Evidence map›Paper›PMID 33330965›Full record

ArticleNeuropsychiatrie : Klinik, Diagnostik, Therapie und Rehabilitation : Organ der Gesellschaft Osterreichischer Nervenarzte und Psychiater2021

Association of fibroblast growth factor 21 with alcohol consumption and alcohol liver cirrhosis.

Jolana Wagner-Skacel, Angela Horvath, Philipp Grande, Julian Wenninger, Franziska Matzer, Christian Fazekas, Sabrina Mörkl, Andreas Meinitzer, Vanessa Stadlbauer

Open access · hybridAbstract read
In one paragraph

Article in Neuropsychiatrie : Klinik, Diagnostik, Therapie und Rehabilitation : Organ der Gesellschaft Osterreichischer Nervenarzte und Psychiater, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed, 1 pooled it
1.1field-weighted citation impact, top 23% 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

9 citing papers in PubMed, 1 synthesis or guideline pooled it, 20 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. Review
  5. Article
  6. Review
  7. Article
  8. Article
  9. 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

9 authors at 1 institution in 1 country.

Jolana Wagner-SkacelDepartment of Medical Psychology and Psychotherapy, Medical University of Graz (MUG), Auenbruggerplatz 3, 8036, Graz, Austria. jolana.wagner-skacel@medunigraz.at.
Angela HorvathDivision of Gastroenterology and Hepatology, Medical University of Graz (MUG), Graz, Austria.
Philipp GrandeDivision of Gastroenterology and Hepatology, Medical University of Graz (MUG), Graz, Austria.
Julian WenningerDepartment of Child and Adolescent Psychiatry, LKH Graz II, Graz, Austria.
Franziska MatzerDepartment of Medical Psychology and Psychotherapy, Medical University of Graz (MUG), Auenbruggerplatz 3, 8036, Graz, Austria.
Christian FazekasDepartment of Medical Psychology and Psychotherapy, Medical University of Graz (MUG), Auenbruggerplatz 3, 8036, Graz, Austria.
Sabrina MörklDepartment of Psychiatry and Psychotherapeutic Medicine, Medical University of Graz (MUG), Graz, Austria.
Andreas MeinitzerDepartment of Clinical and Chemical Laboratory Diagnostics, Medical University of Graz (MUG), Graz, Austria.
Vanessa StadlbauerDivision of Gastroenterology and Hepatology, Medical University of Graz (MUG), Graz, Austria.
Medical University of Graz · AT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundFibroblast growth factor 21 (FGF21) is produced in the liver and binds to different complex receptor/coreceptor systems. Besides many other processes, FGF21 regulates the intake of simple sugars and alcohol. Increased levels of FGF21 decrease harmful alcohol intake in mice. To increase our understanding on the relationship between FGF21 and alcohol intake in humans, we aimed to measure FGF21 levels in patients with alcoholic liver cirrhosis (ALC) in comparison to patients with nonalcoholic liver cirrhosis (NALC) and healthy persons based on their present alcohol consumption.

methodsAlcohol intake was verified by urinary ethyl glucuronide (uETG) levels, eating and drinking behaviour by a Food Frequency Questionnaire and FGF 21 plasma levels were determined by ELISA in 96 persons (ALC n = 41; NALC n = 34; healthy n = 21).

resultsBoth ALC and NALC patients with elevated ETG levels (≥0.5 μg/ml; indicating alcohol consumption in the last 12-72 h) showed significantly higher FGF21 plasma levels in comparison to patients with negative ETG levels. Eating behaviour did not have an impact on FGF21 plasma levels.

conclusionsIncreased FGF21 levels in patients with recent alcohol consumption (verified by ETG) confirmed the first part of the liver-brain endocrine axis: alcohol consumption was associated with increased FGF21 levels. We could not confirm that elevated FGF21 levels were associated with reduced alcohol intake as a result. That points towards a pathology in this pathway, which might be caused by a malfunction of β‑Klotho or FGF receptors according to other studies and chronic alcohol dependency. Further research is required to clarify these pathologies, which may open new pharmacological treatment for patients with alcohol use disorder and alcohol dependence.

Indexed as

Liver Cirrhosis, AlcoholicAlcohol DrinkingAnimalsFibroblast Growth FactorsHumansLiver CirrhosisMiceFGF21 protein, humanfibroblast growth factor 21Fibroblast Growth FactorsAlcohol use disorderEnd stageFGF21Liver-brain axisLiver disease

Identifiers

PMID33330965
PMCPMC8429377
OpenAlexW3111133849

What OpenQuestion 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 OpenQuestion graph.