Evidence map›Paper›PMID 26909225›Full record

ArticleWorld journal of gastrointestinal pathophysiology2016

Adipose tissue-liver axis in alcoholic liver disease.

Zhi-Gang Wang, Xiao-Bing Dou, Zhan-Xiang Zhou, Zhen-Yuan Song

Open access · diamondAbstract read
In one paragraph

Article in World journal of gastrointestinal pathophysiology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
3.1field-weighted citation impact, top 9% 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

24 citing papers in PubMed, 33 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Review
  5. Article
  6. Review
  7. Heliyon · 2024
    Article
  8. Article
  9. Article
  10. Article
  11. Review
  12. Alcohol-Related Liver Disease: Basic Mechanisms and Clinical Perspectives.International journal of molecular sciences · 2021
    Review
  13. Article
  14. Article
  15. Review
  16. Effects ofMolecules (Basel, Switzerland) · 2019
    Article
  17. Article
  18. Nutritional status in patients with liver cirrhosis.Clinical and experimental hepatology · 2019
    Article
  19. Genetic and Epigenetic Modifiers of Alcoholic Liver Disease.International journal of molecular sciences · 2018
    Review
  20. Review
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

4 authors at 1 institution in 2 countries.

Zhi-Gang WangZhi-Gang Wang, College of Medical Laboratory Science and Technology, Harbin Medical University at Daqing, Daqing 163319, Heilongjiang Province, China.
Xiao-Bing DouZhi-Gang Wang, College of Medical Laboratory Science and Technology, Harbin Medical University at Daqing, Daqing 163319, Heilongjiang Province, China.
Zhan-Xiang ZhouZhi-Gang Wang, College of Medical Laboratory Science and Technology, Harbin Medical University at Daqing, Daqing 163319, Heilongjiang Province, China.
Zhen-Yuan SongZhi-Gang Wang, College of Medical Laboratory Science and Technology, Harbin Medical University at Daqing, Daqing 163319, Heilongjiang Province, China.
University of North Carolina at Greensboro · US

Funding

Homocysteine, Adiponectin, and Alcoholic Liver DiseaseR01AA017442 · NIAAA · UNIVERSITY OF ILLINOIS AT CHICAGO · PI SONG, ZHENYUAN · 2009 to 2013
$1.4M
NIAAA NIH HHS R01 AA017442
6 · The paper itself

Abstract

Alcoholic liver disease (ALD) remains an important health problem worldwide. The disease spectrum is featured by early steatosis, steatohepatitis (steatosis with inflammatory cells infiltration and necrosis), with some individuals ultimately progressing to fibrosis/cirrhosis. Although the disease progression is well characterized, no effective therapies are currently available for the treatment in humans. The mechanisms underlying the initiation and progression of ALD are multifactorial and complex. Emerging evidence supports that adipose tissue dysfunction contributes to the pathogenesis of ALD. In the first part of this review, we discuss the mechanisms whereby chronic alcohol exposure contributed to adipose tissue dysfunction, including cell death, inflammation and insulin resistance. It has been long known that aberrant hepatic methionine metabolism is a major metabolic abnormality induced by chronic alcohol exposure and plays an etiological role in the pathogenesis of ALD. The recent studies in our group documented the similar metabolic effect of chronic alcohol drinking on methionine in adipose tissue. In the second part of this review, we also briefly discuss the recent research progress in the field with a focus on how abnormal methionine metabolism in adipose tissue contributes to adipose tissue dysfunction and liver damage.

Indexed as

AdiposeAlcoholLipolysisLiverMethionineMethylation

Identifiers

PMID26909225
PMCPMC4753183
OpenAlexW2277500289

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.