660 results match your criteria: "National medical research center of cardiology[Affiliation]"

Aim: to assess the relation of focal and diffuse left ventricular (LV) fibrosis to left bundle branch block (LBBB).

Materials And Methods: 60 patients with dilated cardiomyopathy and LBBB (DCM-LBBB), 50 DCM-nonLBBB patients, 15 patients with LBBB and structurally normal heart (idiopathic LBBB) and 10 healthy volunteers (HV) underwent cardiovascular magnetic resonance (CMR) with late gadolinium enhancement (LGE). LGE LV images were post-proceed for core scar (CS) and gray zone (GZ) calculation.

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Hypertrophic cardiomyopathy (HCM) is a genetic cardiac disorder associated with an increased risk of arrhythmias, heart failure, and sudden cardiac death. Current imaging and clinical markers are not fully sufficient in accurate diagnosis and patient risk stratification. Although known cardiac biomarkers in blood are used, they lack specificity for HCM and primarily stratify for death due to heart failure in overt cases.

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Article Synopsis
  • * Affected individuals typically experience more severe heart failure symptoms and poorer outcomes, influencing treatment choices based on how severe the dysfunction is.
  • * Echocardiography is a key tool for evaluating left atrial function, and analyzing strain parameters can help identify early issues and guide prognosis and treatment strategies in HFpEF.
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Aim    To analyze the results of myocardial revascularization in the Russian Federation (RF) for ACS in 2023 compared to previous years.Material and methods    The analysis included the number of cases of ST-segment elevation myocardial infarction (STEMI), non-ST-segment elevation acute coronary syndrome (NSTE-ACS), myocardial revascularization in the above-listed ACS forms, the number of fatal outcomes depending on the ACS form and the revascularization method used. The data for this analysis were obtained from the 2023 Ministry of Health of Russia monitoring in the section of revascularization in ACS and were compared with the data for the past 8 years.

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  • The study aimed to identify why patients with chronic heart failure (CHF) in Russia have a poor prognosis, using data from various population samples and medical records over several years.
  • It established the prevalence of CHF in the Russian population, finding that 8.2% of individuals meet soft criteria for CHF, while 3.1% met strict criteria, with significant influences from conditions like hypertension and ischemic heart disease.
  • The prognosis for these patients is grim, with over half dying within four years after acute decompensated heart failure (ADHF), and most patients with severe CHF not surviving beyond ten years, primarily due to inadequate medication use and poor patient follow-up.
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  • The CHANCE study investigated the effects of a monitoring and education program for patients with chronic heart failure, comparing an intervention group (IG) receiving structured support to a control group (CG) receiving standard care.
  • Results showed that the IG had significantly lower mortality rates (8.3%) compared to the CG (13.0%), and a relative risk of 0.68 for death, indicating the program's effectiveness in saving lives.
  • Additionally, the IG exhibited better improvements in clinical condition, functional capabilities (as seen in the 6-minute walk test), and overall quality of life, with significant reductions in anxiety and depressive symptoms over 12 months.
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Pericarditis as an inflammatory heart disease is rarely discussed in the cardiology community. The latest European guidelines on pericarditis were published in 2015, and Russian clinical guidelines are dated 2022. However, in recent years, a number of publications have appeared that have forced the scientific community to take a fresh look at this problem.

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Cognitive impairment is a very common comorbidity in patients with heart failure (HF). Patients with HF show signs of memory decline, difficulty concentrating, and attention deficits. Cognitive dysfunction in HF is associated with a poor prognosis.

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Dilated cardiomyopathy (DCM) is a leading cause of heart failure, sudden cardiac death, and heart transplantation in young patients. The causes of DCM are varied and include genetic factors and metabolic, infectious, toxic and others factors. Today it is known that germline mutations in more than 98 genes can be associated with the occurrence of DCM.

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Aim: To analyze the experience of Chazov National Medical Research Center of Cardiology in patient selection for left ventricular assist device (LVAD) implantation.

Materials And Methods: 901 patients, whose documents were sent to Chazov National Medical Research Center of Cardiology from regional medical and prophylactic institutions, were screened as selection for LVAD implantation. Firstly, all patients underwent transthoracic echocardiography performed according to the extended protocol with a comprehensive assessment of the left and right ventricle size and function.

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  • The study aimed to explore how metabolic disorders and obesity affect hemodynamic parameters in patients with chronic thromboembolic pulmonary hypertension (CTEPH) using data from the POLET registry.
  • The research analyzed various medical factors from 84 patients, including their metabolic profiles, functional capacity, and heart health metrics like right heart catheterization and echocardiography.
  • Findings revealed significant correlations between right atrial area and lipid levels, indicating that older patients with severe functional classes (mostly III and IV) may experience a greater impact from metabolic issues, which is crucial for assessing patient risk of death.
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Background: Arterial hypertension (AH) remains the leading risk factor associated with cardiovascular diseases (CVDs), cerebrovascular disease and chronic kidney disease. About 70% of patients with AH who are on monotherapy cannot achieve blood pressure (BP) targets, and therefore all quidelines for the management of AH have recently recommended prescribing combination therapy (PCT). In real clinical practice (RCP), there remains significant uncertainty in the effectiveness and rationality of therapy, despite the wide availability of antihypertensive drugs (AHD) and the presence of recommendations for a stepwise approach to prescribing combinations of specific groups of AHD in different clinical situations.

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Background: Thoracic aortic aneurysm is a latent disease with a high risk of death. Today, as data are accumulating, an estimation of the differences in thoracic aneurysm in men and women of different age groups is required. The present study evaluated the type of atherosclerotic aortic lesions in males and females at different ages regarding the presence or absence of aortic dissection.

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Increased platelet activity is a risk factor of thrombotic events in cardiovascular patients. We studied the relationship between platelet function, platelet size, and the content of reticulated platelets (RP) in patients with coronary heart disease (CHD, n = 55) and acute coronary syndrome (ACS, n = 95) receiving acetylsalicylic acid + clopidogrel or ticagrelor, respectively. The control group consisted of patients with risk factors for CHD, but with no CHD/ACS and free of antiplatelet drugs (n = 66).

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Unlabelled: In recent years, the prevalence of thoracic aortic aneurysm has increased, and in most cases this pathological condition is diagnosed accidentally. The aim of the current study was to determine the relationship of clinical, laboratory and morphological data with the presence of aorta wall dissection in patients with thoracic aortic aneurysm to reveal factors associated with aorta dissection.

Materials And Methods: The following data of 109 patients mean aged of 53 years with thoracic aortic aneurysm (43 patients with aortic dissection) were analyzed: presence/absence of arterial hypertension, indicators of general blood analysis and blood biochemistry, immunomorphological characteristics of the expression of Von Willebrand factor.

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  • Barth syndrome is a rare genetic disorder linked to abnormal cardiolipin metabolism, leading to high mortality rates, especially from heart issues and infections within 5 years of being diagnosed.
  • The article presents a clinical case of an adult patient, highlighting the disease's progression from hypertrophic cardiomyopathy to hypokinetic cardiomyopathy as the patient aged.
  • It emphasizes the challenges in finding effective treatment options for Barth syndrome due to a lack of definitive guidelines and targeted therapies in clinical practice.
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  • * It used a modeling method to compare the clinical benefits and economic costs of dapagliflozin against standard therapies, factoring in local healthcare costs.
  • * Results showed that dapagliflozin improved life expectancy and reduced hospital visits, with the cost per additional year of life being lower than the willingness-to-pay threshold, making it a cost-effective option regardless of the initial therapy used.
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  • * The study used a modified cell line containing the m.15059G>A mutation to assess the impacts of eliminating this mutation on mitochondrial function.
  • * Results showed that removing the m.15059G>A mutation enhanced mitochondrial membrane potential and efficiency, reduced harmful byproducts, and did not alter the antioxidant system, indicating the mutation's negative role in mitochondrial health.
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  • The study aimed to identify predictors of adverse cardiovascular events following edge-to-edge transcatheter mitral valve repair (TMVR) in patients with severe mitral regurgitation (MR), focusing on heart structure and function changes over time.
  • It involved 73 high surgical risk patients (average age 71) who underwent TMVR, measuring various heart metrics before, shortly after, and one year post-procedure, including myocardial function and NT-proBNP levels.
  • Results showed a significant reduction in MR in both primary and secondary categories within 12 months, alongside changes in heart chamber size and improvements in certain functional metrics, despite initial impairments in left ventricular function right after surgery.
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Unlabelled: Аims: This research aimed to study the features of gene regulation of the inflammatory response in cells carrying mitochondrial mutations associated with atherosclerosis.

Background: Inflammation plays an important, if not decisive, role in the occurrence of atherosclerotic lesions and then accompanies it throughout its further development. Thus, atherogenesis is a chronic inflammatory process.

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The burden of heart failure (HF) has been increasing worldwide in recent decades. Early diagnosis of HF based on the outpatient measurement of natriuretic peptide (NP) concentration will allow timely initiation of the treatment and reducing the incidence of adverse outcomes in HF. Unfortunately, the frequency of NP testing remains low worldwide.

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Aim: To study the relaxation structure of the left ventricle (LV) in patients who underwent ventriculography.

Material And Methods: LV ventriculography was performed in 37 patients. Before catheterization, echocardiography was performed in each patient.

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This review summarises the data from long-term experimental studies and literature data on the role of oxidatively modified low-density lipoproteins (LDL) in atherogenesis and diabetogenesis. It was shown that not "oxidized" (lipoperoxide-containing) LDL, but dicarbonyl-modified LDL are atherogenic (actively captured by cultured macrophages with the help of scavenger receptors), and also cause expression of lectin like oxidized low density lipoprotein receptor 1 () and nicotinamide adenine dinucleotide phosphate (NADPH) oxidase 1 () genes in endotheliocytes, which stimulate apoptosis and endothelial dysfunction. The obtained data allowed us to justify new approaches to pharmacotherapy of atherosclerosis and diabetes mellitus.

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  • * Using PCR and pyrosequencing, researchers identified various mtDNA mutations, noting four proatherogenic (harmful) and three antiatherogenic (protective) mutations.
  • * The study also revealed a geographic pattern in the distribution of certain mutations, highlighting a west-east gradient in specific mtDNA mutations associated with atherosclerosis.
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Background: Cells of different human organs and tissues contain different numbers of mitochondria. In these organelles, there are different copies of the mitochondrial genome, which is characteristic of a certain organ or tissue.

Objective: The aim of the investigation was to analyze the results of scientific works dedicated to the analysis of heteroplasmy levels of mitochondrial genome mutations in a number of organs and tissues.

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