Evidence map›Paper›PMID 36362759›Full record

ArticleJournal of clinical medicine2022

DNA Polymorphisms in Pregnant Women with Sticky Platelet Syndrome.

Lucia Stančiaková, Jana Žolková, Ľubica Vadelová, Andrea Hornáková, Zuzana Kolková, Martin Vážan, Miroslava Dobrotová, Pavol Hollý, Zuzana Jedináková, Marián Grendár and 8 more

Open access · goldAbstract read
In one paragraph

Article in Journal of clinical medicine, 2022. 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
–field-weighted citation impact, top 74% 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, 0 citations in OpenAlex.

  1. SelectedClinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis
    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

18 authors at 3 institutions in 1 country.

Lucia StančiakováNational Centre of Haemostasis and Thrombosis, Department of Haematology and Transfusion Medicine, Jessenius Faculty of Medicine in Martin, Comenius University in Bratislava, Martin University Hospital, 036 59 Martin, Slovakia.ORCID 0000-0001-8086-1422
Jana ŽolkováNational Centre of Haemostasis and Thrombosis, Department of Haematology and Transfusion Medicine, Jessenius Faculty of Medicine in Martin, Comenius University in Bratislava, Martin University Hospital, 036 59 Martin, Slovakia.
Ľubica VadelováNational Centre of Haemostasis and Thrombosis, Department of Haematology and Transfusion Medicine, Jessenius Faculty of Medicine in Martin, Comenius University in Bratislava, Martin University Hospital, 036 59 Martin, Slovakia.
Andrea HornákováBiomedical Centre Martin, Jessenius Faculty of Medicine in Martin, Comenius University in Bratislava, 036 01 Martin, Slovakia.
Zuzana KolkováBiomedical Centre Martin, Jessenius Faculty of Medicine in Martin, Comenius University in Bratislava, 036 01 Martin, Slovakia.
Martin VážanDepartment of Medical Genetics, Martin University Hospital, 036 59 Martin, Slovakia.
Miroslava DobrotováNational Centre of Haemostasis and Thrombosis, Department of Haematology and Transfusion Medicine, Jessenius Faculty of Medicine in Martin, Comenius University in Bratislava, Martin University Hospital, 036 59 Martin, Slovakia.
Pavol HollýNational Centre of Haemostasis and Thrombosis, Department of Haematology and Transfusion Medicine, Jessenius Faculty of Medicine in Martin, Comenius University in Bratislava, Martin University Hospital, 036 59 Martin, Slovakia.
Zuzana JedinákováNational Centre of Haemostasis and Thrombosis, Department of Haematology and Transfusion Medicine, Jessenius Faculty of Medicine in Martin, Comenius University in Bratislava, Martin University Hospital, 036 59 Martin, Slovakia.
Marián GrendárLaboratory of Bioinformatics and Biostatistics, Biomedical Centre Martin, Jessenius Faculty of Medicine in Martin, Comenius University in Bratislava, 036 01 Martin, Slovakia.
Tomáš BolekDepartment of Internal Medicine I., Jessenius Faculty of Medicine in Martin, Comenius University in Bratislava, Martin University Hospital, 036 59 Martin, Slovakia.
Matej SamošDepartment of Internal Medicine I., Jessenius Faculty of Medicine in Martin, Comenius University in Bratislava, Martin University Hospital, 036 59 Martin, Slovakia.ORCID 0000-0002-5561-2560
Kamil BiringerDepartment of Gynaecology and Obstetrics, Jessenius Faculty of Medicine in Martin, Comenius University in Bratislava, Martin University Hospital, 036 59 Martin, Slovakia.ORCID 0000-0002-3471-0508
Ján DankoDepartment of Gynaecology and Obstetrics, Jessenius Faculty of Medicine in Martin, Comenius University in Bratislava, Martin University Hospital, 036 59 Martin, Slovakia.
Tatiana BurjanivováBiomedical Centre Martin, Jessenius Faculty of Medicine in Martin, Comenius University in Bratislava, 036 01 Martin, Slovakia.
Zora LasabováBiomedical Centre Martin, Jessenius Faculty of Medicine in Martin, Comenius University in Bratislava, 036 01 Martin, Slovakia.
Peter KubiszNational Centre of Haemostasis and Thrombosis, Department of Haematology and Transfusion Medicine, Jessenius Faculty of Medicine in Martin, Comenius University in Bratislava, Martin University Hospital, 036 59 Martin, Slovakia.
Ján StaškoNational Centre of Haemostasis and Thrombosis, Department of Haematology and Transfusion Medicine, Jessenius Faculty of Medicine in Martin, Comenius University in Bratislava, Martin University Hospital, 036 59 Martin, Slovakia.ORCID 0000-0003-3305-0269
Martin University Hospital · SKComenius University Bratislava · SKSlovak Academy of Sciences · SK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Sticky platelet syndrome (SPS) is a thrombophilia caused by the increased aggregability of platelets in response to the addition of low concentrations of epinephrine (EPI) and/or adenosine diphosphate (ADP). Some of the single nucleotide polymorphisms (SNP), alleles and haplotypes of platelet glycoprotein receptors were proved to have a role in the etiology of thrombotic episodes When comparing SPS and the control group, in VEGFA rs3025039, the p value for both CC vs. TT and CT vs. TT analyses was <0.001. Interestingly, no minor TT genotype was present in the SPS group, suggesting the thrombotic pathogenesis of recurrent spontaneous abortions (RSA) in these patients. Moreover, we found a significant difference in the presence of AT containing a risky A allele and TT genotype of ALPP rs13026692 (p = 0.034) in SPS patients when compared with the controls. Additionally, we detected a decreased frequency of the GG (CC) genotype of FOXP3 rs3761548 in patients with SPS and RSA when compared with the control group (p value for the CC (GG) vs. AA (TT) 0.021). This might indicate an evolutionary protective mechanism of the A (T) allele in the SPS group against thrombotic complications in pregnancy. These results can be used for antithrombotic management in such pregnant patients.

Indexed as

antithrombotic treatmentDNA analysispolymorphismssticky platelet syndrome

Identifiers

PMID36362759
PMCPMC9657965
OpenAlexW4308333465

What OpenQuestion 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 OpenQuestion graph.