Evidence map›Paper›PMID 29299759›Full record

ReviewHepatology international2018

Translating scientific discovery: the need for preclinical models of nonalcoholic steatohepatitis.

Abdul M Oseini, Banumathi K Cole, Danny Issa, Ryan E Feaver, Arun J Sanyal

Abstract readReview
In one paragraph

Review in Hepatology international, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing 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.

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

19 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Engineering Modular 3D Liver Culture MicroenvironmentsAdvanced nanobiomed research · 2022
    Article
  8. Review
  9. Review
  10. Article
  11. [Research progress on non-alcoholic fatty liver disease animal models].Zhonghua gan zang bing za zhi = Zhonghua ganzangbing zazhi = Chinese journal of hepatology · 2021
    Article
  12. A 3D Human Liver Model of Nonalcoholic Steatohepatitis.Journal of clinical and translational hepatology · 2020
    Article
  13. Review
  14. Article
  15. Article
  16. Article
  17. Review
  18. Review
  19. 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

5 authors.

Abdul M OseiniDivision of Gastroenterology, Department of Medicine, VCU School of Medicine, MCV Box 980341, Richmond, VA, 23298-0341, USA. abdul.oseini@vcuhealth.org.
Banumathi K ColeHemoShear Therapeutics, 501 Locust Ave, Suite 301, Charlottesville, VA, 22902, USA.
Danny IssaDivision of Gastroenterology, Department of Medicine, VCU School of Medicine, MCV Box 980341, Richmond, VA, 23298-0341, USA.
Ryan E FeaverHemoShear Therapeutics, 501 Locust Ave, Suite 301, Charlottesville, VA, 22902, USA.
Arun J SanyalDivision of Gastroenterology, Department of Medicine, VCU School of Medicine, MCV Box 980341, Richmond, VA, 23298-0341, USA.

Funding

Training Grant in Digestive Diseases and Liver DiseasesT32DK007150 · NIDDK · VIRGINIA COMMONWEALTH UNIVERSITY · PI SANYAL, ARUN J · 1986 to 2017
$4.2M
LIPIDOMICS BASED DIAGNOSTICS FOR NONALCOHOLIC STEATOHEPATITISR01DK105961 · NIDDK · VIRGINIA COMMONWEALTH UNIVERSITY · PI DENNIS, EDWARD A, SANYAL, ARUN J · 2015 to 2018
$2.8M
Validation of targets for therapeutic intervention in NASHR44DK115301 · NIDDK · HEMOSHEAR THERAPEUTICS, LLC · PI WAMHOFF, BRIAN ROBERT · 2017 to 2018
$1.9M
NIDDK NIH HHS R01 DK105961NIDDK NIH HHS R01 DK105961/DK/NIDDKNIDDK NIH HHS R44 DK115301NIDDK NIH HHS T32 DK007150
6 · The paper itself

Abstract

Non-alcoholic fatty liver disease (NAFLD) is the most common cause of chronic liver disease in the Western world, affecting about 1/3 of the US general population and remaining as a significant cause of morbidity and mortality. The hallmark of the disease is the excessive accumulation of fat within the liver cells (hepatocytes), which eventually paves the way to cellular stress, injury and apoptosis. NAFLD is strongly associated with components of the metabolic syndrome and is fast emerging as a leading cause of liver transplant in the USA. Based on clinico-pathologic classification, NAFLD may present as isolated lipid collection (steatosis) within the hepatocytes (referred to as non-alcoholic fatty liver; NAFL); or as the more aggressive phenotype (known as non-alcoholic steatohepatitis; NASH). There are currently no regulatory agency- approved medication for NAFLD, despite the enormous work and resources that have gone into the study of this condition. Therefore, there remains a huge unmet need in developing and utilizing pre-clinical models that will recapitulate the disease condition in humans. In line with progress being made in developing appropriate disease models, this review highlights the cutting-edge preclinical in vitro and animal models that try to recapitulate the human disease pathophysiology and/or clinical manifestations.

Indexed as

Disease Models, AnimalAnimalsDisease ProgressionHumansNon-alcoholic Fatty Liver DiseaseDiet induced animal model of non-alcoholic fatty liver disease (DIAMOND)Farnesoid X receptor (FXR)Lipitoxic systemNon-alcoholic fatty liver disease (NAFLD)Non-alcoholic steatohepatitis (NASH)Organotypic liver system

Identifiers

PMID29299759
PMCPMC5815925

What Socratic holds

Textmetadata
LicenceTDM
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 Socratic graph.