Evidence map›Paper›PMID 29437639›Full record

ArticleBlood advances2018

Soluble GPVI is elevated in injured patients: shedding is mediated by fibrin activation of GPVI.

Samantha J Montague, Céline Delierneux, Christelle Lecut, Nathalie Layios, Robert J Dinsdale, Christine S-M Lee, Natalie S Poulter, Robert K Andrews, Peter Hampson, Christopher M Wearn and 11 more

Open access · goldAbstract read
In one paragraph

Article in Blood advances, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
4.1field-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

25 citing papers in PubMed, 64 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Review
  5. Article
  6. GPVI inhibition: Advancing antithrombotic therapy in cardiovascular disease.European heart journal. Cardiovascular pharmacotherapy · 2024
    Review
  7. Fewer severe infections with tranexamic acid in patients with hematologic malignancies.Research and practice in thrombosis and haemostasis · 2024
    Article
  8. Article
  9. Review
  10. Fibrin reaches out to GPVI to influence how platelets shape clots.Journal of thrombosis and haemostasis : JTH · 2023
    Article
  11. An Insight into Recent Advances on Platelet Function in Health and Disease.International journal of molecular sciences · 2022
    Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. Platelet GPVI (Glycoprotein VI) and Thrombotic Complications in the Venous System.Arteriosclerosis, thrombosis, and vascular biology · 2021
    Review
  17. Role of Platelets in Detection and Regulation of Infection.Arteriosclerosis, thrombosis, and vascular biology · 2021
    Review
  18. Review
  19. Polymorphisms inInternational journal of environmental research and public health · 2020
    Article
  20. 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

21 authors at 9 institutions in 3 countries.

Samantha J MontagueInstitute of Cardiovascular Sciences, University of Birmingham, Birmingham, United Kingdom.ORCID 0000-0002-8934-3901
Céline DelierneuxGroupe Interdisciplinaire de Génoprotéomique Appliquée-Cardiovascular Sciences, University of Liège, Liège, Belgium.ORCID 0000-0003-2638-0104
Christelle LecutLaboratory of Hematology and.
Nathalie LayiosGroupe Interdisciplinaire de Génoprotéomique Appliquée-Cardiovascular Sciences, University of Liège, Liège, Belgium.
Robert J DinsdaleScar Free Foundation for Burns Research, Queen Elizabeth Hospital Birmingham, University Hospitals Birmingham National Health Service (NHS) Foundation Trust, Birmingham, United Kingdom.
Christine S-M LeeAustralian Cancer Research Foundation Department of Cancer Biology and Therapeutics, John Curtin School of Medical Research, and.ORCID 0000-0002-3851-9364
Natalie S PoulterInstitute of Cardiovascular Sciences, University of Birmingham, Birmingham, United Kingdom.ORCID 0000-0002-3187-2130
Robert K AndrewsAustralian Centre for Blood Diseases, Monash University, Melbourne, VIC, Australia.
Peter HampsonScar Free Foundation for Burns Research, Queen Elizabeth Hospital Birmingham, University Hospitals Birmingham National Health Service (NHS) Foundation Trust, Birmingham, United Kingdom.
Christopher M WearnScar Free Foundation for Burns Research, Queen Elizabeth Hospital Birmingham, University Hospitals Birmingham National Health Service (NHS) Foundation Trust, Birmingham, United Kingdom.
Nathalie MaesDepartment of Biostatics and Medico-Economic Information, University Hospital of Liège, Liège, Belgium.
Jonathan BishopNational Institute for Health Research Surgical Reconstruction and Microbiology Centre (Trauma Research), University of Birmingham, Birmingham, United Kingdom.ORCID 0000-0003-1789-5886
Amy BamfordScar Free Foundation for Burns Research, Queen Elizabeth Hospital Birmingham, University Hospitals Birmingham National Health Service (NHS) Foundation Trust, Birmingham, United Kingdom.ORCID 0000-0002-8887-484X
Chris GardinerDepartment of Haematology, University College London, London, United Kingdom; and.ORCID 0000-0002-2318-0062
Woei Ming LeeAustralian Cancer Research Foundation Department of Cancer Biology and Therapeutics, John Curtin School of Medical Research, and.
Tariq IqbalQueen Elizabeth Hospital Birmingham, University Hospitals Birmingham NHS Foundation Trust, Birmingham, United Kingdom.
Naiem MoiemenScar Free Foundation for Burns Research, Queen Elizabeth Hospital Birmingham, University Hospitals Birmingham National Health Service (NHS) Foundation Trust, Birmingham, United Kingdom.
Steve P WatsonInstitute of Cardiovascular Sciences, University of Birmingham, Birmingham, United Kingdom.ORCID 0000-0002-7846-7423
Cécile OuryGroupe Interdisciplinaire de Génoprotéomique Appliquée-Cardiovascular Sciences, University of Liège, Liège, Belgium.ORCID 0000-0002-7561-0132
Paul HarrisonScar Free Foundation for Burns Research, Queen Elizabeth Hospital Birmingham, University Hospitals Birmingham National Health Service (NHS) Foundation Trust, Birmingham, United Kingdom.ORCID 0000-0003-4610-8909
Elizabeth E GardinerAustralian Cancer Research Foundation Department of Cancer Biology and Therapeutics, John Curtin School of Medical Research, and.ORCID 0000-0001-9453-9688
National Health Service · GBUniversity of Liège · BEAustralian Cancer Research Foundation · AUAustralian National University · AUUniversity of Birmingham · GBAustralian Centre for HIV and Hepatitis Virology Research · AUNational Institute for Health Research · GBUniversity College London · GBUniversity Hospitals Birmingham NHS Foundation Trust · GB

Funding

British Heart Foundation CH/03/003/15571
6 · The paper itself

Abstract

Soluble glycoprotein VI (sGPVI) is shed from the platelet surface and is a marker of platelet activation in thrombotic conditions. We assessed sGPVI levels together with patient and clinical parameters in acute and chronic inflammatory conditions, including patients with thermal injury and inflammatory bowel disease and patients admitted to the intensive care unit (ICU) for elective cardiac surgery, trauma, acute brain injury, or prolonged ventilation. Plasma sGPVI was measured by enzyme-linked immunosorbent assay and was elevated on day 14 after thermal injury, and was higher in patients who developed sepsis. sGPVI levels were associated with sepsis, and the value for predicting sepsis was increased in combination with platelet count and Abbreviated Burn Severity Index. sGPVI levels positively correlated with levels of D-dimer (a fibrin degradation product) in ICU patients and patients with thermal injury. sGPVI levels in ICU patients at admission were significantly associated with 28- and 90-day mortality independent of platelet count. sGPVI levels in patients with thermal injury were associated with 28-day mortality at days 1, 14, and 21 when adjusting for platelet count. In both cohorts, sGPVI associations with mortality were stronger than D-dimer levels. Mechanistically, release of GPVI was triggered by exposure of platelets to polymerized fibrin, but not by engagement of G protein-coupled receptors by thrombin, adenosine 5'-diphosphate, or thromboxane mimetics. Enhanced fibrin production in these patients may therefore contribute to the observed elevated sGPVI levels. sGPVI is an important platelet-specific marker for platelet activation that predicts sepsis progression and mortality in injured patients.

Indexed as

Platelet ActivationPredictive Value of TestsBiomarkersBurnsDisease ProgressionFibrinFibrin Fibrinogen Degradation ProductsHumansInflammationInflammatory Bowel DiseasesMortalityPlatelet CountPlatelet Membrane GlycoproteinsSepsisSolubilityBiomarkersFibrinFibrin Fibrinogen Degradation Productsfibrin fragment DPlatelet Membrane Glycoproteinsplatelet membrane glycoprotein VI

Identifiers

PMID29437639
PMCPMC5812322
OpenAlexW2787382587

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.