Publications by authors named "L G Kovalenko"

Article Synopsis
  • The study develops a machine learning model to predict major adverse cardiac events (MACEs) in high-risk myocardial infarction (MI) patients, incorporating clinical, imaging, laboratory, and genetic data.
  • It analyzes data from 218 MI patients over 9 years, focusing on the influence of the VEGFR-2 gene variant as part of the overall risk assessment.
  • The CatBoost algorithm performed best, with statin dosage and genetic factors identified as key predictors of adverse events, highlighting the potential for personalized treatment approaches based on genetic information.
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The bitter drug, warfarin, has a narrow therapeutic index (NTI) and is used in paediatrics and geriatrics. The aim of this feasibility study was to formulate the taste-masked warfarin-containing pellets to be applicable for dose personalisation and to improve patient compliance, as well as to investigate the effect of the core type (PharSQ Spheres M, CELPHERE™ CP-507, and NaCl) on the warfarin release from the Kollicoat Smartseal taste-masking-coated pellets. The cores were successfully drug-loaded and coated in a fluid-bed coater with a Wurster insert.

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Osteogenesis imperfecta (OI) is a group of inherited disorders of connective tissue that cause significant deformities and fragility in bones. Most cases of OI are associated with pathogenic variants in collagen type I genes and are characterized by pronounced polymorphisms in clinical manifestations and the absence of clear phenotype-genotype correlation. The objective of this study was to conduct a comprehensive molecular-genetic and clinical analysis to verify the diagnosis of OI in six Russian patients with genetic variants in the and genes.

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Natural and synthetic phytohormones are widely used in agriculture. The synthetic cytokinin ethylenediurea (EDU) induces protection in plants against ozone phytotoxicity. In our study, new hybrid derivatives of EDU were synthesized and tested for phytoactivity.

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Background: Potocki-Lupski syndrome (PTLS, OMIM # 610883) is a rare genetic developmental disorder resulting from a partial heterozygous microduplication at chromosome 17p11.2. The condition is characterized by a wide variability of clinical expression, which can make its clinical and molecular diagnosis challenging.

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