Evidence map›Paper›PMID 30586623›Full record

ArticleCellular and molecular gastroenterology and hepatology2019

A High-Calorie Diet Aggravates Mitochondrial Dysfunction and Triggers Severe Liver Damage in Wilson Disease Rats.

Claudia Einer, Christin Leitzinger, Josef Lichtmannegger, Carola Eberhagen, Tamara Rieder, Sabine Borchard, Ralf Wimmer, Gerald Denk, Bastian Popper, Frauke Neff and 13 more

Open access · goldAbstract read
In one paragraph

Article in Cellular and molecular gastroenterology and hepatology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed, 1 pooled it
4.7field-weighted citation impact, top 4% 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

41 citing papers in PubMed, 1 synthesis or guideline pooled it, 69 citations in OpenAlex.

  1. Pooled it
  2. Cuproptosis in iron overload hepatocytes.Cell death & disease · 2026
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  4. Review
  5. Review
  6. Article
  7. Review
  8. Article
  9. Article
  10. Review
  11. Review
  12. Article
  13. Article
  14. Crystal structure of MbnF: an NADPH-dependent flavin monooxygenase from Methylocystis strain SB2.Acta crystallographica. Section F, Structural biology communications · 2023
    Article
  15. Article
  16. Is Prolonged Copper Restriction Needed in Pediatric Wilson's Disease?The Turkish journal of gastroenterology : the official journal of Turkish Society of Gastroenterology · 2023
    Article
  17. Article
  18. Review
  19. Article
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

23 authors at 9 institutions in 3 countries.

Claudia EinerInstitute of Molecular Toxicology and Pharmacology, Helmholtz Center Munich, German Research Center for Environmental Health, Neuherberg, Germany; Department of Medicine II, University Hospital, Ludwig-Maximilians-University Munich, Munich, Germany.
Christin LeitzingerInstitute of Molecular Toxicology and Pharmacology, Helmholtz Center Munich, German Research Center for Environmental Health, Neuherberg, Germany.
Josef LichtmanneggerInstitute of Molecular Toxicology and Pharmacology, Helmholtz Center Munich, German Research Center for Environmental Health, Neuherberg, Germany.
Carola EberhagenInstitute of Molecular Toxicology and Pharmacology, Helmholtz Center Munich, German Research Center for Environmental Health, Neuherberg, Germany.
Tamara RiederInstitute of Toxicology and Environmental Hygiene, Technical University Munich, Munich, Germany.
Sabine BorchardInstitute of Molecular Toxicology and Pharmacology, Helmholtz Center Munich, German Research Center for Environmental Health, Neuherberg, Germany.
Ralf WimmerDepartment of Medicine II, University Hospital, Ludwig-Maximilians-University Munich, Munich, Germany.
Gerald DenkDepartment of Medicine II, University Hospital, Ludwig-Maximilians-University Munich, Munich, Germany.
Bastian PopperDepartment of Anatomy and Cell Biology, Biomedical Center, Ludwig-Maximilians-University, Planegg-Martinsried, Germany; Core Facility Animal Models, Biomedical Center, Ludwig-Maximilians-University, Planegg-Martinsried, Germany.
Frauke NeffInstitute of Pathology, Helmholtz Center Munich, German Research Center for Environmental Health, Neuherberg, Germany.
Elena V PolishchukTelethon Institute of Genetics and Medicine, Pozzuoli (Naples), Italy.
Roman S PolishchukTelethon Institute of Genetics and Medicine, Pozzuoli (Naples), Italy.
Stefanie M HauckResearch Unit Protein Science, Helmholtz Center Munich, German Research Center for Environmental Health, Neuherberg, Germany.
Christine von ToerneResearch Unit Protein Science, Helmholtz Center Munich, German Research Center for Environmental Health, Neuherberg, Germany.
Jennifer-Christin MüllerInstitute of Inorganic and Analytical Chemistry, University of Münster, Münster, Germany.
Uwe KarstInstitute of Inorganic and Analytical Chemistry, University of Münster, Münster, Germany.
Bipin S BaralRoy J. Carver Department of Biochemistry, Biophysics and Molecular Biology, Iowa State University, Ames, Iowa.
Alan A DiSpiritoRoy J. Carver Department of Biochemistry, Biophysics and Molecular Biology, Iowa State University, Ames, Iowa.
Andreas E KremerDepartment of Medicine I, Friedrich-Alexander-University Erlangen-Nürnberg, Erlangen, Germany.
Jeremy SemrauDepartment of Civil and Environmental Engineering, University of Michigan, Ann Arbor, Michigan.
Karl Heinz WeissDepartment of Gastroenterology, Internal Medicine IV, University Hospital Heidelberg, Heidelberg, Germany.
Simon HohenesterDepartment of Medicine II, University Hospital, Ludwig-Maximilians-University Munich, Munich, Germany.
Hans ZischkaInstitute of Molecular Toxicology and Pharmacology, Helmholtz Center Munich, German Research Center for Environmental Health, Neuherberg, Germany; Institute of Toxicology and Environmental Hygiene, Technical University Munich, Munich, Germany. Electronic address: zischka@helmholtz-muenchen.de.
Helmholtz Zentrum München · DELudwig-Maximilians-Universität München · DEIowa State University · USTelethon Institute Of Genetics And Medicine · ITUniversity of Münster · DEFriedrich-Alexander-Universität Erlangen-Nürnberg · DEHeidelberg University · DETechnical University of Munich · DEUniversity of Michigan · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND &

aimsIn Wilson disease, ATP7B mutations impair copper excretion into bile. Hepatic copper accumulation may induce mild to moderate chronic liver damage or even acute liver failure. Etiologic factors for this heterogeneous phenotype remain enigmatic. Liver steatosis is a frequent finding in Wilson disease patients, suggesting that impaired copper homeostasis is linked with liver steatosis. Hepatic mitochondrial function is affected negatively both by copper overload and steatosis. Therefore, we addressed the question of whether a steatosis-promoting high-calorie diet aggravates liver damage in Wilson disease via amplified mitochondrial damage.

methodsControl Atp7b

resultsIn comparison with a normal diet, HCD feeding of Atp7b

conclusionsA high-calorie diet severely aggravates hepatic mitochondrial and hepatocellular damage in Wilson disease rats, causing an earlier onset of the disease and enhanced disease progression.

Indexed as

DietAnimalsBile Acids and SaltsCopperCopper-Transporting ATPasesDisease ProgressionFatty LiverFemaleHepatocytesHepatolenticular DegenerationInflammationLipidsLiverMaleMitochondriaPeptidesAtp7b protein, ratBile Acids and SaltsCopperCopper-Transporting ATPasesLipidsPeptidesProteomeCopper-Storage DiseaseMethanobactinMitochondriaSteatohepatitisSteatosis

Identifiers

PMID30586623
PMCPMC6407159
OpenAlexW2906008434

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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 OpenQuestion graph.