Evidence map›Paper›PMID 40108151›Full record

ReviewNPJ Parkinson's disease2025

Comparative analysis of Parkinson's and inflammatory bowel disease gut microbiomes reveals shared butyrate-producing bacteria depletion.

Maeve E Krueger, Jake Sondag Boles, Zachary D Simon, Stephan D Alvarez, Nikolaus R McFarland, Michael S Okun, Ellen M Zimmermann, Christopher E Forsmark, Malú Gámez Tansey

Abstract readReview
In one paragraph

Review in NPJ Parkinson's disease, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

29 citing papers in PubMed.

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  19. Gut Microbiome as a Source of Probiotic Drugs for Parkinson's Disease.International journal of molecular sciences · 2025
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

Maeve E KruegerDepartment of Neuroscience, College of Medicine, University of Florida, Gainesville, FL, USA.ORCID http://orcid.org/0009-0004-6325-3678
Jake Sondag BolesDepartment of Neuroscience, College of Medicine, University of Florida, Gainesville, FL, USA.ORCID http://orcid.org/0000-0001-5501-2162
Zachary D SimonNorman Fixel Institute for Neurological Diseases, University of Florida, Gainesville, FL, USA.ORCID http://orcid.org/0000-0001-9297-2971
Stephan D AlvarezNorman Fixel Institute for Neurological Diseases, University of Florida, Gainesville, FL, USA.ORCID http://orcid.org/0009-0000-4420-7394
Nikolaus R McFarlandNorman Fixel Institute for Neurological Diseases, University of Florida, Gainesville, FL, USA.ORCID http://orcid.org/0000-0002-8699-8857
Michael S OkunNorman Fixel Institute for Neurological Diseases, University of Florida, Gainesville, FL, USA.ORCID http://orcid.org/0000-0002-6247-9358
Ellen M ZimmermannDepartment of Medicine, Division of Gastroenterology, College of Medicine, University of Florida, Gainesville, FL, USA.ORCID http://orcid.org/0000-0002-7966-2837
Christopher E ForsmarkDepartment of Medicine, Division of Gastroenterology, College of Medicine, University of Florida, Gainesville, FL, USA.ORCID http://orcid.org/0000-0002-2508-1543
Malú Gámez TanseyDepartment of Neuroscience, College of Medicine, University of Florida, Gainesville, FL, USA. mgtansey@ufl.edu.ORCID http://orcid.org/0000-0002-1719-4708

Funding

Parkinson's Foundation (Parkinson's Foundation, Inc.) PF-RCE-1945
6 · The paper itself

Abstract

Epidemiological studies reveal that inflammatory bowel disease (IBD) is associated with an increased risk of Parkinson's disease (PD). Gut dysbiosis has been documented in both PD and IBD, however it is currently unknown whether gut dysbiosis underlies the epidemiological association between both diseases. To identify shared and distinct features of the PD and IBD microbiome, we recruited 54 PD, 26 IBD, and 16 healthy control individuals and performed the first joint analysis of gut metagenomes. Larger, publicly available PD and IBD metagenomic datasets were also analyzed to validate and extend our findings. Depletions in short-chain fatty acid (SCFA)-producing bacteria, including Roseburia intestinalis, Faecalibacterium prausnitzii, Anaerostipes hadrus, and Eubacterium rectale, as well depletion in SCFA-synthesis pathways were detected across PD and IBD datasets, suggesting that depletion of these microbes in IBD may influence the risk for PD development.

Identifiers

PMID40108151
PMCPMC11923181

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.