Gut microbiota linked to hydrocephalus through inflammatory factors: a Mendelian randomization study

Yingjie Shen1, Changyu Li2, Xi Zhang1

  • 1Department of Neurosurgery, National Health Commission Key Laboratory of Cell Transplantation, The First Affiliated Hospital of Harbin Medical University, Harbin, Heilongjiang, China.

PubMed
Abstract

Insights

The gut microbiota influences hydrocephalus risk. Certain bacteria, like Firmicutes, may reduce obstructive hydrocephalus risk by modulating IL-17A levels, while others impact normal-pressure hydrocephalus via IL-27.

Area of Science:

  • Microbiome research
  • Neurology
  • Immunology

Background:

  • The gut microbiota's role in neurological disorders is increasingly recognized.
  • Specific mechanisms linking gut bacteria to hydrocephalus remain largely unexplored.
  • Inflammatory factors may mediate the gut microbiota-hydrocephalus axis.

Purpose of the Study:

  • To investigate the causal relationship between gut microbiota composition and hydrocephalus.
  • To identify the mediating role of inflammatory factors, specifically IL-17A and IL-27, in this relationship.
  • To elucidate potential mechanistic pathways between the gut microbiota and hydrocephalus.

Main Methods:

  • Mendelian randomization (MR) analyses utilizing summary statistics.
  • Assessment of causal links between gut microbiota taxa, IL-17A, IL-27, and hydrocephalus types.
  • Mediator MR analyses to quantify the indirect effects of gut microbiota on hydrocephalus via inflammatory factors.
  • Sensitivity analyses to ensure result robustness.

Main Results:

  • The phylum Firmicutes was associated with a reduced risk of obstructive hydrocephalus (OR, 0.34; P=2.71E-03).
  • Firmicutes decreased obstructive hydrocephalus risk by increasing IL-17A levels (mediating effect = 21.01%).
  • The genus Eubacterium ruminantium group increased normal-pressure hydrocephalus risk by decreasing IL-27 levels (mediating effect = 7.48%).

Conclusions:

  • Gut microbiota composition is causally linked to hydrocephalus risk.
  • Inflammatory factors IL-17A and IL-27 mediate the relationship between specific gut bacteria and hydrocephalus.
  • These findings provide a foundation for understanding the gut microbiota-brain axis in hydrocephalus pathogenesis.