Evidence map›Paper›PMID 40824914›Full record

ArticlePloS one2025

Microbial diversity in drug-naïve Parkinson's disease patients.

Eliša Papić, Valentino Rački, Mario Hero, Ana Nyasha Zimani, Mojca Čižek Sajko, Gloria Rožmarić, Nada Starčević Čizmarević, Saša Ostojić, Miljenko Kapović, Goran Hauser and 4 more

Abstract read
In one paragraph

Article in PloS one, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Review
  2. Review
  3. Article
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

14 authors.

Eliša PapićDepartment of Neurology, Faculty of Medicine, University of Rijeka, Rijeka, Croatia.
Valentino RačkiDepartment of Neurology, Faculty of Medicine, University of Rijeka, Rijeka, Croatia.
Mario HeroDepartment of Neurology, Faculty of Medicine, University of Rijeka, Rijeka, Croatia.ORCID https://orcid.org/0000-0003-0933-3760
Ana Nyasha ZimaniClinical Institute of Genomic Medicine, University Medical Centre Ljubljana, Slovenia.
Mojca Čižek SajkoClinical Institute of Genomic Medicine, University Medical Centre Ljubljana, Slovenia.ORCID https://orcid.org/0000-0001-8859-1199
Gloria RožmarićDepartment of Neurology, Faculty of Medicine, University of Rijeka, Rijeka, Croatia.ORCID https://orcid.org/0000-0002-5086-5403
Nada Starčević ČizmarevićDepartment of Medical Biology and Genetics, Faculty of Medicine, University of Rijeka, Rijeka, Croatia.
Saša OstojićDepartment of Medical Biology and Genetics, Faculty of Medicine, University of Rijeka, Rijeka, Croatia.
Miljenko KapovićDepartment of Medical Biology and Genetics, Faculty of Medicine, University of Rijeka, Rijeka, Croatia.
Goran HauserDepartment of Internal Medicine, Faculty of Medicine, University of Rijeka, Rijeka, Croatia.
Aleš MaverClinical Institute of Genomic Medicine, University Medical Centre Ljubljana, Slovenia.
Borut PeterlinClinical Institute of Genomic Medicine, University Medical Centre Ljubljana, Slovenia.
Anja KovandaClinical Institute of Genomic Medicine, University Medical Centre Ljubljana, Slovenia.ORCID https://orcid.org/0000-0002-7468-878X
Vladimira VuletićDepartment of Neurology, Faculty of Medicine, University of Rijeka, Rijeka, Croatia.ORCID https://orcid.org/0000-0002-7857-857X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Parkinson's disease (PD) is a neurological disorder characterized by rigidity, bradykinesia and tremor. Several genetic and environmental causes of PD are known, and there is emerging evidence of the possible contribution of the gut microbiome to the disease onset, severity, and response to therapy. While previous research has shown several differences in the microbiome of PD patients under therapy as opposed to healthy controls, few prospective studies have included drug-naïve patients. In order to evaluate the gut microbiome composition prior to therapy initiation, we collected and performed 16S rRNA gene sequencing of the stool samples from 49 drug-naïve PD patients and compared them to 34 diet and lifestyle-matched controls from the Croatian population (GiOPARK Project). While no significant alpha diversity difference was observed between the patients and controls, the differential relative abundance analysis showed an increase in Bacteroides fluxus, B. interstinalis, B. eggerthii, and Dielma fastidiosa in the drug-naïve PD patients compared to controls, while Alistipes, Barnesiella and Dialister spp. were decreased in patients compared to controls. Despite preserved overall diversity, these changes may indicate early microbial dysbiosis and represent a foundation for future studies exploring microbiome changes across disease progression and treatment.

Indexed as

Gastrointestinal MicrobiomeParkinson DiseaseAgedBacteriaCase-Control StudiesDysbiosisFecesFemaleHumansMaleMiddle AgedRNA, Ribosomal, 16SRNA, Ribosomal, 16S

Identifiers

PMID40824914
PMCPMC12360607

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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.