Evidence map›Paper›PMID 27981604›Full record

ArticleHepatology (Baltimore, Md.)2017

Malondialdehyde epitopes are sterile mediators of hepatic inflammation in hypercholesterolemic mice.

Clara Jana-Lui Busch, Tim Hendrikx, David Weismann, Sven Jäckel, Sofie M A Walenbergh, André F Rendeiro, Juliane Weißer, Florian Puhm, Anastasiya Hladik, Laura Göderle and 10 more

Open access · bronzeAbstract readComparative Study
In one paragraph

Article in Hepatology (Baltimore, Md.), 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 45 papers.

0numbers the graph read from it
0cells of the map it votes in
45citing papers in PubMed
3.6field-weighted citation impact, top 7% 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

45 citing papers in PubMed, 66 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. IgM Antibodies Targeting Malondialdehyde Promote Complement-Mediated Liver Injury in Alcohol-Related Liver Disease.Liver international : official journal of the International Association for the Study of the Liver · 2025
    Article
  5. Review
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  7. Therapeutic Strategies for MASH: An Update on Drug Candidates Under Investigation in Late-Phase Clinical Trials.International journal of translational medicine (Basel, Switzerland) · 2025
    Article
  8. Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Review
  15. Article
  16. Article
  17. Article
  18. MCD Diet Modulates HuR and Oxidative Stress-Related HuR Targets in Rats.International journal of molecular sciences · 2023
    Article
  19. Article
  20. 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

20 authors at 6 institutions in 3 countries.

Clara Jana-Lui BuschDepartment of Laboratory Medicine, Medical University of Vienna, Vienna, Austria.
Tim HendrikxDepartment of Laboratory Medicine, Medical University of Vienna, Vienna, Austria.
David WeismannDepartment of Laboratory Medicine, Medical University of Vienna, Vienna, Austria.
Sven JäckelCenter for Thrombosis and Haemostasis, University Medical Center Mainz, Mainz, Germany.
Sofie M A WalenberghDepartment of Molecular Genetics, School of Nutrition and Translational Research in Metabolism, Maastricht University, Maastricht, The Netherlands.
André F RendeiroCeMM Research Center for Molecular Medicine of the Austrian Academy of Sciences, Vienna, Austria.
Juliane WeißerCeMM Research Center for Molecular Medicine of the Austrian Academy of Sciences, Vienna, Austria.
Florian PuhmDepartment of Laboratory Medicine, Medical University of Vienna, Vienna, Austria.
Anastasiya HladikCeMM Research Center for Molecular Medicine of the Austrian Academy of Sciences, Vienna, Austria.
Laura GöderleDepartment of Laboratory Medicine, Medical University of Vienna, Vienna, Austria.
Nikolina Papac-MilicevicDepartment of Laboratory Medicine, Medical University of Vienna, Vienna, Austria.
Gerald HaasDepartment of Laboratory Medicine, Medical University of Vienna, Vienna, Austria.
Vincent MillischerDepartment of Laboratory Medicine, Medical University of Vienna, Vienna, Austria.
Saravanan SubramaniamCenter for Thrombosis and Haemostasis, University Medical Center Mainz, Mainz, Germany.
Sylvia KnappCeMM Research Center for Molecular Medicine of the Austrian Academy of Sciences, Vienna, Austria.
Keiryn L BennettCeMM Research Center for Molecular Medicine of the Austrian Academy of Sciences, Vienna, Austria.
Christoph BockDepartment of Laboratory Medicine, Medical University of Vienna, Vienna, Austria.
Christoph ReinhardtCenter for Thrombosis and Haemostasis, University Medical Center Mainz, Mainz, Germany.
Ronit Shiri-SverdlovDepartment of Molecular Genetics, School of Nutrition and Translational Research in Metabolism, Maastricht University, Maastricht, The Netherlands.
Christoph J BinderDepartment of Laboratory Medicine, Medical University of Vienna, Vienna, Austria.
Austrian Academy of Sciences · ATMedical University of Vienna · ATCeMM Research Center for Molecular Medicine · ATMaastricht University · NLUniversity Medical Center of the Johannes Gutenberg University Mainz · DEGerman Centre for Cardiovascular Research · DE

Funding

Austrian Science Fund FWF F 3015
6 · The paper itself

Abstract

Diet-related health issues such as nonalcoholic fatty liver disease and cardiovascular disorders are known to have a major inflammatory component. However, the exact pathways linking diet-induced changes (e.g., hyperlipidemia) and the ensuing inflammation have remained elusive so far. We identified biological processes related to innate immunity and oxidative stress as prime response pathways in livers of low-density lipoprotein receptor-deficient mice on a Western-type diet using RNA sequencing and in silico functional analyses of transcriptome data. The observed changes were independent of the presence of microbiota and thus indicative of a role for sterile triggers. We further show that malondialdehyde (MDA) epitopes, products of lipid peroxidation and markers for enhanced oxidative stress, are detectable in hepatic inflammation predominantly on dying cells and stimulate cytokine secretion as well as leukocyte recruitment in vitro and in vivo. MDA-induced cytokine secretion in vitro was dependent on the presence of the scavenger receptors CD36 and MSR1. Moreover, in vivo neutralization of endogenously generated MDA epitopes by intravenous injection of a specific MDA antibody results in decreased hepatic inflammation in low-density lipoprotein receptor-deficient mice on a Western-type diet.

conclusionAccumulation of MDA epitopes plays a major role during diet-induced hepatic inflammation and can be ameliorated by administration of an anti-MDA antibody. (Hepatology 2017;65:1181-1195).

Indexed as

Diet, WesternAnalysis of VarianceAnimalsBiopsy, NeedleCytokinesDisease Models, AnimalEpitopesFatty LiverFemaleHypercholesterolemiaImmunity, InnateImmunohistochemistryInflammation MediatorsLipid PeroxidationMalondialdehydeMiceCytokinesEpitopesInflammation MediatorsMalondialdehyde

Identifiers

PMID27981604
PMCPMC5892702
OpenAlexW2565209260

What OpenQuestion holds

Textmetadata
LicenceTDM
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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.