Evidence map›Paper›PMID 24327959›Full record

ArticleMolecular metabolism2013

Phenotypic comparison of common mouse strains developing high-fat diet-induced hepatosteatosis.

Melanie Kahle, Marion Horsch, Barbara Fridrich, Anett Seelig, Jürgen Schultheiß, Jörn Leonhardt, Martin Irmler, Johannes Beckers, Birgit Rathkolb, Eckhard Wolf and 5 more

Open access · goldAbstract read
In one paragraph

Article in Molecular metabolism, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 46 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
46citing papers in PubMed, 1 pooled it
4.3field-weighted citation impact, top 5% 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

46 citing papers in PubMed, 1 synthesis or guideline pooled it, 59 citations in OpenAlex.

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  17. Vanin 1: Its Physiological Function and Role in Diseases.International journal of molecular sciences · 2019
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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

15 authors at 3 institutions in 1 country.

Melanie KahleInstitute of Experimental Genetics, Helmholtz Zentrum München, German Research Center for Environmental Health, Ingolstädter Landstrasse 1, 85764 Neuherberg/Munich, Germany ; German Center for Diabetes Research (DZD), Ingolstädter Landstraße 1, 85764 Neuherberg/Munich, Germany.
Marion Horsch
Barbara Fridrich
Anett Seelig
Jürgen Schultheiß
Jörn Leonhardt
Martin Irmler
Johannes Beckers
Birgit Rathkolb
Eckhard Wolf
Nicole Franke
Valérie Gailus-Durner
Helmut Fuchs
Martin Hrabě de Angelis
Susanne Neschen
Helmholtz Zentrum München · DELudwig-Maximilians-Universität München · DEInstitute of Bioinformatics and Systems Biology · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Genetic predisposition and environmental factors contribute to an individual's susceptibility to develop hepatosteatosis. In a systematic, comparative survey we focused on genotype-dependent and -independent adaptations early in the pathogenesis of hepatosteatosis by characterizing C3HeB/FeJ, C57BL/6NTac, C57BL/6J, and 129P2/OlaHsd mice after 7, 14, or 21 days high-fat-diet exposure. Strain-specific metabolic responses during diet challenge and liver transcript signatures in mild hepatosteatosis outline the suitability of particular strains for investigating the relationship between hepatocellular lipid content and inflammation, glucose homeostasis, insulin action, or organelle physiology. Genetic background-independent transcriptional adaptations in liver paralleling hepatosteatosis suggest an early increase in the organ's vulnerability to oxidative stress damage what could advance hepatosteatosis to steatohepatitis. "Universal" adaptations in transcript signatures and transcription factor regulation in liver link insulin resistance, type 2 diabetes mellitus, cancer, and thyroid hormone metabolism with hepatosteatosis, hence, facilitating the search for novel molecular mechanisms potentially implicated in the pathogenesis of human non-alcoholic-fatty-liver-disease.

Indexed as

129, 129P2/OlaHsdALT, alanine aminotransferaseB6J, C57BL/6JB6N, C57BL/6NTacC3H, C3HeB/FeJCancerHDL, high-density lipoproteinHFD, high-fat dietInflammationInsulin resistanceIR, insulin resistanceLDL, low-density lipoproteinLFD, low fat rodent laboratory dietNAFLD, non-alcoholic fatty liver diseaseNASH, non-alcoholic hepatosteatitisNon-alcoholic fatty liver diseaseOxidative stressT2D, type 2 diabetes mellitusTAG, triacylglycerolThyroid metabolismVLDL, very low density lipoproteinWAT, white adipose tissue

Identifiers

PMID24327959
PMCPMC3855089
OpenAlexW2020507606

What OpenQuestion holds

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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.