Evidence map›Paper›PMID 30556039›Full record

ArticleHepatology communications2018

Obeticholic Acid Modulates Serum Metabolites and Gene Signatures Characteristic of Human NASH and Attenuates Inflammation and Fibrosis Progression in Ldlr-/-.Leiden Mice.

Martine C Morrison, Lars Verschuren, Kanita Salic, Joanne Verheij, Aswin Menke, Peter Y Wielinga, Marta Iruarrizaga-Lejarreta, Laurent Gole, Wei-Miao Yu, Scott Turner and 10 more

Open access · goldAbstract read
In one paragraph

Article in Hepatology communications, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed
3.7field-weighted citation impact, top 6% 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

40 citing papers in PubMed, 56 citations in OpenAlex.

  1. Article
  2. Review
  3. Fibrogenic Gene Signature as Early Prediction for the Efficacy of Pharmacological Interventions for MASH-Associated Fibrosis.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2025
    Article
  4. Therapeutic effects of FGF21 mimetic bFKB1 on MASH and atherosclerosis in Ldlr-/-.Leiden mice.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2024
    Article
  5. Review
  6. Article
  7. Schisandrin A inJournal of microbiology and biotechnology · 2024
    Article
  8. Review
  9. Dysfunctional VLDL metabolism in MASLD.npj metabolic health and disease · 2024
    Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Review
  15. Review
  16. ALS-L1023 fromLife (Basel, Switzerland) · 2022
    Article
  17. Article
  18. Review
  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 5 institutions in 4 countries.

Martine C MorrisonDepartment of Metabolic Health Research Netherlands Organization for Applied Scientific Research Leiden The Netherlands.ORCID 0000-0003-4996-943X
Lars VerschurenDepartment of Microbiology and Systems Biology Netherlands Organisation for Applied Scientific Research Zeist The Netherlands.
Kanita SalicDepartment of Metabolic Health Research Netherlands Organization for Applied Scientific Research Leiden The Netherlands.
Joanne VerheijDepartment of Pathology Amsterdam Medical Center Amsterdam The Netherlands.
Aswin MenkeDepartment of Pathology Triskelion B.V. Zeist The Netherlands.
Peter Y WielingaDepartment of Metabolic Health Research Netherlands Organization for Applied Scientific Research Leiden The Netherlands.
Marta Iruarrizaga-LejarretaOWL Metabolomics Derio Spain.
Laurent GoleComputational BioImage Analysis Unit, Agency of Science, Technology and Research (ASTAR), Institute of Molecular and Cell Biology Singapore.
Wei-Miao YuComputational BioImage Analysis Unit, Agency of Science, Technology and Research (ASTAR), Institute of Molecular and Cell Biology Singapore.
Scott TurnerKinemed Inc. Emeryville CA.
Martien P M CaspersDepartment of Microbiology and Systems Biology Netherlands Organisation for Applied Scientific Research Zeist The Netherlands.
Ibon Martínez-ArranzOWL Metabolomics Derio Spain.
Elsbet PietermanDepartment of Metabolic Health Research Netherlands Organization for Applied Scientific Research Leiden The Netherlands.
Reinout StoopDepartment of Metabolic Health Research Netherlands Organization for Applied Scientific Research Leiden The Netherlands.
Arianne van KoppenDepartment of Metabolic Health Research Netherlands Organization for Applied Scientific Research Leiden The Netherlands.
Anita M van den HoekDepartment of Metabolic Health Research Netherlands Organization for Applied Scientific Research Leiden The Netherlands.
José M MatoCIC bioGUNE, CIBERehd Derio Spain.
Roeland HanemaaijerDepartment of Metabolic Health Research Netherlands Organization for Applied Scientific Research Leiden The Netherlands.
Cristina AlonsoOWL Metabolomics Derio Spain.
Robert KleemannDepartment of Metabolic Health Research Netherlands Organization for Applied Scientific Research Leiden The Netherlands.
Netherlands Organisation for Applied Scientific Research · NLOWL (Spain) · ESAgency for Science, Technology and Research · SGCIC bioGUNE · ESKineMed (United States) · US

Funding

Role of SAMe in Pathogenesis and Treatment of Non-Alcholic Fatty Liver DiseaseR01AT001576 · NCCIH · UNIVERSITY OF SOUTHERN CALIFORNIA · PI LU, SHELLY CHI-LOO · 2002 to 2018
$5.0M
NCCIH NIH HHS R01 AT001576
6 · The paper itself

Abstract

Concerns have been raised about whether preclinical models sufficiently mimic molecular disease processes observed in nonalcoholic steatohepatitis (NASH) patients, bringing into question their translational value in studies of therapeutic interventions in the process of NASH/fibrosis. We investigated the representation of molecular disease patterns characteristic for human NASH in high-fat diet (HFD)-fed Ldlr-/-.Leiden mice and studied the effects of obeticholic acid (OCA) on these disease profiles. Multiplatform serum metabolomic profiles and genome-wide liver transcriptome from HFD-fed Ldlr-/-.Leiden mice were compared with those of NASH patients. Mice were profiled at the stage of mild (24 weeks HFD) and severe (34 weeks HFD) fibrosis, and after OCA intervention (24-34 weeks; 10 mg/kg/day). Effects of OCA were analyzed histologically, biochemically, by immunohistochemistry, using deuterated water technology (

Identifiers

PMID30556039
PMCPMC6287481
OpenAlexW2899024699

What OpenQuestion holds

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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.