Evidence map›Paper›PMID 39796151›Full record

ArticleInternational journal of molecular sciences2024

Assessment of Hypercoagulability in Splanchnic Vein Thrombosis by Measurement of the Hemostasis Enzymes Thrombin and Activated Protein C.

Sara Reda, Johannes Chang, Johanna Busse, Nadine Schwarz, Hannah L McRae, Jens Müller, Christian P Strassburg, Johannes Oldenburg, Bernd Pötzsch, Christian Jansen and 1 more

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
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

5 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Special Issue "Advances in Coagulation and Anticoagulation".International journal of molecular sciences · 2025
    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

11 authors.

Sara RedaInstitute of Experimental Hematology and Transfusion Medicine, University Hospital Bonn, 53127 Bonn, Germany.ORCID 0009-0006-2650-4356
Johannes ChangDepartment of Internal Medicine I, University Hospital Bonn, 53127 Bonn, Germany.ORCID 0000-0001-9635-8901
Johanna BusseInstitute of Experimental Hematology and Transfusion Medicine, University Hospital Bonn, 53127 Bonn, Germany.
Nadine SchwarzInstitute of Experimental Hematology and Transfusion Medicine, University Hospital Bonn, 53127 Bonn, Germany.ORCID 0000-0002-3028-1515
Hannah L McRaeInstitute of Experimental Hematology and Transfusion Medicine, University Hospital Bonn, 53127 Bonn, Germany.ORCID 0000-0001-5216-6270
Jens MüllerInstitute of Experimental Hematology and Transfusion Medicine, University Hospital Bonn, 53127 Bonn, Germany.ORCID 0000-0001-7713-9631
Christian P StrassburgDepartment of Internal Medicine I, University Hospital Bonn, 53127 Bonn, Germany.
Johannes OldenburgInstitute of Experimental Hematology and Transfusion Medicine, University Hospital Bonn, 53127 Bonn, Germany.ORCID 0000-0002-1585-4100
Bernd PötzschInstitute of Experimental Hematology and Transfusion Medicine, University Hospital Bonn, 53127 Bonn, Germany.
Christian JansenDepartment of Internal Medicine I, University Hospital Bonn, 53127 Bonn, Germany.ORCID 0000-0003-4475-9644
Heiko RühlInstitute of Experimental Hematology and Transfusion Medicine, University Hospital Bonn, 53127 Bonn, Germany.ORCID 0000-0003-0672-2453

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Splanchnic vein thrombosis (SVT), which is particularly prevalent in myeloproliferative neoplasms (MPNs), has a multifactorial pathomechanism involving the anticoagulant protein C (PC) pathway. To better characterize the hypercoagulable state in SVT we assessed its key enzymes thrombin and activated PC (APC). The study population included 73 patients with SVT, thereof 36 MPN+, confirmed by bone marrow biopsy, 37 MPN-, and 30 healthy controls. Direct measurement of the active enzyme forms of thrombin and APC in the circulation was achieved by using oligonucleotide-based enzyme capture assays (OECA). Additionally, activation markers of coagulation and fibrinolysis were measured. Plasma levels of free thrombin and APC were higher in the MPN+ than in the MPN- cohort, with 0.49 vs. <0.46 pmol/L (

Indexed as

Protein CThrombinThrombophiliaVenous ThrombosisAdultAgedBiomarkersBlood CoagulationCase-Control StudiesFemaleHemostasisHumansMaleMiddle AgedMyeloproliferative DisordersSplanchnic CirculationBiomarkersProtein CThrombinactivated protein Chypercoagulabilitymyeloproliferative neoplasmssplanchnic vein thrombosisthrombin

Identifiers

PMID39796151
PMCPMC11719462

What OpenQuestion holds

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Registered trials

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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.