Evidence map›Paper›PMID 29729196›Full record

ReviewHepatology (Baltimore, Md.)2018

Potential Clinical Targets in Hepatopulmonary Syndrome: Lessons From Experimental Models.

Sarah Raevens, Michael B Fallon

Abstract readReview
In one paragraph

Review in Hepatology (Baltimore, Md.), 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
2.4field-weighted citation impact, top 10% 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

23 citing papers in PubMed, 56 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Review
  6. Article
  7. Article
  8. Hepatopulmonary Syndrome, Another Face of Dysregulated BMP9 Signaling.American journal of respiratory and critical care medicine · 2024
    Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Hepatopulmonary syndrome.JHEP reports : innovation in hepatology · 2022
    Review
  14. Review
  15. Review
  16. Review
  17. Review
  18. Review
  19. Bubble Trouble in COVID-19.American journal of respiratory and critical care medicine · 2020
    Article
  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 2 institutions in 2 countries.

Sarah RaevensDepartment of Gastroenterology and Hepatology, Hepatology Research Unit, Ghent University, Ghent University Hospital, Ghent, Belgium.
Michael B FallonDepartment of Internal Medicine, University of Arizona College of Medicine, Phoenix, AZ.
Ghent University Hospital · BEUniversity of Arizona · US

Funding

Sorafenib for Hepatopulmonary SyndromeUM1HL116886 · NHLBI · UNIVERSITY OF PENNSYLVANIA · PI FALLON, MICHAEL B, KAWUT, STEVEN M · 2013 to 2015
$5.1M
Estrogen signaling in portopulmonary hypertensionR01HL113988 · NHLBI · UNIVERSITY OF PENNSYLVANIA · PI FALLON, MICHAEL TODD, KAWUT, STEVEN M · 2012 to 2016
$3.8M
MEDIATORS OF PULMONARY VASODILATATION IN LIVER DISEASER01DK056804 · NIDDK · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI FALLON, MICHAEL B · 2000 to 2013
$3.6M
Hepatopulmonary Syndrome Investigative GroupR03DK065958 · NIDDK · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI FALLON, MICHAEL B · 2004 to 2005
$290k
NHLBI NIH HHS R01 HL113988NHLBI NIH HHS UM1 HL116886NIDDK NIH HHS R01 DK056804NIDDK NIH HHS R03 DK065958
6 · The paper itself

Abstract

Hepatopulmonary syndrome (HPS) is a relatively common and potentially severe pulmonary complication of cirrhosis with increased risk of mortality. In experimental models, a complex interaction between pulmonary endothelial cells, monocytes, and the respiratory epithelium, which produces chemokines, cytokines, and angiogenic growth factors, causes alterations in the alveolar microvasculature, resulting in impaired oxygenation. Model systems are critical for evaluating mechanisms and for preclinical testing in HPS, due to the challenges of evaluating the lung in the setting of advanced liver disease in humans. This review provides an overview of current knowledge and recent findings in the rodent common bile duct ligation model of HPS, which recapitulates many features of human disease. We focus on the concepts of endothelial derangement, monocyte infiltration, angiogenesis, and alveolar type II cell dysfunction as main contributors and potential targets for therapy.

Indexed as

AnimalsDisease Models, AnimalEndothelial CellsHepatopulmonary SyndromeHumansLiverLungMiceMonocytesNeovascularization, PathologicRats

Identifiers

PMID29729196
PMCPMC6204081
OpenAlexW2799671697

What OpenQuestion 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 OpenQuestion graph.