PreprintCited by 102Gut microbiota and healthParkinson's Disease Mechanisms and TreatmentsGastrointestinal motility and disorders

Effects of Resistant Starch on Symptoms, Fecal Markers and Gut Microbiota in Parkinson’s Disease – The RESISTA-PD Trial

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Becker, Anouck, Schmartz, Georges Pierre, Gröger, Laura, Grammes, Nadja, Galata, Valentina, Philippeit, Hannah, Weiland, Jacqueline, Ludwig, Nicole +9 more·2021·Genomics Proteomics & Bioinformatics

Preprint — published as 10.1016/j.gpb.2021.08.009 · Paper page

Abstract

The composition of the gut microbiome is linked to multiple diseases, including Parkinson’s disease (PD). 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 RESISTA-PD ( 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 receiving RS (PD + RS), 30 control subjects receiving RS, and 25 PD patients receiving solely dietary instructions. We performed paired-end 100 base pair length metagenomic sequencing of fecal samples using the BGISEQ platform at an average of 9.9 GB. RS was well-tolerated. In PD + RS, fecal butyrate concentrations increased significantly and fecal calprotectin concentrations dropped significantly after 8 weeks of RS. Clinically, we observed a reduction in non-motor symptoms load in PD + RS. The reference-based analysis of metagenomes highlighted stable 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 PD + RS. 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 calls for long-term studies, also investigating whether RS is able to modify the clinical course of PD.

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References 59 · Cited by 102

Authors
Becker, A., Schmartz, G. P., Gröger, L., Grammes, N., Galata, V., Philippeit, H., Weiland, J., Ludwig, N., Meese, E., Tierling, S., Walter, J., Schwiertz, A., Spiegel, J., Wagenpfeil, G., Faßbender, K., Keller, A., & Unger, M. M.
Affiliations
  • Saarland University (DE)
  • Institut für Mikroökologie (DE)
Corresponding author
Unger, Marcus M.
Venue
Genomics Proteomics & Bioinformatics
Publisher
openRxiv
Published
2021-02-08
Volume
20
Issue
2
Pages
274-287
ISSN
1672-0229 (ISSN-L)
OpenAlex
W3214815292
Cited by
102
References
59
Citations by year
2026: 16 · 2025: 31 · 2024: 28 · 2023: 13 · 2022: 12 · 2021: 2
FWCI
4.32
Type
journal article
Language
en
Open access
Licence
cc-by
Locations
  • Genomics Proteomics & Bioinformatics (publishedVersion, cc-by)
  • medRxiv (acceptedVersion, cc-by-nc-nd)
  • PubMed Central (publishedVersion, cc-by)
  • PubMed (publishedVersion)
  • DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
  • Publications of the UdS (Saarland University) (cc-by)
Funders
Michael J. Fox Foundation for Parkinson's Research (14603)
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Gut microbiota and health
  • Health Sciences › Medicine › Neurology › Parkinson's Disease Mechanisms and Treatments
  • Health Sciences › Medicine › Gastroenterology › Gastrointestinal motility and disorders
Keywords
resistant starch, Parkinson's disease, gut microbiota, short-chain fatty acids, butyrate, calprotectin, non-motor symptoms, fecal microbiota, metagenomics, dietary intervention
MeSH terms
Gastrointestinal Microbiome, Resistant Starch, Bacteria, Butyrates, Fatty Acids, Volatile, Feces, Humans, Parkinson Disease, Biomarkers, Leukocyte L1 Antigen Complex, Prebiotics

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