary Van Domselaar
  • , E. Ann Yeh
  • , Brenda Banwell
  • , Emmanuelle Waubant
  • , Helen Tremlett

Research output: Contribution to journal › Article › peer-review

Abstract

Objective: To identify gut microbiome features associated with MRI lesion burden in persons with pediatric-onset multiple sclerosis (symptom onset <18 years). Methods: A cross-sectional study involving the Canadian Paediatric Demyelinating Disease Network study participants. Gut microbiome features (alpha diversity, phylum- and genus-level taxa) were derived using 16S rRNA sequencing from stool samples. T1- and T2-weighted lesion volumes were measured on brain MRI obtained within 6 months of stool sample procurement. Associations between the gut microbiota and MRI metrics (cube-root-transformed) were assessed using standard and Lasso regression models. Results: Thirty-four participants were included; mean ages at symptom onset and MRI were 15.1 and 19.0 years, respectively, and 79% were female. The T1- and T2-weighted lesion volumes were not significantly associated with alpha diversity (age and sex-adjusted p > 0.08). At the phylum level, high Tenericutes (relative abundance) was associated with higher T1 and T2 volumes (β coefficient = 0.25, 0.37) and high Firmicutes, Patescibacteria or Actinobacteria with lower lesion volumes (β coefficient = −0.30 to −0.07). At the genus level, high Ruminiclostridium, whereas low Coprococcus 3 and low Erysipelatoclostridium were associated with higher lesion volumes. Interpretation: Our study characterized the gut microbiota features associated with MRI lesion burden in pediatric-onset MS, shedding light onto possible pathophysiological mechanisms.

Original languageEnglish (US)
Pages (from-to)486-496
Number of pages11
JournalAnnals of Clinical and Translational Neurology
Volume11
Issue number2
DOIs
StatePublished - Feb 2024
Externally publishedYes

ASJC Scopus subject areas

  • General Neuroscience
  • Clinical Neurology

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