Evidence map›Paper›PMID 27757953›Full record

ReviewThe Journal of pathology2017

Animal models of non-alcoholic fatty liver disease: current perspectives and recent advances.

Jennie Ka Ching Lau, Xiang Zhang, Jun Yu

Open access · hybridAbstract readReview
In one paragraph

Review in The Journal of pathology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 203 papers.

0numbers the graph read from it
0cells of the map it votes in
203citing papers in PubMed
25.3field-weighted citation impact, top 1% 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

203 citing papers in PubMed, 358 citations in OpenAlex.

  1. Precision pathophysiology in steatotic liver disease.Clinical and molecular hepatology · 2026
    Review
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  13. MAFLD: a ferroptotic disease.Trends in molecular medicine · 2026
    Review
  14. Article
  15. Review
  16. Loss of Mtarc1 Protects Against Steatotic Liver Disease in Mice.Liver international : official journal of the International Association for the Study of the Liver · 2026
    Article
  17. Article
  18. Article
  19. Article
  20. Article

143 more citing papers are in PubMed but not listed here.

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

3 authors at 1 institution in 1 country.

Jennie Ka Ching LauInstitute of Digestive Disease and the Department of Medicine and Therapeutics, The Chinese University of Hong Kong, Hong Kong, PR China.
Xiang ZhangInstitute of Digestive Disease and the Department of Medicine and Therapeutics, The Chinese University of Hong Kong, Hong Kong, PR China.
Jun YuInstitute of Digestive Disease and the Department of Medicine and Therapeutics, The Chinese University of Hong Kong, Hong Kong, PR China.
Chinese University of Hong Kong · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Non-alcoholic fatty liver disease (NAFLD) is a continuous spectrum of diseases characterized by excessive lipid accumulation in hepatocytes. NAFLD progresses from simple liver steatosis to non-alcoholic steatohepatitis and, in more severe cases, to liver fibrosis, cirrhosis, and hepatocellular carcinoma (HCC). Because of its growing worldwide prevalence, various animal models that mirror both the histopathology and the pathophysiology of each stage of human NAFLD have been developed. The selection of appropriate animal models continues to be one of the key questions faced in this field. This review presents a critical analysis of the histopathology and pathogenesis of NAFLD, the most frequently used and recently developed animal models for each stage of NAFLD and NAFLD-induced HCC, the main mechanisms involved in the experimental pathogenesis of NAFLD in different animal models, and a brief summary of recent therapeutic targets found by the use of animal models. Integrating the data from human disease with those from animal studies indicates that, although current animal models provide critical guidance in understanding specific stages of NAFLD pathogenesis and progression, further research is necessary to develop more accurate models that better mimic the disease spectrum, in order to provide both increased mechanistic understanding and identification/testing of novel therapeutic approaches. © 2016 The Authors. The Journal of Pathology published by John Wiley & Sons Ltd on behalf of Pathological Society of Great Britain and Ireland.

Indexed as

AnimalsCarcinoma, HepatocellularCytokinesDietDisease Models, AnimalDisease ProgressionGenetic Predisposition to DiseaseHumansLiver NeoplasmsNon-alcoholic Fatty Liver DiseaseOxidative StressCytokinesanimal modeldisease histopathologyhepatocellular carcinomanon-alcoholic fatty liver disease (NAFLD)non-alcoholic steatohepatitis

Identifiers

PMID27757953
PMCPMC5215469
OpenAlexW2532614692

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.