Evidence map›Paper›PMID 30302735›Full record

ReviewHepatology international2019

Antifibrotics in liver disease: are we getting closer to clinical use?

Meena B Bansal, Naichaya Chamroonkul

Erratum issuedAbstract readReview
PubMed Publisher
In one paragraph

Review in Hepatology international, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing 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

24 citing papers in PubMed.

  1. Trial
  2. Review
  3. Article
  4. Review
  5. Review
  6. Renin-angiotensin system inhibitors and risk of hepatocellular carcinoma among patients with hepatitis B virus infection.CMAJ : Canadian Medical Association journal = journal de l'Association medicale canadienne · 2024
    Article
  7. Article
  8. Review
  9. Current investigations for liver fibrosis treatment: between repurposing the FDA-approved drugs and the other emerging approaches.Journal of pharmacy & pharmaceutical sciences : a publication of the Canadian Society for Pharmaceutical Sciences, Societe canadienne des sciences pharmaceutiques · 2023
    Review
  10. Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Fasudil prevents liver fibrosisWorld journal of gastroenterology · 2021
    Article
  17. Article
  18. Article
  19. Antihepatic Fibrosis Drugs in Clinical Trials.Journal of clinical and translational hepatology · 2020
    Review
  20. Water-Soluble Pristine CPharmaceutics · 2020
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

2 authors.

Meena B BansalDivision of Liver Diseases, Icahn School of Medicine at Mount Sinai, 1425 Madison Avenue, Box 1123, New York, NY, 10029, USA. meena.bansal@mssm.edu.
Naichaya ChamroonkulDivision of Liver Diseases, Icahn School of Medicine at Mount Sinai, 1425 Madison Avenue, Box 1123, New York, NY, 10029, USA.

Funding

HIV and hepatic inflammation and fibrosisR01DK108364 · NIDDK · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI BANSAL, MEENA B · 2015 to 2019
$1.1M
NIDDK NIH HHS R01 DK108364
6 · The paper itself

Abstract

The process of wound healing in response to chronic liver injury leads to the development of liver fibrosis. Regardless of etiology, the profound impact of the degree of liver fibrosis on the prognosis of chronic liver diseases has been well demonstrated. While disease-specific therapy, such as treatments for viral hepatitis, has been shown to reverse liver fibrosis and cirrhosis in both clinical trials and real-life practice, subsets of patients do not demonstrate fibrosis regression. Moreover, where disease-specific therapies are not available, the need for antifibrotics exists. Increased understanding into the pathogenesis of liver fibrosis sets the stage to focus on antifibrotic therapies attempting to: (1) Minimize liver injury and inflammation; (2) Inhibit liver fibrogenesis by enhancing or inhibiting target receptor-ligand interactions or intracellular signaling pathways; and (3) Promote fibrosis resolution. While no antifibrotic therapies are currently available, a number are now being evaluated in clinical trials, and their use is becoming closer to reality for select subsets of patients.

Indexed as

Adaptive ImmunityAdipokinesAmidesAngiotensin-Converting Enzyme InhibitorsAngiotensin Receptor AntagonistsAntioxidantsApoptosisCannabinoid Receptor AntagonistsCell CommunicationCell TransdifferentiationCellular SenescenceEndothelin Receptor AntagonistsEnzyme InhibitorsEpigenesis, GeneticEpithelial CellsExtracellular MatrixAdipokinesAmidesAngiotensin-Converting Enzyme InhibitorsAngiotensin Receptor AntagonistsAntioxidantsCannabinoid Receptor AntagonistsEndothelin Receptor AntagonistsEnzyme InhibitorsGalectinsIntegrinsNF-kappa BProtein Kinase InhibitorsProtein KinasesPyridinesReceptors, CannabinoidReceptors, CCRToll-Like ReceptorsTransforming Growth Factor betaY 27632Antifibrotic agentsLiver fibrosisPathogenesis

Identifiers

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.