Evidence map›Paper›PMID 41075036›Full record

ReviewMetabolic brain disease2025

Gut microbiota reconstitution and control of α-synucleinopathy with β-glucans: a promising approach for individuals with parkinson's disease.

Faezeh Hatami, Zahra Aghelan, Mahan Rezaie Pouya, Melina Moulaeian, Ali Rastegari, Seyed Hosien Abtahi, Shaghayegh Hoseini

Abstract readReview
PubMed Publisher
In one paragraph

Review in Metabolic brain disease, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Review
  2. Review
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

7 authors.

Faezeh HatamiStudent Research Committee, TeMS.C., Islamic Azad University, Tehran, Iran.
Zahra AghelanDepartment of Clinical Biochemistry, TeMS.C., Islamic Azad University, Tehran, Iran. zahraaghelan@iau.ac.ir.ORCID 0000-0001-8375-7647
Mahan Rezaie PouyaStudent Research Committee, TeMS.C., Islamic Azad University, Tehran, Iran.
Melina MoulaeianStudent Research Committee, TeMS.C., Islamic Azad University, Tehran, Iran.
Ali RastegariYoung Researchers and Elite Club, TeMS.C., Islamic Azad University, Tehran, Iran.
Seyed Hosien AbtahiDepartment of Laboratory Hematology and Blood Banking, Faculty of Medicine, Tarbiat Modares University, Tehran, Iran.
Shaghayegh HoseiniStudent Research Committee, TeMS.C., Islamic Azad University, Tehran, Iran.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Parkinson's disease (PD) ranks as the second most prevalent neurodegenerative condition affecting individuals in their middle age and beyond. Its hallmark features include the abnormal accumulation of α-synuclein protein and the progressive loss of dopaminergic neurons. A substantial body of evidence supports the notion that an imbalance in the gut microbiome, known as dysbiosis, contributes to the misfolding and accumulation of α-synuclein, a key pathological feature of PD. This finding raises the possibility that restoring the gut microbiome, particularly the bacteria associated with α-synuclein, could serve as a promising therapeutic approach for PD. There is evidence that β-glucan can play an important role in the reconstitution of gut microbiome. In this regard, this study reviews the evidence showing the role of β-glucan in reducing α-synuclein accumulation and mitigating the progression of PD. This scooping review study presents promising prospects for advancing novel therapeutic approaches to benefit individuals with PD.

Indexed as

alpha-Synucleinbeta-GlucansGastrointestinal MicrobiomeParkinson DiseaseSynucleinopathiesAnimalsDysbiosisHumansalpha-Synucleinbeta-GlucansGut microbiotaParkinson's diseaseΑ-synucleinΒ- glucan

Identifiers

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.