Evidence map›Paper›PMID 40796226›Full record

ReviewAmerican journal of physiology. Gastrointestinal and liver physiology2025

The synergistic interplay between vitamin A, dietary fiber, and the microbiota-gut-brain axis: a potential mechanism for preventing Alzheimer's disease.

Shadt Skawratananond, Grace E McCrea, Paul Lie, Matthew B Buxton, Sean P Daly, Nicholas A Vojtkofsky, Shane C Smith, Charlie Zhang, Matthew Hernandez, Ashly Hindle and 2 more

Abstract readReview
In one paragraph

Review in American journal of physiology. Gastrointestinal and liver physiology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

8 citing papers in PubMed.

  1. Article
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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

12 authors.

Shadt SkawratananondDepartment of Pharmacology and Neuroscience, Texas Tech University Health Sciences Center, Lubbock, Texas, United States.ORCID 0009-0008-0737-4626
Grace E McCreaDepartment of Pharmacology and Neuroscience, Texas Tech University Health Sciences Center, Lubbock, Texas, United States.
Paul LieDepartment of Pharmacology and Neuroscience, Texas Tech University Health Sciences Center, Lubbock, Texas, United States.ORCID 0000-0003-0166-2674
Matthew B BuxtonDepartment of Pharmacology and Neuroscience, Texas Tech University Health Sciences Center, Lubbock, Texas, United States.
Sean P DalySchool of Medicine, Texas Tech University Health Sciences Center, Lubbock, Texas, United States.
Nicholas A VojtkofskyDepartment of Pharmacology and Neuroscience, Texas Tech University Health Sciences Center, Lubbock, Texas, United States.
Shane C SmithDepartment of Pharmacology and Neuroscience, Texas Tech University Health Sciences Center, Lubbock, Texas, United States.ORCID 0009-0003-6273-4149
Charlie ZhangDepartment of Pharmacology and Neuroscience, Texas Tech University Health Sciences Center, Lubbock, Texas, United States.ORCID 0009-0002-3550-6098
Matthew HernandezDepartment of Pharmacology and Neuroscience, Texas Tech University Health Sciences Center, Lubbock, Texas, United States.
Ashly HindleDepartment of Pharmacology and Neuroscience, Texas Tech University Health Sciences Center, Lubbock, Texas, United States.
Aric F LogsdonDepartment of Pharmacology and Neuroscience, Texas Tech University Health Sciences Center, Lubbock, Texas, United States.ORCID 0000-0001-6379-4838
J Josh LawrenceDepartment of Pharmacology and Neuroscience, Texas Tech University Health Sciences Center, Lubbock, Texas, United States.ORCID 0000-0002-9068-0841

Funding

The hippocampal dentate gyrus in aging and Alzheimer's disease: boosting transcription of retinoic acid-sensitive genes through vitamin A supplementation and HDAC inhibitionR01AG073826 · NIA · TEXAS TECH UNIVERSITY HEALTH SCIS CENTER · PI John Joshua Lawrence · 2022 to 2026
$3.1M
Transcriptional Dysfunction in Dentate Gyrus Cell Types: Roles of Retinoic Acid Responsive Genes in Protection Against Alzheimer's Disease PathogenesisR01AG071859 · NIA · TEXAS TECH UNIVERSITY HEALTH SCIS CENTER · PI John Joshua Lawrence · 2022 to 2026
$1.9M
Targeting mechanisms of glycosaminoglycan accumulation and neurobehavioral dysfunction to improve outcomes from traumatic brain injuryK22AG081264 · NIA · TEXAS TECH UNIVERSITY HEALTH SCIS CENTER · PI Aric Flint Logsdon · 2025 to 2026
$385k
HHS | NIH | National Institute on Aging (NIA) AG071859HHS | NIH | National Institute on Aging (NIA) AG073826NIA NIH HHS K22 AG081264NIA NIH HHS R01 AG071859NIA NIH HHS R01 AG073826Texas Tech University Health Sciences Center (TTUHSC) MSSRP
6 · The paper itself

Abstract

The human gastrointestinal tract harbors a vast and diverse microbial community, with the gut microbiome playing a fundamental role in numerous biological processes that influence overall health and disease progression. Emerging evidence has identified bacterial lipopolysaccharides in the hippocampus of patients with Alzheimer's disease (AD), highlighting the intricate relationship between the gastrointestinal tract, gut microbiome, and the central and enteric nervous systems-commonly referred to as the "microbiota-gut-brain axis." In this review, we explore the mechanisms by which the microbiota-gut-brain axis contributes to AD pathogenesis. We propose that sufficient levels of all-trans retinoic acid (ATRA), the bioactive form of vitamin A, enhance intestinal barrier integrity by upregulating tight junction proteins and modulating immune function through the induction of regulatory T-cell differentiation, thereby mitigating inflammation. Furthermore, dietary fiber complements this process by promoting the production of short-chain fatty acids, such as butyrate, via bacterial fermentation. Butyrate, in turn, acts as a histone deacetylase inhibitor, upregulating ATRA bioavailability by elevating aldehyde dehydrogenase gene expression. Our mechanistic framework is supported by the endotoxin hypothesis of AD, which maintains that the movement of infectious pathogens across the blood-brain barrier causes a vicious cycle of inflammation, a key factor of AD pathogenesis, leading to amyloid-β deposition, microglial activation, and CYP26A1-mediated ATRA degradation. Finally, we discuss microbiome-based therapeutic strategies and dietary interventions, including prebiotic compounds, probiotic bacteria, fecal microbiota transplantation, the Mediterranean-DASH Intervention for Neurodegenerative Delay (MIND) diet, and a combined approach featuring vitamins A/D and dietary fiber, as potential approaches to prevent progression to AD via the microbiota-gut-brain axis.

Indexed as

Alzheimer DiseaseBrainBrain-Gut AxisDietary FiberGastrointestinal MicrobiomeVitamin AAnimalsHumansDietary FiberVitamin Aall-trans retinoic acidAlzheimer’s diseasebutyratelipopolysaccharidemicrobiota-gut-brain axis

Identifiers

PMID40796226
PMCPMC12622890

What OpenQuestion holds

Textmetadata
LicenceTDM
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.