Evidence map›Paper›PMID 42206189›Full record

ArticleFrontiers in microbiomes2026

Identifying microbial biomarkers of neurodegeneration: a comparative study in Alzheimer's and Parkinson's disease.

Simon De Jaegher, David Pinzauti, Maria D'Aguanno, Erika Parkinson, James Schofield, Fabio Strazzeri, Paul Skipp, Rebekah Penrice-Randal, Amy Kunicki, Beth McCausland and 3 more

Abstract read
In one paragraph

Article in Frontiers in microbiomes, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

13 authors.

Simon De JaegherThe BioArte Ltd., Life Science Park, Triq San Giljan, San Gwann, Malta.
David PinzautiThe BioArte Ltd., Life Science Park, Triq San Giljan, San Gwann, Malta.
Maria D'AguannoThe BioArte Ltd., Life Science Park, Triq San Giljan, San Gwann, Malta.
Erika ParkinsonTopMD Precision Medicine Ltd, Southampton, United Kingdom.
James SchofieldTopMD Precision Medicine Ltd, Southampton, United Kingdom.
Fabio StrazzeriTopMD Precision Medicine Ltd, Southampton, United Kingdom.
Paul SkippTopMD Precision Medicine Ltd, Southampton, United Kingdom.
Rebekah Penrice-RandalTopMD Precision Medicine Ltd, Southampton, United Kingdom.
Amy KunickiClinical Neurosciences, Clinical and Experimental Sciences, Faculty of Medicine, University of Southampton, Southampton, United Kingdom.
Beth McCauslandClinical Neurosciences, Clinical and Experimental Sciences, Faculty of Medicine, University of Southampton, Southampton, United Kingdom.
Christopher KippsClinical Neurosciences, Clinical and Experimental Sciences, Faculty of Medicine, University of Southampton, Southampton, United Kingdom.
Jay AminClinical Neurosciences, Clinical and Experimental Sciences, Faculty of Medicine, University of Southampton, Southampton, United Kingdom.
Manuele BiazzoThe BioArte Ltd., Life Science Park, Triq San Giljan, San Gwann, Malta.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Neurodegenerative disorders such as Alzheimer's disease (AD) and Parkinson's disease (PD) have been increasingly linked to alterations of the gut microbiota, although reported microbial signatures remain heterogeneous and often lack taxonomic resolution. Methods: In the present study, we applied full-length 16S rRNA gene sequencing to characterize gut microbiota composition in 152 individuals, including patients with AD (n = 37), PD (n = 65), and age-matched healthy controls (n = 50), using a unified bioinformatic and statistical framework with adjustment for relevant demographic covariates. Results: Alzheimer's disease was associated with a modest but significant reduction in microbial richness and Shannon diversity compared with controls, whereas no alpha diversity differences were observed in PD. Beta diversity analyses revealed significant compositional differences across diagnostic groups, driven primarily by PD and modulated by sex but not age. Species-level differential abundance analysis identified a PD-associated microbial signature characterized by reduced abundances of short-chain fatty acid-producing bacteria, including Discussion: Overall, these findings indicate that Parkinson's disease is characterized by a targeted disruption of beneficial butyrate-producing bacteria, whereas Alzheimer's disease exhibits subtler and less consistent microbiome alterations. Our results underscore the importance of species-level resolution for identifying disease-associated microbial signatures.

Indexed as

Alzheimer’s diseasefull-length 16S rRNA gene sequencinggut microbiotaParkinson’s diseasespecies-level resolution

Identifiers

PMID42206189
PMCPMC13201170

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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.