Year: 2022
Type: article
Study design: Observational Study
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.
Source: Journal of Clinical Medicine
DOI: 10.3390/jcm11216532
Language: English
Subfield: Hematology
Field: Medicine
Domain: Health Sciences
Open Access status: gold
Estimated APC paid: $2,513
Awards: G1236497349, G1313335969, G1767333005, Využitie monitorovania zmien hemostázy a detekcie mikroRNA v predikcii tehotenských komplikácií u žien s rizikovou tehotnosťou., Využitie výsledkov analýzy DNA a detekcie mikroRNA v primárnej a sekundárnej profylaxii tromboembolických komplikácií u pacientov so syndrómom lepivých doštičiek, Špecifické laboratórne monitorovanie reaktivity trombocytov u pacientov s akútnym infarktom myokardu liečených novými antagonistami P2Y12 receptora, G7840712915, Molekulárno-genetické aspekty hyperagregability trombocytov u pacientov s venóznym tromboembolizmom, G8340464814
OpenAlex ID: W4308333465
