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Abstract Details

Implications of Gut Microbiome Dysbiosis in Parkinson's Disease: A Literature Review.
Movement Disorders
P14 - Poster Session 14 (8:00 AM-9:00 AM)
3-004

To review the evidence showing an association between gut microbiome (GM) dysbiosis and Parkinson's disease (PD), with an emphasis on the mechanisms by which GM dysbiosis may be involved in PD pathophysiology.

The GM plays an important role in the development and homeostasis of different body systems, including the central nervous system (CNS) via the gut-brain axis. Autopsy-based studies have demonstrated that α-synucleinopathy is not limited to the CNS but also affects the enteric nervous system (ENS) of PD patients. Moreover, gastrointestinal symptoms of PD predate motor symptoms. Accordingly, studies have looked at GM changes in PD, the consequences of these changes and their possible implications in PD pathophysiology. 

A literature review was conducted using PubMed to identify studies that evaluated the differences between GM of PD patients and of healthy individuals. Also, studies that investigated the mechanisms by which GM changes might trigger or influence PD pathogenesis were reviewed.

There are significant changes in GM of PD patients as compared to that of healthy individuals, which cause decreased production of neuroprotective factors such as short-chain fatty acids (SCFA) and ghrelin. Such changes also increase the release of bacterial neurotoxins including lipopolysaccharide, epoxomicin, and β-N-methylamino-L-alanine into the systemic circulation which might potentiate nigral dopaminergic degeneration given the disrupted blood-brain barrier in PD.

GM changes might be related to the underlying pathophysiology of PD via different mechanisms. A better understanding of the consequences of GM changes, especially those taking place in the ENS and CNS, can help identify the key factors triggering α-synucleinopathy, and provide potential targets for clinical trials to test potential disease-modifying agents for PD including SCFA, probiotics, Tumor Necrosis Factor-alpha antagonists and recombinant ghrelin.

Authors/Disclosures
Mohamed Elfil, MBBCh
PRESENTER
Dr. Elfil has nothing to disclose.
No disclosure on file
Mohamed I. Kandil, MD No disclosure on file
Nada Ahmed, MD (Prisma Health) Dr. Ahmed has nothing to disclose.
Sara M. Schaefer, MD, FÂé¶¹´«Ã½Ó³»­ Dr. Schaefer has received personal compensation in the range of $500-$4,999 for serving as an Editor, Associate Editor, or Editorial Advisory Board Member for Movement Disorders Journal. The institution of Dr. Schaefer has received research support from American Parkinson Disease Association. Dr. Schaefer has received personal compensation in the range of $500-$4,999 for serving as a RITE Section Lead with Âé¶¹´«Ã½Ó³»­. Dr. Schaefer has received personal compensation in the range of $500-$4,999 for serving as a QOD Question Writer with Âé¶¹´«Ã½Ó³»­.
Brian Koo, MD Dr. Koo has received personal compensation in the range of $500-$4,999 for serving as a Consultant for American Regent. Dr. Koo has received personal compensation in the range of $5,000-$9,999 for serving as an Expert Witness for Speckhals Law. The institution of Dr. Koo has received research support from Department of Defense.