Evidence map›Paper›PMID 31960587›Full record

ArticleLiver international : official journal of the International Association for the Study of the Liver2020

The endothelial function biomarker soluble E-selectin is associated with nonalcoholic fatty liver disease.

Nynke Simons, Mitchell Bijnen, Kristiaan A M Wouters, Sander S Rensen, Joline W J Beulens, Marleen M J van Greevenbroek, Leen M 't Hart, Jan Willem M Greve, Carla J H van der Kallen, Nicolaas C Schaper and 3 more

Open access · hybridAbstract read
In one paragraph

Article in Liver international : official journal of the International Association for the Study of the Liver, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed, 1 pooled it
2.8field-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

18 citing papers in PubMed, 1 synthesis or guideline pooled it, 38 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Article
  4. Article
  5. Article
  6. Article
  7. Prediagnostic plasma proteomics profile for hepatocellular carcinoma.Journal of the National Cancer Institute · 2024
    Article
  8. Article
  9. Article
  10. Review
  11. E-selectin in vascular pathophysiology.Frontiers in immunology · 2024
    Review
  12. Review
  13. Review
  14. Article
  15. Article
  16. Article
  17. Nutrients · 2021
    Article
  18. The endothelial function biomarker soluble E-selectin is associated with nonalcoholic fatty liver disease.Liver international : official journal of the International Association for the Study of the Liver · 2020
    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

13 authors at 4 institutions in 1 country.

Nynke SimonsDepartment of Internal Medicine, Division of Endocrinology and Metabolic Diseases, Maastricht University Medical Center, Maastricht, The Netherlands.ORCID 0000-0001-6259-8958
Mitchell BijnenDepartment of Internal Medicine, Division of General Internal Medicine, Laboratory for Metabolism and Vascular Medicine, Maastricht University Medical Center, Maastricht, The Netherlands.ORCID 0000-0003-2781-8702
Kristiaan A M WoutersDepartment of Internal Medicine, Division of General Internal Medicine, Laboratory for Metabolism and Vascular Medicine, Maastricht University Medical Center, Maastricht, The Netherlands.ORCID 0000-0001-7127-6950
Sander S RensenDepartment of General Surgery, Maastricht University Medical Center, Maastricht, The Netherlands.ORCID 0000-0001-5054-8400
Joline W J BeulensDepartment of Epidemiology and Biostatistics, Amsterdam University Medical Center - location VUmc, the Amsterdam Public Health Research Institute Amsterdam, Amsterdam, The Netherlands.ORCID 0000-0002-4181-0937
Marleen M J van GreevenbroekDepartment of Internal Medicine, Division of General Internal Medicine, Laboratory for Metabolism and Vascular Medicine, Maastricht University Medical Center, Maastricht, The Netherlands.ORCID 0000-0002-2989-1631
Leen M 't HartDepartment of Epidemiology and Biostatistics, Amsterdam University Medical Center - location VUmc, the Amsterdam Public Health Research Institute Amsterdam, Amsterdam, The Netherlands.ORCID 0000-0003-4401-2938
Jan Willem M GreveDepartment of General Surgery, Maastricht University Medical Center, Maastricht, The Netherlands.ORCID 0000-0002-8202-7076
Carla J H van der KallenDepartment of Internal Medicine, Division of General Internal Medicine, Laboratory for Metabolism and Vascular Medicine, Maastricht University Medical Center, Maastricht, The Netherlands.ORCID 0000-0003-1468-8793
Nicolaas C SchaperDepartment of Internal Medicine, Division of Endocrinology and Metabolic Diseases, Maastricht University Medical Center, Maastricht, The Netherlands.ORCID 0000-0002-2128-8029
Casper G SchalkwijkDepartment of Internal Medicine, Division of General Internal Medicine, Laboratory for Metabolism and Vascular Medicine, Maastricht University Medical Center, Maastricht, The Netherlands.ORCID 0000-0003-0190-2690
Coen D A StehouwerDepartment of Internal Medicine, Division of General Internal Medicine, Laboratory for Metabolism and Vascular Medicine, Maastricht University Medical Center, Maastricht, The Netherlands.ORCID 0000-0001-8752-3223
Martijn C G J BrouwersDepartment of Internal Medicine, Division of Endocrinology and Metabolic Diseases, Maastricht University Medical Center, Maastricht, The Netherlands.ORCID 0000-0002-8229-3331
Maastricht University Medical Centre · NLMaastricht University · NLLeiden University Medical Center · NLUniversity Medical Center Utrecht · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND &

aimsPlasma soluble E-selectin (sE-selectin) is a frequently used biomarker of systemic endothelial dysfunction. The present study explored the relationship between nonalcoholic fatty liver disease (NAFLD) and plasma sE-selectin levels.

methodsExpression of E-selectin in liver, visceral adipose tissue (VAT) and muscle was studied in relation to plasma sE-selectin in severely obese individuals (n = 74). The course of hepatic E-selectin expression in relation to hepatic steatosis and inflammation was examined in C57BL/6J LDLR

resultsE-selectin expression in liver, not VAT or muscle, was associated with plasma sE-selectin in severely obese individuals (β = 0.26; 95% CI: 0.05-0.47). NAFLD severity was associated with hepatic E-selectin expression (P = .02) and plasma sE-selectin (P = .003). LDLR

conclusionsNAFLD and related markers are associated with higher expression of hepatic E-selectin and higher levels of plasma sE-selectin. Further studies are required to investigate the role of E-selectin in the pathogenesis of NAFLD and the applicability of sE-selectin as a plasma biomarker of NAFLD/NASH.

Indexed as

Non-alcoholic Fatty Liver DiseaseAcyltransferasesAdaptor Proteins, Signal TransducingAnimalsBiomarkersCadherinsLipaseLiverMiceMice, Inbred C57BLPhospholipases A2, Calcium-IndependentAcyltransferasesAdaptor Proteins, Signal TransducingBiomarkersCadherinsCdh1 protein, mouseGckr protein, mouseLipasePhospholipases A2, Calcium-IndependentPNPLA3 protein, mouseendotheliumE-selectingenetic epidemiologynonalcoholic fatty liver diseasetranslational research

Identifiers

PMID31960587
PMCPMC7317803
OpenAlexW3002707052

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.