Evidence map›Paper›PMID 27435327›Full record

ReviewDigestive diseases and sciences2016

Targeting Hepatic Fibrosis in Autoimmune Hepatitis.

Aldo J Montano-Loza, Ragesh B Thandassery, Albert J Czaja

Abstract readReview
PubMed Publisher
In one paragraph

Review in Digestive diseases and sciences, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed, 1 pooled it
3.8field-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

13 citing papers in PubMed, 1 synthesis or guideline pooled it, 33 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Autoimmune Hepatitis and Fibrosis.Journal of clinical medicine · 2023
    Review
  4. Review
  5. Review
  6. Efficacy and safety of anti-hepatic fibrosis drugs.World journal of gastroenterology · 2020
    Review
  7. Article
  8. Article
  9. Review
  10. Article
  11. Observational
  12. Review
  13. Evolution of correlation betweenExperimental and therapeutic medicine · 2017
    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

3 authors at 3 institutions in 2 countries.

Aldo J Montano-LozaDivision of Gastroenterology and Liver Unit, University of Alberta Hospital, Edmonton, AB, Canada.
Ragesh B ThandasseryDivision of Gastroenterology and Liver Unit, University of Alberta Hospital, Edmonton, AB, Canada.
Albert J CzajaProfessor Emeritus of Medicine, Division of Gastroenterology and Hepatology, Mayo Clinic College of Medicine, 200 First Street S.W., Rochester, MN, 55905, USA. czaja.albert@mayo.edu.
Alberta Hospital Edmonton · CAMayo Clinic · USUniversity of Alberta Hospital · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hepatic fibrosis develops or progresses in 25 % of patients with autoimmune hepatitis despite corticosteroid therapy. Current management regimens lack reliable noninvasive methods to assess changes in hepatic fibrosis and interventions that disrupt fibrotic pathways. The goals of this review are to indicate promising noninvasive methods to monitor hepatic fibrosis in autoimmune hepatitis and identify anti-fibrotic interventions that warrant evaluation. Laboratory methods can differentiate cirrhosis from non-cirrhosis, but their accuracy in distinguishing changes in histological stage is uncertain. Radiological methods include transient elastography, acoustic radiation force impulse imaging, and magnetic resonance elastography. Methods based on ultrasonography are comparable in detecting advanced fibrosis and cirrhosis, but their performances may be compromised by hepatic inflammation and obesity. Magnetic resonance elastography has excellent performance parameters for all histological stages in diverse liver diseases, is uninfluenced by inflammatory activity or body habitus, has been superior to other radiological methods in nonalcoholic fatty liver disease, and may emerge as the preferred instrument to evaluate fibrosis in autoimmune hepatitis. Promising anti-fibrotic interventions are site- and organelle-specific agents, especially inhibitors of nicotinamide adenine dinucleotide phosphate oxidases, transforming growth factor beta, inducible nitric oxide synthase, lysyl oxidases, and C-C chemokine receptors types 2 and 5. Autoimmune hepatitis has a pro-fibrotic propensity, and noninvasive radiological methods, especially magnetic resonance elastography, and site- and organelle-specific interventions, especially selective antioxidants and inhibitors of collagen cross-linkage, may emerge to strengthen current management strategies.

Indexed as

Adrenal Cortex HormonesAntioxidantsApoptosisCCR5 Receptor AntagonistsCytokinesElasticity Imaging TechniquesExtracellular MatrixHepatitis, AutoimmuneHumansInflammationLiver CirrhosisMagnetic Resonance ImagingNADPH OxidasesNitric Oxide Synthase Type IIOxidative StressProtein-Lysine 6-OxidaseAdrenal Cortex HormonesAntioxidantsCCR5 Receptor AntagonistsCytokinesNADPH OxidasesNitric Oxide Synthase Type IIProtein-Lysine 6-OxidaseReceptors, CCR2Transforming Growth Factor betaAnti-fibrotic interventionsAssessmentsAutoimmune hepatitisFibrosis

Identifiers

PMID27435327
OpenAlexW2480168376

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.