Gut microbiota differences between healthy older adults and individuals with Parkinson's disease: A systematic review

  • Nathan D. Nuzum
  • , Amy Loughman
  • , Ewa A. Szymlek-Gay
  • , Ashlee Hendy
  • , Wei Peng Teo
  • , Helen Macpherson

Research output: Contribution to journalReview articlepeer-review

Abstract

The ‘Dual Hit’ hypothesis, stating that Parkinson's disease (PD) begins via olfactory pathways and the gut, and the gastrointestinal symptoms PD individuals face, have largely driven the interest of the gut's involvement in PD. Studies have since observed gut microbiota differences between PD groups and controls, with these alterations potentially relating to PD pathophysiology. However, differences in the studies’ methodologies precludes unanimity on the relationships of gut microbiota to PD. Thirteen observational case-control studies investigating gut microbiota in PD and controls were reviewed to assess how microbiota abundance and diversity relates to PD. Nine studies showed butyrate producing gut microbiota had lower abundances in PD compared to controls. Three studies reported α-diversity was higher, with one reporting it was lower, in PD compared to controls. Given most studies show abundance, not diversity, differences of butyrate producing bacteria between groups, we propose abundance differences are more associated with PD than microbiota diversity. As current research is observational, investigating how specific bacteria and their metabolites may alter throughout PD progression is warranted.

Original languageEnglish
Pages (from-to)227-241
Number of pages15
JournalNeuroscience and Biobehavioral Reviews
Volume112
DOIs
Publication statusPublished - May 2020
Externally publishedYes

Keywords

  • Alpha-diversity
  • Beta-diversity
  • Butyrate
  • Cognition
  • Microbiota-gut-brain axis
  • Motor-symptoms
  • Non-motor symptoms
  • Short chain fatty acid

Fingerprint

Dive into the research topics of 'Gut microbiota differences between healthy older adults and individuals with Parkinson's disease: A systematic review'. Together they form a unique fingerprint.

Cite this