Evidence map›Paper›PMID 42905751›Full record

SynthesisPloS one2026

Dietary context and ethanol-related injury in preclinical models: A contemporary systematic review of predominantly obesogenic diets and liver outcomes.

Worship O Agbonifo, Joseph Chimezie, Zainab A Amoo, Chidinma Chukwukaeme, Hope O Francis, Mercy O Awoleye, Temitope G Adedeji

Abstract readSystematic Review
In one paragraph

Synthesis in PloS one, 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

7 authors.

Worship O AgbonifoEpigenetics and Molecular Biology Laboratory, Federal University of Technology, Akure, Nigeria.ORCID https://orcid.org/0000-0002-7023-2056
Joseph ChimezieEpigenetics and Molecular Biology Laboratory, Federal University of Technology, Akure, Nigeria.
Zainab A AmooEpigenetics and Molecular Biology Laboratory, Federal University of Technology, Akure, Nigeria.
Chidinma ChukwukaemeDepartment of Physiology, Michigan State University, East Lansing, Michigan, United States of America.
Hope O FrancisEpigenetics and Molecular Biology Laboratory, Federal University of Technology, Akure, Nigeria.
Mercy O AwoleyeEpigenetics and Molecular Biology Laboratory, Federal University of Technology, Akure, Nigeria.
Temitope G AdedejiEpigenetics and Molecular Biology Laboratory, Federal University of Technology, Akure, Nigeria.ORCID https://orcid.org/0000-0001-6697-2708

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Diet composition is an important food-derived exposure that may influence alcohol-related tissue injury. However, evidence on how specific dietary contexts modify ethanol-induced injury and its underlying biological mechanisms in controlled preclinical models remains fragmented. This systematic review examined whether defined dietary patterns modify ethanol-related injury in controlled mammalian studies. Following PRISMA 2020, PubMed, Embase, and Scopus were searched for studies published from January 2021 to January 15, 2026. Eligible studies were controlled in vivo mammalian experiments comparing ethanol exposure under defined dietary patterns. Evidence was narratively synthesized by diet type, organ system, and mechanism; random-effects meta-analyses and prespecified interaction analyses were conducted when sufficiently comparable data were available. Twenty-seven studies met the inclusion criteria (24 mouse and three rat studies); 18 used male-only animals, most examined high-fat or Western-type diets, and liver outcomes predominated. Evidence for non-obesogenic diets was limited to one ketogenic-diet study. In acute high-fat-diet models, adding ethanol increased serum ALT (SMD 2.31, 95% CI 1.46-3.16), AST (SMD 1.18, 95% CI 0.54-1.81), and hepatic triglycerides (SMD 2.06, 95% CI 0.96-3.17). Acute interaction analysis identified dietary effect modification only for ALT (MD 74.56, 95% CI 59.03-90.10), while chronic analyses showed a negative interaction for hepatic triglycerides (MD -0.048, 95% CI -0.092 to -0.004; P = 0.03). Extrahepatic, microbiome, and multi-omics findings were sparse and heterogeneous. High-fat and Western-type diets generally exacerbated ethanol-induced hepatic injury, whereas evidence for other dietary patterns remains limited.

Indexed as

DietEthanolLiverObesityAnimalsDiet, High-FatDisease Models, AnimalHumansMaleMiceRatsEthanol

Identifiers

PMID42905751
PMCPMC13686270

What OpenQuestion holds

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Registered trials

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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.