Evidence map›Paper›PMID 30619998›Full record

ArticleHepatology communications2019

Inhibition of Triggering Receptor Expressed on Myeloid Cells 1 Ameliorates Inflammation and Macrophage and Neutrophil Activation in Alcoholic Liver Disease in Mice.

David Tornai, Istvan Furi, Zu T Shen, Alexander B Sigalov, Sahin Coban, Gyongyi Szabo

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 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
1.6field-weighted citation impact, top 16% 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, 33 citations in OpenAlex.

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  14. Emerging medical therapies for severe alcoholic hepatitis.Clinical and molecular hepatology · 2020
    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

6 authors at 2 institutions in 1 country.

David TornaiDepartment of Medicine University of Massachusetts Medical School Worcester MA.
Istvan FuriDepartment of Medicine University of Massachusetts Medical School Worcester MA.
Zu T ShenSignaBlok, Inc. Shrewsbury MA.
Alexander B SigalovSignaBlok, Inc. Shrewsbury MA.
Sahin CobanDepartment of Medicine University of Massachusetts Medical School Worcester MA.
Gyongyi SzaboDepartment of Medicine University of Massachusetts Medical School Worcester MA.
University of Massachusetts Chan Medical School · USSignaBlok (United States) · US

Funding

Alcohol and Monocyte Signaling Administrative SupplementR01AA011576 · NIAAA · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI Gyongyi Szabo · 1998 to 2026
$9.3M
Novel Therapies in alcoholic hepatitis - UMMS Translational ProgramU01AA021907 · NIAAA · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI SZABO, GYONGYI · 2012 to 2017
$2.0M
Treatment of alcoholic liver disease with novel targeted inhibitorsR43AA024355 · NIAAA · SIGNABLOK, INC. · PI SIGALOV, ALEXANDER B · 2016 to 2016
$223k
NIAAA NIH HHS R01 AA011576NIAAA NIH HHS R43 AA024355NIAAA NIH HHS U01 AA021907
6 · The paper itself

Abstract

Alcoholic liver disease (ALD) is characterized by macrophage and neutrophil leukocyte recruitment and activation in the liver. Damage- and pathogen-associated molecular patterns contribute to a self-perpetuating proinflammatory state in ALD. Triggering receptor expressed on myeloid cells 1 (TREM-1) is a surface receptor that amplifies inflammation induced by toll-like receptors (TLRs) and is expressed on neutrophils and monocytes/macrophages. We hypothesized that TREM-1 signaling contributes to proinflammatory pathway activation in ALD. Using an

Identifiers

PMID30619998
PMCPMC6312652
OpenAlexW2899248455

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.