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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 |
Files for this record:
| File | Description | Size | Format | |
|---|---|---|---|---|
| gpb_20_2_274.pdf | 2,45 MB | Adobe PDF | View/Open |
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