Gut microbiota dysbiosis in Parkinson disease: A systematic review and pooled analysis

Sven Kleine Bardenhorst1, Emanuele Cereda2, Marco Severgnini3

  • 1Institute of Epidemiology and Social Medicine, University of Münster, Münster, Germany.

Abstract

Insights

Harmonizing gut microbiome studies in Parkinson disease (PD) reveals key bacterial taxa. Reduced butyrate producers and increased Akkermansia are characteristic of PD-associated microbiota, suggesting a role in disease pathogenesis.

Area of Science:

  • Neuroscience
  • Microbiology
  • Genetics

Background:

  • The gut microbiome's role in Parkinson disease (PD) pathogenesis is under investigation, but results are heterogeneous due to varying methodologies.
  • Discrepancies in PD research stem from diverse pathologies and inconsistent workflows from sampling to statistical analysis.

Purpose of the Study:

  • To harmonize workflows across studies to reduce methodological heterogeneity in gut microbiome research.
  • To perform a pooled analysis of gut microbiota in Parkinson disease (PD) to account for remaining sources of heterogeneity.

Main Methods:

  • Conducted a systematic review to identify studies comparing gut microbiota in PD patients and healthy controls.
  • Developed a harmonized workflow for bioinformatics processing and statistical analysis.
  • Utilized Bayesian random-effects meta-analysis on individual patient-level data.

Main Results:

  • Harmonized workflows minimized statistical method differences, identifying a core set of PD-associated bacterial taxa.
  • Increased abundance of Akkermansia and Bifidobacterium genera were observed in PD patients.
  • Decreased abundance of Roseburia and Faecalibacterium genera were characteristic of PD-associated microbiota.

Conclusions:

  • Reduced levels of butyrate-producing taxa may contribute to intestinal inflammation and gut barrier dysfunction in PD.
  • Akkermansia may degrade the mucus layer, potentially increasing gut permeability in Parkinson disease (PD).
  • Translocation of pathogenic metabolites through a compromised gut barrier may influence the enteric nervous system in PD.

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