Publications by authors named "Ieva Ciapiene"

Article Synopsis
  • Coronary microvascular dysfunction (CMD) often occurs after ST-elevation myocardial infarction (STEMI) and can negatively impact patient outcomes; TMAO, a gut microbiota metabolite, may help diagnose CMD in these patients.
  • In a study involving 210 STEMI patients, TMAO levels were measured at various points, with a key finding being that TMAO at 3 months was a more reliable indicator for diagnosing CMD compared to baseline levels.
  • The research concluded that high TMAO levels (≥3.91) were linked to a greater risk of major adverse cardiovascular and cerebrovascular events (MACCE), highlighting TMAO's potential as a biomarker that could enhance
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Article Synopsis
  • * In a study with 92 patients experiencing acute coronary syndromes, about 29% were identified as poor metabolizers of the CYP2C19 gene, which resulted in a significantly lower response to atorvastatin treatment compared to normal metabolizers.
  • * The findings suggest that factors like the CYP2C19 metabolizing phenotype, patient age, and smoking status can increase the risk of inadequate treatment outcomes, highlighting the importance of tailoring atorvastatin therapy based on genetic profiles.
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  • The pilot study investigated how placental mesenchymal stem/stromal cells (MSCs) affect immune cells from patients with hidradenitis suppurativa (HS) by examining peripheral blood mononuclear cells (PBMCs) from both healthy individuals and HS patients.
  • PBMCs from HS patients displayed higher levels of the pro-inflammatory cytokines IL-6 and IFN-γ compared to those from healthy subjects, indicating increased inflammation.
  • The study found that co-culture with activated MSCs significantly reduced PBMC proliferation and inflammatory cytokine production, suggesting MSCs may have therapeutic potential for HS, although further research with a larger sample size is needed for confirmation.
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Background: Ischemic heart disease (IHD) is the most prevalent type of cardiovascular disease. The main cause of IHD is atherosclerosis, which is a multifactorial inflammatory disease of blood vessels. Studies show that bacteria might have a significant impact on the pathogenesis of atherosclerosis and plaque rupture.

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Interindividual variability in drug response is a major problem in the prescription of pharmacological treatments. The therapeutic effect of drugs can be influenced by human genes. Pharmacogenomic guidelines for individualization of treatment have been validated and used for conventional dosage forms.

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Purpose: The aim of this study was to determine the effect of genetic polymorphism and renal function on the occurrence of ticagrelor-related dyspnea.

Patients And Methods: A total of 299 patients with acute with type 1, 2, or 3 myocardial infarction (with and without ST-segment elevation), who underwent coronary angiography and PTCA with stent implantation and were treated with antiplatelet drugs (ticagrelor and aspirin), were enrolled in this prospective study. For all enrolled patient's platelet aggregation (induction with high-sensitivity adenosine diphosphate, ADP HS) testing was performed using a MULTIPLATE analyzer.

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This study investigates the therapeutic potential of human placental mesenchymal stem cells (P-MSCs) and their extracellular vesicles (EVs) in a murine model of acute respiratory distress syndrome (ARDS), a condition with growing relevance due to its association with severe COVID-19. We induced ARDS-like lung injury in mice using intranasal LPS instillation and evaluated histological changes, neutrophil accumulation via immunohistochemistry, bronchoalveolar lavage fluid cell count, total protein, and cytokine concentration, as well as lung gene expression changes at three time points: 24, 72, and 168 h. We found that both P-MSCs and EV treatments reduced the histological evidence of lung injury, decreased neutrophil infiltration, and improved alveolar barrier integrity.

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Background/objectives: To investigate the associations between ophthalmic parameters, CYP4F2 (rs2108622) and ABCA1 (rs1883025) polymorphisms and coronary artery disease, considering the accessibility, non-invasive origin of retinal examination and its possible resemblance to coronary arteries.

Subjects/methods: Overall 165 participants divided into groups based on the coronary angiography results and clinical status: control group (N = 73), MI group (N = 63), 3VD (three vessel disease) (N = 24). All the participants underwent total ophthalmic examination - optical coherence tomography (OCT) and OCT angiography of the macula region were performed and evaluated.

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Background: Antiplatelet drugs, such as ticagrelor, which target platelet P2Y receptors, are used for prevention of ischemic heart disease. Ticagrelor is also known to have pleiotropic effects of unknown mechanisms. Ticagrelor could influence the expression of molecules involved in resolution of inflammation.

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ESBL-producing and bacterial biofilms-forming are associated with antimicrobial treatment failure. This study aimed to investigate the phenotypic resistance mechanisms of CTX-M against old antibiotics - cell wall synthesis inhibitors temocillin, nitrofurantoin and fosfomycin. Susceptibility to old antibiotics testing was performed using disk diffusion method, biofilm formation was evaluated spectrophotometrically, and PCR was used for the determination of CTX-M type.

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The goals of this study were to develop a new technique that could pave the way for a quicker determination of rs3093135 and rs4244285 variants directly from a patient's blood and to attempt to apply this technique in clinical practice. The study included 144 consecutive patients admitted with ST elevation myocardial infarction. A blood-direct PCR and real-time PCR were used to detect variants of interest.

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