Evidence mapPaperPMID 37683301Full record

ArticleRedox biology2023

TNFα is a key trigger of inflammation in diet-induced non-obese MASLD in mice.

Katharina Burger, Finn Jung, Anja Baumann, Annette Brandt, Raphaela Staltner, Victor Sánchez, Ina Bergheim

Open access · goldAbstract read
In one paragraph

Article in Redox biology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
6.0field-weighted citation impact, top 3% of its field
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

22 citing papers in PubMed, 28 citations in OpenAlex.

  1. Article
  2. Review
  3. Burden of MASLD and liver fibrosis: evidence from Phenome India cohort.The Lancet regional health. Southeast Asia · 2026
    Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Mediation analysis of the molecular phenotypes in a severe MASH-like liver injury mouse model.Toxicological sciences : an official journal of the Society of Toxicology · 2025
    Article
  10. Article
  11. Review
  12. Review
  13. Article
  14. Article
  15. Targeting Metabolism: Innovative Therapies for MASLD Unveiled.International journal of molecular sciences · 2025
    Review
  16. Article
  17. Review
  18. Article
  19. Review
  20. Antioxidant and Anti-Inflammatory Effects ofAntioxidants (Basel, Switzerland) · 2024
    Article
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 at 1 institution in 1 country.

Katharina BurgerDepartment of Nutritional Sciences, Molecular Nutritional Science, University of Vienna, Vienna, Austria.
Finn JungDepartment of Nutritional Sciences, Molecular Nutritional Science, University of Vienna, Vienna, Austria.
Anja BaumannDepartment of Nutritional Sciences, Molecular Nutritional Science, University of Vienna, Vienna, Austria.
Annette BrandtDepartment of Nutritional Sciences, Molecular Nutritional Science, University of Vienna, Vienna, Austria.
Raphaela StaltnerDepartment of Nutritional Sciences, Molecular Nutritional Science, University of Vienna, Vienna, Austria.
Victor SánchezDepartment of Nutritional Sciences, Molecular Nutritional Science, University of Vienna, Vienna, Austria.
Ina BergheimDepartment of Nutritional Sciences, Molecular Nutritional Science, University of Vienna, Vienna, Austria. Electronic address: ina.bergheim@univie.ac.at.
University of Vienna · AT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Tumor necrosis factor alpha (TNFα) is thought to be a critical factor in the development of metabolic dysfunction-associated steatotic liver disease (MASLD). Here, we determined the effects of a treatment with the anti-TNFα antibody infliximab and a genetic deletion of TNFα, respectively, in the development of non-obese diet-induced early metabolic dysfunction-associated steatohepatitis (MASH) in mice. The treatment with infliximab improved markers of liver damage in mice with pre-existing early MASH. In TNFα

Indexed as

Fatty LiverInsulin ResistanceMetabolic DiseasesAnimalsDietInflammationInfliximabMiceTumor Necrosis Factor-alphaInfliximabTumor Necrosis Factor-alphaEndotoxinFatty liverInsulin resistanceIntestinal barrierMASH

Identifiers

PMID37683301
PMCPMC10493600
OpenAlexW4386385191

What Socratic holds

Textmetadata
LicenceCC BY
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 Socratic graph.