Evidence map›Paper›PMID 27759439›Full record

ReviewExpert opinion on drug metabolism & toxicology2017

Drug-induced steatohepatitis.

Ajit Dash, Robert A Figler, Arun J Sanyal, Brian R Wamhoff

Registry-linked trialAbstract readReview
In one paragraph

Review in Expert opinion on drug metabolism & toxicology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT05618626 (Cardiovascular Diseases), which is not on this map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
–field-weighted citation impact
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.

NCT05618626 narecruitingnot on this mapstarted 2021, after this paper: background citation

Cardiovascular Diseases (CVD) and Nonalcoholic Fatty Liver Diseases (NAFLD) Among Gallstone and Cholecystectomy Patients and the Impact of a Novel Diet and Muscle Training Program

TypeinterventionalSponsorPontificia Universidad Catolica de ChileRan2021 to 2025Enrolled300ConditionsNon-Alcoholic Fatty Liver Disease, Gallstone DiseaseArmsPhysical exercise and dietary intervention for NAFLD
3 · Its place in the literature

Who cites it

29 citing papers in PubMed.

  1. Long-term hepatic safety of lomitapide in homozygous familial hypercholesterolaemia.Liver international : official journal of the International Association for the Study of the Liver · 2023
    Trial
  2. Trial
  3. Article
  4. Review
  5. Review
  6. Article
  7. Mechanisms of drug induced liver injury.Cellular and molecular life sciences : CMLS · 2025
    Review
  8. Review
  9. Article
  10. Article
  11. Article
  12. Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Review
  18. Review
  19. Review
  20. Review
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

4 authors.

Ajit Dasha HemoShear Therapeutics LLC , Charlottesville , VA , USA.
Robert A Figlera HemoShear Therapeutics LLC , Charlottesville , VA , USA.
Arun J Sanyalb Department of Internal Medicine, School of Medicine , Virginia Commonwealth University , Richmond , VA , USA.
Brian R Wamhoffa HemoShear Therapeutics LLC , Charlottesville , VA , USA.

Funding

Development of a human hepatocyte predictive pharmacology and toxicology system.R44DK091104 · NIDDK · HEMOSHEAR THERAPEUTICS, LLC · PI WAMHOFF, BRIAN ROBERT · 2013 to 2013
$1.6M
NIDDK NIH HHS R44 DK091104
6 · The paper itself

Abstract

introductionDrug induced steatohepatitis (DISH), a form of drug induced liver injury (DILI) is characterized by intracellular accumulation of lipids in hepatocytes and subsequent inflammatory events, in some ways similar to the pathology seen with other metabolic, viral and genetic causes of non alcoholic fatty liver disease and steatohepatitis (NAFLD and NASH). Areas covered: This paper provides a comprehensive review of the main underlying mechanisms by which various drugs cause DISH, and outlines existing preclinical tools to predict it and study underlying pathways involved. The translational hurdles of these models are discussed, with the example of an organotypic liver system designed to address them. Finally, we describe the clinical assessment and management of DISH. Expert Opinion: The complexity of the interconnected mechanistic pathways underlying DISH makes it important that preclinical evaluation of drugs is done in a physiologically and metabolically relevant context. Advanced organotypic tissue models, coupled with translational functional biomarkers and next-generational pan-omic measurements, may offer the best shot at gathering mechanistic knowledge and potential of a drug causing steatohepatitis. Ultimately this information could also help predict, detect or guide the development of specific treatments for DISH, which is an unmet need as of today.

Indexed as

AnimalsChemical and Drug Induced Liver InjuryDrug Evaluation, PreclinicalFatty LiverHepatocytesHumansLipid MetabolismModels, BiologicalDILIDrug-induced steatohepatitisliverNASHorganotypic

Identifiers

PMID27759439
PMCPMC7288748

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

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.