Evidence map›Paper›PMID 28134813›Full record

ReviewBiomolecules2017

Key Events Participating in the Pathogenesis of  Alcoholic Liver Disease.

Fernando Magdaleno, Chuck C Blajszczak, Natalia Nieto

Open access · goldAbstract readReview
In one paragraph

Review in Biomolecules, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed, 1 pooled it
6.9field-weighted citation impact, top 2% 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, 1 synthesis or guideline pooled it, 73 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Article
  4. Review
  5. Review
  6. Review
  7. Review
  8. Review
  9. Quantitative imaging in medicine and surgery · 2023
    Article
  10. Association of promoter methylation status of NRF2 and PNPLA3 genes in alcoholic liver disease.Indian journal of gastroenterology : official journal of the Indian Society of Gastroenterology · 2022
    Article
  11. Review
  12. Article
  13. Article
  14. Review
  15. [Effect of pyroptosis in the pathogenesis of alcoholic liver disease].Zhonghua gan zang bing za zhi = Zhonghua ganzangbing zazhi = Chinese journal of hepatology · 2020
    Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. A Compound of Chinese Herbs Protects against Alcoholic Liver Fibrosis in Rats via the TGF-Evidence-based complementary and alternative medicine : eCAM · 2019
    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 1 institution in 1 country.

Fernando MagdalenoDepartment of Pathology, University of Illinois at Chicago, 840 S. Wood St., Suite 130 CSN, MC 847, Chicago, IL 60612, USA. fmverduz@uic.edu.
Chuck C BlajszczakDepartment of Pathology, University of Illinois at Chicago, 840 S. Wood St., Suite 130 CSN, MC 847, Chicago, IL 60612, USA. cblajs2@uic.edu.
Natalia NietoDepartment of Pathology, University of Illinois at Chicago, 840 S. Wood St., Suite 130 CSN, MC 847, Chicago, IL 60612, USA. nnieto@uic.edu.
University of Illinois Chicago · US

Funding

Project 2P20AA017067 · NIAAA · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI FRIEDMAN, SCOTT L. · 2008 to 2012
$2.5M
Milk osteopontin, a nutritional therapeutic intervention for alcoholic hepatitisU01AA021887 · NIAAA · UNIVERSITY OF ILLINOIS AT CHICAGO · PI NIETO, NATALIA · 2012 to 2017
$2.0M
Communication between Kupffer cells and stellate cellsR01DK069286 · NIDDK · MOUNT SINAI SCHOOL OF MEDICINE OF NYU · PI NIETO, NATALIA · 2005 to 2009
$1.2M
Osteopontin and the fibrogenic response to liver injuryR56DK069286 · NIDDK · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI NIETO, NATALIA · 2010 to 2012
$544k
NIAAA NIH HHS P20 AA017067NIAAA NIH HHS U01 AA021887NIDDK NIH HHS R01 DK069286NIDDK NIH HHS R56 DK069286
6 · The paper itself

Abstract

Alcoholic liver disease (ALD) is a leading cause of morbidity and mortality worldwide. It ranges from fatty liver to steatohepatitis, fibrosis, cirrhosis and hepatocellular carcinoma.The most prevalent forms of ALD are alcoholic fatty liver, alcoholic hepatitis (AH) and alcoholic cirrhosis, which frequently progress as people continue drinking. ALD refers to a number of symptoms/deficits that contribute to liver injury. These include steatosis, inflammation, fibrosis and cirrhosis, which, when taken together, sequentially or simultaneously lead to significant disease progression. The pathogenesis of ALD, influenced by host and environmental factors, is currentlyonly partially understood. To date, lipopolysaccharide (LPS) translocation from the gut to the portal blood, aging, gender, increased infiltration and activation of neutrophils and bone marrow-derived macrophages along with alcohol plus iron metabolism, with its associated increase in reactive oxygen species (ROS), are all key events contributing to the pathogenesis of ALD. This review aimsto introduce the reader to the concept of alcohol-mediated liver damage and the mechanisms driving injury.

Indexed as

AgingAlarminsAnimalsHumansInflammasomesLipid PeroxidationLiver Diseases, AlcoholicReactive Oxygen SpeciesAlarminsInflammasomesReactive Oxygen Speciesdamage‐associated  molecular  patternsinflammasomeironlipid  peroxidationmacrophagesneutrophilspathogen‐associated molecular patterns

Identifiers

PMID28134813
PMCPMC5372721
OpenAlexW2580400995

What Socratic holds

Textmetadata
LicenceCC BY
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 Socratic graph.