Evidence map›Paper›PMID 40236713›Full record

ArticleFrontiers in immunology2025

Vegetal oil-based ketogenic diet improves inflammation and fibrosis in experimental metabolic dysfunction-associated steatohepatitis.

Alessia Provera, Naresh Naik Ramavath, Laila Lavanya Gadipudi, Cristina Vecchio, Marina Caputo, Alessandro Antonioli, Sabrina Tini, Anteneh Nigussie Sheferaw, Simone Reano, Nicoletta Filigheddu and 10 more

Abstract read
In one paragraph

Article in Frontiers in immunology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

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  6. 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

20 authors.

Alessia ProveraDepartment of Health Sciences and Interdisciplinary Research Centre for Autoimmune Diseases, University of Piemonte Orientale, Novara, Italy.
Naresh Naik RamavathDepartment of Health Sciences and Interdisciplinary Research Centre for Autoimmune Diseases, University of Piemonte Orientale, Novara, Italy.
Laila Lavanya GadipudiDepartment of Health Sciences and Interdisciplinary Research Centre for Autoimmune Diseases, University of Piemonte Orientale, Novara, Italy.
Cristina VecchioDepartment of Health Sciences and Interdisciplinary Research Centre for Autoimmune Diseases, University of Piemonte Orientale, Novara, Italy.
Marina CaputoDepartment of Health Sciences and Interdisciplinary Research Centre for Autoimmune Diseases, University of Piemonte Orientale, Novara, Italy.
Alessandro AntonioliDepartment of Health Sciences and Interdisciplinary Research Centre for Autoimmune Diseases, University of Piemonte Orientale, Novara, Italy.
Sabrina TiniDepartment of Health Sciences and Interdisciplinary Research Centre for Autoimmune Diseases, University of Piemonte Orientale, Novara, Italy.
Anteneh Nigussie SheferawDepartment of Health Sciences and Interdisciplinary Research Centre for Autoimmune Diseases, University of Piemonte Orientale, Novara, Italy.
Simone ReanoDepartment of Translational Medicine, University of Piemonte Orientale, Novara, Italy.
Nicoletta FilighedduDepartment of Translational Medicine, University of Piemonte Orientale, Novara, Italy.
Marcello ManfrediDepartment of Translational Medicine, University of Piemonte Orientale, Novara, Italy.
Elettra BarberisDepartment of Sciences and Technological Innovation, University of Piemonte Orientale, Alessandria, Italy.
Luca CocolinDepartment of Agricultural, Forestry and Food Science, University of Torino, Grugliasco, Italy.
Ilario FerrocinoDepartment of Agricultural, Forestry and Food Science, University of Torino, Grugliasco, Italy.
Monica LocatelliDepartment of Pharmaceutical Sciences, University of Piemonte Orientale, Novara, Italy.
Massimiliano CaprioDepartment of Human Sciences and Promotion of the Quality of Life, San Raffaele Roma Open University, Rome, Italy.
Frank TackeDepartment of Hepatology & Gastroenterology, Charité - Universitätsmedizin Berlin, Berlin, Germany.
Emanuele AlbanoDepartment of Health Sciences and Interdisciplinary Research Centre for Autoimmune Diseases, University of Piemonte Orientale, Novara, Italy.
Flavia ProdamDepartment of Health Sciences and Interdisciplinary Research Centre for Autoimmune Diseases, University of Piemonte Orientale, Novara, Italy.
Salvatore SuttiDepartment of Health Sciences and Interdisciplinary Research Centre for Autoimmune Diseases, University of Piemonte Orientale, Novara, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background and aims: Metabolic dysfunction-associated steatohepatitis (MASH) represents a growing cause of liver cirrhosis and hepatocellular carcinoma (HCC). However, effective therapy for MASH is still lacking. Despite recent studies suggest that ketosis might improve MASH evolution, the mechanisms involved have not been explored since common ketogenic diets cause severe steatohepatitis in mice. In this study, we have investigated the capacity of a new-formulated ketogenic diet (KD) containing vegetal fat in improving liver alterations associated with experimental MASH. Methods: MASH was induced in C57BL/6 mice by feeding a cholesterol-enriched Western Diet (WD) for up to 16 weeks, followed by switching animals to KD for an additional eight weeks. Results: We observed that KD administration greatly increased ketone body production and significantly reduced liver and body weights. Moreover, liver proteomic analysis and functional tests evidenced an improved glucose and lipid metabolism along with insulin resistance in KD-fed mice. These metabolic effects were associated with an amelioration in MASH-associated gut dysbiosis and with an improvement of hepatic steatosis, parenchymal injury and liver fibrosis. From the mechanistic point of view mice receiving KD showed a significant reduction in liver TREM2-positive monocyte-derived macrophages forming crown-like aggregates along with a lowering in the hepatic expression of pro-inflammatory/pro-fibrogenic markers such as CCL2, IL-12, CD11b, α1-procollagen, TGF-β1, osteopontin, and galectin-3. Consistently, Conclusions: Altogether, these results indicate that ketogenic diet based on vegetal fat effectively improves MASH metabolic derangements and steatohepatitis, and it might represent a potential therapeutic strategy in this disease.

Indexed as

Diet, KetogenicFatty LiverLiver CirrhosisNon-alcoholic Fatty Liver DiseaseAnimalsDisease Models, AnimalInflammationLipid MetabolismLiverMaleMiceMice, Inbred C57BLgut dysbiosisketone bodiesliver fibrosisliver inflammationmetabolic dysfunction-associated steatotic liver diseasenon-alcoholic fatty liver diseasenon-alcoholic steatohepatitis

Identifiers

PMID40236713
PMCPMC11996634

What Socratic holds

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LicenceCC BY
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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 Socratic graph.