Evidence map›Paper›PMID 40686474›Full record

Observational studyEuropean journal of neurology2025

Influence of the Gut Microbiota on Acute Ischemic Stroke Functional Outcomes at Three Months.

Miquel Lledós, Luís Prats-Sánchez, Elena Muiño, Natalia Cullell, Laia Llucià-Carol, Jara Cárcel-Márquez, Cristina Gallego-Fabrega, Jesús M Martín-Campos, Rebeca Marín, Ana Aguilera-Simón and 6 more

Registry-linked trialAbstract readObservational Study
In one paragraph

Observational study in European journal of neurology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT04795687 (Association of Metagenomics and Transcriptomics With the Appearance and Evolution of an Ischemic Stroke), which is not on this map. Cited by 4 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed, 1 pooled it
–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.

NCT04795687 unknown statusnot on this map

Association of Metagenomics and Transcriptomics With the Appearance and Evolution of an Ischemic Stroke

TypeobservationalSponsorFundació Institut de Recerca de l'Hospital de la Santa Creu i Sant PauRan2020 to 2022Enrolled300ConditionsIschemic Stroke
3 · Its place in the literature

Who cites it

4 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. Article
  4. Observational
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

16 authors.

Miquel LledósStroke Pharmacogenomics and Genetics Laboratory, Institut de Recerca Sant Pau (IR SANT PAU), Barcelona, Spain.ORCID 0000-0001-8832-789X
Luís Prats-SánchezStroke Unit, Department of Neurology, Hospital de la Santa Creu i Sant Pau (HSCSP), Barcelona, Spain.ORCID 0000-0002-3192-4631
Elena MuiñoStroke Pharmacogenomics and Genetics Laboratory, Institut de Recerca Sant Pau (IR SANT PAU), Barcelona, Spain.
Natalia CullellStroke Pharmacogenomics and Genetics Laboratory, Institut de Recerca Sant Pau (IR SANT PAU), Barcelona, Spain.ORCID 0000-0001-5118-1014
Laia Llucià-CarolStroke Pharmacogenomics and Genetics Laboratory, Institut de Recerca Sant Pau (IR SANT PAU), Barcelona, Spain.
Jara Cárcel-MárquezStroke Pharmacogenomics and Genetics Laboratory, Institut de Recerca Sant Pau (IR SANT PAU), Barcelona, Spain.
Cristina Gallego-FabregaStroke Pharmacogenomics and Genetics Laboratory, Institut de Recerca Sant Pau (IR SANT PAU), Barcelona, Spain.
Jesús M Martín-CamposStroke Pharmacogenomics and Genetics Laboratory, Institut de Recerca Sant Pau (IR SANT PAU), Barcelona, Spain.
Rebeca MarínStroke Unit, Institut de Recerca Sant Pau (IR Sant Pau), Barcelona, Spain.
Ana Aguilera-SimónStroke Unit, Institut de Recerca Sant Pau (IR Sant Pau), Barcelona, Spain.ORCID 0000-0003-1428-8212
Marina Guasch-JiménezStroke Unit, Department of Neurology, Hospital de la Santa Creu i Sant Pau (HSCSP), Barcelona, Spain.
Garbiñe Ezcurra-DíazStroke Unit, Department of Neurology, Hospital de la Santa Creu i Sant Pau (HSCSP), Barcelona, Spain.ORCID 0000-0002-9511-3117
Pol Camps-RenomStroke Unit, Department of Neurology, Hospital de la Santa Creu i Sant Pau (HSCSP), Barcelona, Spain.ORCID 0000-0001-6587-6271
María Del Mar FreijoNeurology Service, Hospital Universitario de Cruces, Biocruces Bizkaia Health Research Institute, Barakaldo, Spain.
Joan Martí-FàbregasStroke Unit, Department of Neurology, Hospital de la Santa Creu i Sant Pau (HSCSP), Barcelona, Spain.ORCID 0000-0001-9229-8649
Israel Fernández-CadenasStroke Pharmacogenomics and Genetics Laboratory, Institut de Recerca Sant Pau (IR SANT PAU), Barcelona, Spain.

Funding

ERA-Net NEURON AC19/00106Instituto de Salud Carlos III CD20/00043Instituto de Salud Carlos III FI19/00309Instituto de Salud Carlos III PI18/01338Instituto de Salud Carlos III PI20/00925RICORS-ICTUS RD21/0006/0006
6 · The paper itself

Abstract

backgroundFunctional recovery from ischemic stroke (IS), the main cause of adult disability worldwide, is influenced by many factors, and a portion of interindividual variability remains unexplained.

methodsObservational study in a tertiary stroke centre of patients with IS analyzed using shotgun metagenomic sequencing (January 2020-March 2022). Functional outcomes were assessed according to modified Rankin Scale (mRS) scores 3-months post-IS, considering 0-2 favorable and 3-6 unfavorable. The causal relationship between several bacteria and post-IS outcomes was explored via two-sample Mendelian randomization (MR) analyses using Genome-Wide Association Analysis (GWAS) summary statistics.

resultsComparing 128 patients with favorable and unfavorable post-IS functional outcomes, β-diversity analysis showed a separation in microbial structure, and α-diversity measures revealed greater bacterial richness in the favorable outcomes group. Taxonomic profiling of the samples showed that a greater abundance of pathogenic bacteria (e.g., Pseudomonas, Finegoldia, Porphyromonas) was associated with an unfavorable outcome. Functional profiling of the samples revealed differences in the ethylbenzene degradation pathway and in 16S rRNA (uracil1498-N3)-methyltransferase. MR confirmed increased pyruvate levels to be causally associated with post-IS favorable outcomes (β = -0.50, 95% CI: -0.91, -0.10).

conclusionsOur study points to gut microbiota differences in patients with unfavorable versus favorable 3-month post-IS outcomes. Patients with unfavorable outcomes presented gut microbiota dysbiosis and alterations in multiple metabolic pathways.

trial registrationThis study was registered on 3 October 2021 with https://clinicaltrials.gov. Access number: NCT04795687.

Indexed as

Gastrointestinal MicrobiomeIschemic StrokeRecovery of FunctionAgedFemaleGenome-Wide Association StudyHumansMaleMiddle Agedfunctional outcomegut‐brain axisischemic strokemicrobiotashotgun metagenomics

Identifiers

PMID40686474
PMCPMC12278021

What OpenQuestion holds

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LicenceCC BY-NC-ND
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Registered trials

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.