Evidence map›Paper›PMID 28914407›Full record

ArticleEndocrine2017

Association of fetuin B with markers of liver fibrosis in nonalcoholic fatty liver disease.

Thomas Ebert, Nicolas Linder, Alexander Schaudinn, Harald Busse, Joachim Berger, Ralf Lichtinghagen, Volker Keim, Johannes Wiegand, Thomas Karlas

Abstract read
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In one paragraph

Article in Endocrine, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed, 1 pooled it
1.2field-weighted citation impact, top 20% 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

7 citing papers in PubMed, 1 synthesis or guideline pooled it, 19 citations in OpenAlex.

  1. Fetuin-A and Fetuin-B in Non-Alcoholic Fatty Liver Disease: A Meta-Analysis and Meta-Regression.International journal of environmental research and public health · 2020
    Pooled it
  2. Trial
  3. Review
  4. Article
  5. Review
  6. Article
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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

9 authors at 3 institutions in 1 country.

Thomas EbertDepartment of Endocrinology and Nephrology, University of Leipzig, 04103, Leipzig, Germany. Thomas.ebert@medizin.uni-leipzig.de.ORCID http://orcid.org/0000-0003-1683-9276
Nicolas LinderLeipzig University Medical Center, IFB AdiposityDiseases, 04103, Leipzig, Germany.
Alexander SchaudinnDepartment of Diagnostic and Interventional Radiology, University Hospital Leipzig, 04103, Leipzig, Germany.
Harald BusseDepartment of Diagnostic and Interventional Radiology, University Hospital Leipzig, 04103, Leipzig, Germany.
Joachim BergerDivision of Gastroenterology and Rheumatology, University Hospital Leipzig, 04103, Leipzig, Germany.
Ralf LichtinghagenInstitute of Clinical Chemistry, Hannover Medical School, 30625, Hannover, Germany.
Volker KeimDivision of Gastroenterology and Rheumatology, University Hospital Leipzig, 04103, Leipzig, Germany.
Johannes WiegandDivision of Gastroenterology and Rheumatology, University Hospital Leipzig, 04103, Leipzig, Germany.
Thomas KarlasDivision of Gastroenterology and Rheumatology, University Hospital Leipzig, 04103, Leipzig, Germany.
University Hospital Leipzig · DELeipzig University of Applied Sciences · DEMedizinische Hochschule Hannover · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveThe liver-derived plasma protein fetuin B is associated with nonalcoholic fatty liver disease (NAFLD) and impaired glucose homeostasis in mice. However, its association with non-invasive ultrasound- and magnetic resonance (MR)-based markers of liver fibrosis and steatosis, the enhanced liver fibrosis (ELF) score, liver biopsy, as well as rs738409 in PNPLA3, has not been elucidated in NAFLD, so far. DESIGN AND

methodsThe association of circulating fetuin B and transient elastography (TE), controlled attenuation parameter (CAP),

resultsSerum fetuin B levels did not differ between NAFLD patients and controls (p = 0.863). Fetuin B was independently and negatively associated with transient elastography liver stiffness measurement (LSM) (p = 0.002), but not with the steatosis markers CAP or

conclusionsFetuin B is independently and negatively associated with non-invasive markers of liver fibrosis and PNPLA3 status in NAFLD patients but does not show a correlation with the hepatic lipid content. Future studies need to elucidate the pathophysiological significance of fetuin B in NAFLD and its potential value as predictor for disease severity.

Indexed as

AdolescentAdultAgedAllelesBiomarkersElasticity Imaging TechniquesFemaleFetuin-BHumansLiverLiver CirrhosisMagnetic Resonance SpectroscopyMaleMiddle AgedNon-alcoholic Fatty Liver DiseaseUltrasonographyBiomarkersFetuin-BAdipokineDiabetesELF scoreFetuin BHepatokineNonalcoholic fatty liver disease

Identifiers

PMID28914407
OpenAlexW2755093253

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.