Evidence map›Paper›PMID 31304452›Full record

ArticleHepatology communications2019

Emricasan Ameliorates Portal Hypertension and Liver Fibrosis in Cirrhotic Rats Through a Hepatocyte-Mediated Paracrine Mechanism.

Jordi Gracia-Sancho, Nicolò Manicardi, Martí Ortega-Ribera, Raquel Maeso-Díaz, Sergi Guixé-Muntet, Anabel Fernández-Iglesias, Diana Hide, Héctor García-Calderó, Zoe Boyer-Díaz, Patricia C Contreras and 2 more

Open access · goldAbstract read
In one paragraph

Article in Hepatology communications, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed, 2 pooled it
4.8field-weighted citation impact, top 4% 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

43 citing papers in PubMed, 2 syntheses or guidelines pooled it, 63 citations in OpenAlex.

  1. Pooled it
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  6. Article
  7. Caspase-1 in cancer and inflammatory diseases: a potential therapeutic target.Apoptosis : an international journal on programmed cell death · 2026
    Review
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  14. Sinusoidal communication in chronic liver disease.Clinical and molecular hepatology · 2025
    Review
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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

12 authors at 4 institutions in 3 countries.

Jordi Gracia-SanchoLiver Vascular Biology Research Group Barcelona Hepatic Hemodynamic Lab, IDIBAPS Biomedical Research Institute Barcelona Spain.
Nicolò ManicardiLiver Vascular Biology Research Group Barcelona Hepatic Hemodynamic Lab, IDIBAPS Biomedical Research Institute Barcelona Spain.
Martí Ortega-RiberaLiver Vascular Biology Research Group Barcelona Hepatic Hemodynamic Lab, IDIBAPS Biomedical Research Institute Barcelona Spain.
Raquel Maeso-DíazLiver Vascular Biology Research Group Barcelona Hepatic Hemodynamic Lab, IDIBAPS Biomedical Research Institute Barcelona Spain.
Sergi Guixé-MuntetLiver Vascular Biology Research Group Barcelona Hepatic Hemodynamic Lab, IDIBAPS Biomedical Research Institute Barcelona Spain.
Anabel Fernández-IglesiasLiver Vascular Biology Research Group Barcelona Hepatic Hemodynamic Lab, IDIBAPS Biomedical Research Institute Barcelona Spain.
Diana HideLiver Vascular Biology Research Group Barcelona Hepatic Hemodynamic Lab, IDIBAPS Biomedical Research Institute Barcelona Spain.
Héctor García-CalderóLiver Vascular Biology Research Group Barcelona Hepatic Hemodynamic Lab, IDIBAPS Biomedical Research Institute Barcelona Spain.
Zoe Boyer-DíazBarcelona Liver Bioservices Barcelona Spain.
Patricia C ContrerasConatus Pharmaceuticals San Diego CA.
Alfred SpadaConatus Pharmaceuticals San Diego CA.
Jaime BoschLiver Vascular Biology Research Group Barcelona Hepatic Hemodynamic Lab, IDIBAPS Biomedical Research Institute Barcelona Spain.
Centro de Investigación Biomédica en Red · ESConsorci Institut D'Investigacions Biomediques August Pi I Sunyer · ESConatus Pharmaceuticals (United States) · USUniversity Hospital of Bern · CH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In cirrhosis, liver microvascular dysfunction is a key factor increasing hepatic vascular resistance to portal blood flow, which leads to portal hypertension. De-regulated inflammatory and pro-apoptotic processes due to chronic injury play important roles in the dysfunction of liver sinusoidal cells. The present study aimed at characterizing the effects of the pan-caspase inhibitor emricasan on systemic and hepatic hemodynamics, hepatic cells phenotype, and underlying mechanisms in preclinical models of advanced chronic liver disease. We investigated the effects of 7-day emricasan on hepatic and systemic hemodynamics, liver function, hepatic microcirculatory function, inflammation, fibrosis, hepatic cells phenotype, and paracrine interactions in rats with advanced cirrhosis due to chronic CCl

Identifiers

PMID31304452
PMCPMC6601324
OpenAlexW2938297907

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.