Evidence map›Paper›PMID 31278069›Full record

ArticleEBioMedicine2019

Obesity in acute alcoholic hepatitis increases morbidity and mortality.

Richard Parker, S J Kim, G Y Im, J Nahas, B Dhesi, N Vergis, A Sinha, A Ghezzi, M R Rink, A McCune and 5 more

Open access · goldAbstract read
In one paragraph

Article in EBioMedicine, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed, 1 pooled it
3.8field-weighted citation impact, top 6% 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

32 citing papers in PubMed, 1 synthesis or guideline pooled it, 47 citations in OpenAlex.

  1. AGA Clinical Practice Update on Bariatric Surgery in Cirrhosis: Expert Review.Clinical gastroenterology and hepatology : the official clinical practice journal of the American Gastroenterological Association · 2021
    Guideline
  2. Review
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  10. Review
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  12. [Cirrhosis recompensation: clinical complications].Zhonghua gan zang bing za zhi = Zhonghua ganzangbing zazhi = Chinese journal of hepatology · 2023
    Article
  13. Alcohol-related hepatitis: A review article.World journal of gastroenterology · 2023
    Review
  14. Review
  15. Article
  16. Review
  17. Non-alcoholic fatty liver disease and liver secretome.Archives of pharmacal research · 2022
    Review
  18. Review
  19. Article
  20. Alcohol and Metabolic-associated Fatty Liver Disease.Journal of clinical and translational hepatology · 2021
    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

15 authors at 7 institutions in 2 countries.

Richard ParkerLiver and Hepatobiliary Unit, University Hospitals Birmingham NHS Foundation Trust, Birmingham, UK; Centre for Liver Research, University of Birmingham, Birmingham, UK; National Institute for Alcoholism and Alcohol Abuse, National Institutes of Health, Rockville, MD, USA. Electronic address: richardparker@nhs.net.
S J KimNational Institute for Alcoholism and Alcohol Abuse, National Institutes of Health, Rockville, MD, USA.
G Y ImMount Sinai Medical Centre, New York, NY, USA.
J NahasMount Sinai Medical Centre, New York, NY, USA.
B DhesiLiver and Hepatobiliary Unit, University Hospitals Birmingham NHS Foundation Trust, Birmingham, UK.
N VergisImperial College Healthcare NHS Foundation Trust, UK.
A SinhaDepartment of Liver Medicine, University Hospitals Bristol NHS Foundation Trust, UK.
A GhezziNIHR Nottingham Biomedical Research Centre, Nottingham University Hospitals NHS Trust and the University Of Nottingham, Nottingham, UK.
M R RinkCentre for Liver Research, University of Birmingham, Birmingham, UK.
A McCuneDepartment of Liver Medicine, University Hospitals Bristol NHS Foundation Trust, UK.
G P AithalNIHR Nottingham Biomedical Research Centre, Nottingham University Hospitals NHS Trust and the University Of Nottingham, Nottingham, UK.
P N NewsomeLiver and Hepatobiliary Unit, University Hospitals Birmingham NHS Foundation Trust, Birmingham, UK; Centre for Liver Research, University of Birmingham, Birmingham, UK.
C J WestonCentre for Liver Research, University of Birmingham, Birmingham, UK.
A HoltLiver and Hepatobiliary Unit, University Hospitals Birmingham NHS Foundation Trust, Birmingham, UK.
B GaoNational Institute for Alcoholism and Alcohol Abuse, National Institutes of Health, Rockville, MD, USA.
National Institutes of Health · USUniversity Hospitals Birmingham NHS Foundation Trust · GBMount Sinai Medical Center · USNIHR Birmingham Liver Biomedical Research Unit · GBNottingham University Hospitals NHS Trust · GBUniversity Hospitals Bristol NHS Foundation Trust · GBImperial College Healthcare NHS Trust · GB

Funding

Pathogenesis and Novel Therapeutic Targets of Steatotic Liver Disease and CancerZIAAA000369 · NIAAA · NATIONAL INSTITUTE ON ALCOHOL ABUSE AND ALCOHOLISM · PI GAO, BIN · 2009 to 2025
$23.4M
Medical Research Council MR/N005953/1
6 · The paper itself

Abstract

backgroundAlcohol and obesity synergise to increase the risk of liver-related mortality. We examined the influence of adiposity on clinical outcomes in alcoholic hepatitis (AH) and the underlying inflammatory crosstalk between adipose tissue (AT) and the liver.

methodsA cohort of 233 patients with AH from the UK and USA provided data to analyse the effects of obesity in AH. Body mass index was corrected for the severity of ascites, termed cBMI. Inflammatory and metabolic profiling was undertaken by proteome analysis of human serum samples. The effect of alcohol on adipose tissue and CXCL11 expression was studied in 3 T3-derived adipocytes and in mice using the high-fat diet-plus-binge ethanol model.

findingsObesity was common amongst patients with AH, seen in 19% of individuals. Obesity (HR 2.22, 95%CI 1.1-4.3, p = .022) and underweight (HR 2.38, 1.00-5.6, p = .049) were independently associated with mortality at 3 months. Proteome analysis demonstrated multiple metabolic and inflammatory factors differentially expressed in obese AH verse lean AH, with CXCL11 being the most elevated factor in obese AH. In vitro analysis of cultured adipocytes and in vivo analysis of mouse models showed that alcohol induced CXCL11 expression in AT, but not in liver.

interpretationObesity is common in AH and associated with a greater than two-fold increase in short-term mortality. Obese AH is associated with a different inflammatory phenotype, with the greatest elevation in CXCL11. These data confirm that adiposity is clinically important in acute alcohol-related liver disease and illustrate the adipose-liver inflammatory axis in AH. FUND: This work was supported in part by an EASL Sheila Sherlock Physician Scientist Fellowship. The funder played no role in gathering or analysing data or writing the manuscript. This paper presents independent research supported by the NIHR Birmingham Biomedical Research Centre at the University Hospitals Birmingham NHS Foundation Trust and the University of Birmingham. The views expressed are those of the author(s) and not necessarily those of the NHS, the NIHR or the Department of Health and Social Care.

Indexed as

AdipocytesAdipose TissueAdiposityAnimalsChemokine CXCL11Cohort StudiesDiet, High-FatFemaleGene Expression RegulationHepatitis, AlcoholicHumansLiverMaleMiceMorbidityObesityChemokine CXCL11Cxcl11 protein, mouseAdiposeAlcoholic hepatitisObesity

Identifiers

PMID31278069
PMCPMC6642069
OpenAlexW2954172987

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.