Evidence map›Paper›PMID 31516268›Full record

ReviewJournal of clinical and experimental hepatology

Drug Development for Nonalcoholic Fatty Liver Disease: Landscape and Challenges.

Prarthana Thiagarajan, Guruprasad P Aithal

Open access · greenAbstract readReview
In one paragraph

Review in Journal of clinical and experimental hepatology. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
3.5field-weighted citation impact, top 7% 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

22 citing papers in PubMed, 32 citations in OpenAlex.

  1. Review
  2. Prognostic Value of the TLM3 Biomarker Panel for Early Fibrosis Development in MASLD Within the General Population.Liver international : official journal of the International Association for the Study of the Liver · 2025
    Article
  3. Therapeutic Strategies for MASH: An Update on Drug Candidates Under Investigation in Late-Phase Clinical Trials.International journal of translational medicine (Basel, Switzerland) · 2025
    Article
  4. Challenges ofFrontiers in cell and developmental biology · 2025
    Review
  5. Review
  6. Article
  7. Review
  8. Article
  9. CSAD Ameliorates Lipid Accumulation in High-Fat Diet-Fed Mice.International journal of molecular sciences · 2022
    Article
  10. Article
  11. Review
  12. Review
  13. Review
  14. Lean NAFLD: an underrecognized and challenging disorder in medicine.Reviews in endocrine & metabolic disorders · 2021
    Review
  15. Article
  16. Article
  17. Carbon tetrachloride (CClBMC gastroenterology · 2020
    Article
  18. Ethyl Acetate Fraction ofNutrients · 2020
    Article
  19. Review
  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

2 authors at 1 institution in 1 country.

Prarthana ThiagarajanNIHR Nottingham Biomedical Research Centre, Nottingham University Hospitals NHS Trust and University of Nottingham, Nottingham, United Kingdom.
Guruprasad P AithalNIHR Nottingham Biomedical Research Centre, Nottingham University Hospitals NHS Trust and University of Nottingham, Nottingham, United Kingdom.
Nottingham University Hospitals NHS Trust · GB

Funding

Medical Research Council MR/N005953/1
6 · The paper itself

Abstract

Nonalcoholic fatty liver disease (NAFLD) is now the leading cause of chronic liver disease in industrialized economies. With no licensed treatment currently available, together with a growing prevalence that parallels global increases in obesity and type 2 diabetes, NAFLD will dominate the landscape of hepatology for the foreseeable future. A multifaceted etiopathogenesis, paucity of reproducible preclinical models that effectively recreate human NAFLD, and lack of robust surrogate trial endpoints have presented major hurdles in drug discovery and development. Smooth collaboration between bench scientists, biotechnology, pharmaceutical industries, and clinicians will be pivotal to target identification, development of effective therapies, biomarker discovery, and ultimately to bring pipeline drugs to market. This review examines the key challenges remaining in NAFLD drug development, outlines early and late phase clinical trials of candidate treatments, and discusses the journey toward biomarker discovery which may facilitate development of novel endpoints in NAFLD clinical trials, enabling meaningful response to be determined noninvasively.

Indexed as

BMI, Body Mass IndexDGAT, Diacyl Glycerol Acyl TransferaseELF, Extended Liver Fibrosis PanelendpointsFIB-4, Fibrosis 4FXR, Farnesoid X ReceptorHbA1C, Hemoglobin A1CHCC, Hepatocellular CarcinomaHOMA-IR, Homeostasis Model Assessment of Insulin ResistanceHVPG, Hepatic Venous Pressure GradientMCD, Methionine-Choline–Deficient DietMRE, MR ElastographyMRI, Magnetic Resonance ImagingMRS, Magnetic Resonance SpectroscopyNAFLDNAFLD, Nonalcoholic Fatty Liver DiseaseNASH, Nonalcoholic SteatohepatitisOCA, Obeticholic AcidOGTT, Oral Glucose Tolerance Testpreclinical modelsPro-C3, Pro-collagen 3targetsTE, Transient Elastographytherapeutics

Identifiers

PMID31516268
PMCPMC6728526
OpenAlexW2920970708

What OpenQuestion holds

Textmetadata
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.