Evidence map›Paper›PMID 36479816›Full record

ArticleJournal of cellular and molecular medicine2023

Pro-haemostatic effect of DDAVP is partially derived through non-classical (CD14

Laleh Salarilak, Zahra Pirdel, Hossein Dinmohammadi, Hassan Rokni-Zadeh, Renaud Lavend'homme, Mehran Karimi, Marc Jacquemin, Tina Shahani

Open access · goldAbstract read
In one paragraph

Article in Journal of cellular and molecular medicine, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.2field-weighted citation impact, top 44% 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

1 citing paper in PubMed, 1 citations in OpenAlex.

  1. 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

8 authors at 4 institutions in 2 countries.

Laleh SalarilakDepartment of Genetics and Molecular Medicine, School of Medicine, Zanjan University of Medical Sciences (ZUMS), Zanjan, Iran.
Zahra PirdelDeputy of Research and Technology, Ardabil University of Medical Sciences, Ardabil, Iran.
Hossein DinmohammadiDepartment of Genetics and Molecular Medicine, School of Medicine, Zanjan University of Medical Sciences (ZUMS), Zanjan, Iran.
Hassan Rokni-ZadehZanjan Pharmaceutical Biotechnology Research Center, Zanjan University of Medical Sciences (ZUMS), Zanjan, Iran.
Renaud Lavend'hommeDepartment of Cardiovascular Sciences, Center for Molecular and Vascular Biology, KU Leuven, Leuven, Belgium.
Mehran KarimiHematology Research Center, Shiraz University of Medical Sciences, Shiraz, Iran.
Marc JacqueminDepartment of Cardiovascular Sciences, Center for Molecular and Vascular Biology, KU Leuven, Leuven, Belgium.
Tina ShahaniDepartment of Genetics and Molecular Medicine, School of Medicine, Zanjan University of Medical Sciences (ZUMS), Zanjan, Iran.ORCID 0000-0001-5551-9377
Zanjan University of Medical Sciences · IRVIB-KU Leuven Center for Cancer Biology · BEArdabil University of Medical Sciences · IRShiraz University of Medical Sciences · IR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The splenic endothelial Weibel-palade bodies are one of the most important candidate organelles to release von Willebrand factor upon stimulation with desmopressin. However, the presence of functional desmopressin-specific receptor has not yet been demonstrated on endothelial cells. Experimental evidences are in favour of an indirect pro-haemostatic effect of desmopressin, but the exact mediator and its cellular origin are largely elusive. Here, we report partially hampered desmopressin response in a splenectomised severe haemophilia A/Beta Thalassemia patient without any genetic variant relevant to his incomplete desmopressin response. To further investigate the role of the spleen in this phenomenon, the release of VWF from desmopressin-treated human splenic endothelial cells was assessed in vitro. As a result, desmopressin induced the release of VWF from endothelial cells when the cells were co-cultured with non-classical (CD14

Indexed as

Hemophilia AHemostaticsDeamino Arginine VasopressinEndothelial CellsHumansMonocytesSpleenvon Willebrand FactorDeamino Arginine VasopressinHemostaticsvon Willebrand Factorcoagulation factor VIIIendothelial cellmonocytespleenvon-Willebrand factorwhole-exome sequencing

Identifiers

PMID36479816
PMCPMC9806299
OpenAlexW4310938885

What OpenQuestion holds

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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.