Please use this identifier to cite or link to this item: doi:10.22028/D291-47588
Title: Effects of Resistant Starch on Symptoms, Fecal Markers, and Gut Microbiota in Parkinson's Disease - The RESISTA-PD Trial
Author(s): Becker, Anouck
Schmartz, Georges Pierre
Gröger, Laura
Grammes, Nadja
Galata, Valentina
Philippeit, Hannah
Weiland, Jacqueline
Ludwig, Nicole
Meese, Eckart
Tierling, Sascha
Walter, Jörn
Schwiertz, Andreas
Spiegel, Jörg
Wagenpfeil, Gudrun
Faßbender, Klaus
Keller, Andreas
Unger, Marcus M.
Language: English
Title: Genomics Proteomics Bioinformatics
Volume: 20 (2022)
Issue: 2
Pages: 274-287
Publisher/Platform: Elsevier
Year of Publication: 2021
Free key words: Parkinson’s disease
Short-chain fatty acid
Microbiota
Metagenomics
Intestinal inflammation
DDC notations: 500 Science
610 Medicine and health
Publikation type: Journal Article
Abstract: The composition of the gut microbiota is linked to multiple diseases, including Parkin son’s disease (PD). Abundance of bacteria producing short-chain fatty acids (SCFAs) and fecal SCFA concentrations are reduced in PD. SCFAs exert various beneficial functions in humans. In the interventional, monocentric, open-label clinical trial ‘‘Effects of Resistant Starch on Bowel Habits, Short Chain Fatty Acids and Gut Microbiota in Parkinson’s Disease” (RESISTA-PD; ID: NCT02784145), we aimed at altering fecal SCFAs by an 8-week prebiotic intervention with resistant starch (RS). We enrolled 87 subjects in three study-arms: 32 PD patients received RS (PD +RS),30control subjects received RS, and 25 PD patients received solely dietary instructions. We performed paired-end 100 bp length metagenomic sequencing of fecal samples using the BGISEQ platform at an average of 9.9 GB. RS was well-tolerated. In the PD + RS group, fecal butyrate concentrations increased significantly, and fecal calprotectin concentrations dropped significantly after 8 weeks of RS intervention. Clinically, we observed a reduction in non-motor symptomloadinthePD+RSgroup.Thereference-basedanalysisofmetagenomeshighlightedstable alpha-diversity and beta-diversity across the three groups, including bacteria producing SCFAs. Reference-free analysis suggested punctual, yet pronounced differences in the metagenomic signature in the PD + RS group. RESISTA-PD highlights that a prebiotic treatment with RS is safe and well-tolerated in PD. The stable alpha-diversity and beta-diversity alongside altered fecal butyrate and calprotectin concentrations call for long-term studies, also investigating whether RS is able to modify the clinical course of PD.
DOI of the first publication: 10.1016/j.gpb.2021.08.009
URL of the first publication: https://doi.org/10.1016/j.gpb.2021.08.009
Link to this record: urn:nbn:de:bsz:291--ds-475882
hdl:20.500.11880/41610
http://dx.doi.org/10.22028/D291-47588
ISSN: 2210-3244
1672-0229
Date of registration: 28-Apr-2026
Faculty: M - Medizinische Fakultät
NT - Naturwissenschaftlich- Technische Fakultät
Department: M - Humangenetik
M - Medizinische Biometrie, Epidemiologie und medizinische Informatik
M - Neurologie und Psychiatrie
NT - Biowissenschaften
Professorship: M - Prof. Dr. Klaus Faßbender
M - Univ.-Prof. Dr. Andreas Keller
M - Prof. Dr. Eckart Meese
NT - Prof. Dr. Jörn Walter
Collections:SciDok - Der Wissenschaftsserver der Universität des Saarlandes

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