Evidence map›Paper›PMID 42942992›Full record

ReviewNutrients2026

Gut Microbiome in Sporadic Cerebral Small Vessel Disease: MRI-Defined Phenotypes, Mechanistic Evidence, and Nutritional Implications for Brain Aging.

Tamas Jarecsny, Ferenc Fazekas, Nadim Al-Muhanna, Richard Schwab, Viktoria Hadnagy, Sara Laki, Janos Tamas Varga, Andrea Lehoczki, Virag Zabo, Diana Gorog and 1 more

Abstract readReview
In one paragraph

Review in Nutrients, 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

11 authors.

Tamas JarecsnyDepartment of Neurology and Stroke, Saint John's Central Hospital of North Buda, 1125 Budapest, Hungary.ORCID 0000-0002-8419-5292
Ferenc FazekasDepartment of Neurology and Stroke, Saint John's Central Hospital of North Buda, 1125 Budapest, Hungary.
Nadim Al-MuhannaDepartment of Neurology and Stroke, Saint John's Central Hospital of North Buda, 1125 Budapest, Hungary.
Richard SchwabMiND Brain-Gut Center, 1125 Budapest, Hungary.ORCID 0009-0000-7014-1667
Viktoria HadnagyMiND Brain-Gut Center, 1125 Budapest, Hungary.
Sara LakiMiND Brain-Gut Center, 1125 Budapest, Hungary.
Janos Tamas VargaDepartment of Pulmonology, Semmelweis University, 1083 Budapest, Hungary.ORCID 0000-0002-8552-1336
Andrea LehoczkiHealth Sciences Division, Doctoral College, Semmelweis University, 1085 Budapest, Hungary.
Virag ZaboHealth Sciences Division, Doctoral College, Semmelweis University, 1085 Budapest, Hungary.
Diana GorogFaculty of International Business Economics, Budapest University of Economics and Business, 1054 Budapest, Hungary.
Monika FeketeHealth Sciences Division, Doctoral College, Semmelweis University, 1085 Budapest, Hungary.ORCID 0000-0001-8632-2120

Funding

National Cardiovascular Laboratory Program RRF-2.3.1-21-2022-00003National Research, Development and Innovation Office TKP2021-NKTA-47
6 · The paper itself

Abstract

BACKGROUND/

objectivesCerebral small vessel disease (CSVD) is a major vascular component of brain aging, yet potentially modifiable systemic contributors remain incompletely understood. Growing evidence links the gut microbiome to magnetic resonance imaging (MRI)-defined CSVD, but interpretation is complicated by heterogeneity in microbiome profiling, clinical populations, analytical methods, and neuroimaging phenotypes. This review critically integrates the available human evidence with complementary multi-omics, ex vivo, and experimental findings.

methodsPubMed, Embase, Scopus, and Web of Science were searched through 4 August 2026; 12 eligible reports representing eight cohort families were included and evaluated using a structured study-level methodological appraisal.

resultsAcross the available literature, ecological and host-related biological processes show greater qualitative convergence than individual taxa, although this pattern has not been formally quantified across independent cohorts. Among reported alpha diversity measures, Chao/Chao1 showed the same numerical disease-versus-control direction across four cohort families, with statistical significance in two, suggesting a recurrent but still preliminary richness-related signal; Shannon and Simpson indices were less consistent. No single genus or species has been consistently replicated across the available, largely cross-sectional cohorts. Complementary studies implicate intestinal barrier, immune-metabolic, neurovascular, and perivascular clearance pathways but do not establish a unified causal pathway in human sporadic CSVD.

conclusionsThese observations support a hypothesis-generating ecosystem-level framework. Because diet is an important modifiable determinant of the gut microbial ecosystem, these findings may have relevance for nutrition-based strategies targeting vascular brain aging. However, no CSVD-specific dietary or microbiome-directed intervention has yet been shown to modify disease progression or related MRI outcomes.

Indexed as

AgingBrainCerebral Small Vessel DiseasesGastrointestinal MicrobiomeAgedFemaleHumansMagnetic Resonance ImagingMalePhenotypebrain agingcerebral small vessel diseasegut–brain axisgut microbiomemagnetic resonance imagingmicrobial richnessvascular cognitive impairmentwhite matter hyperintensities

Identifiers

PMID42942992
PMCPMC13708570

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.