Publications by authors named "Matteo Beltrami"

Background: Cardiovascular diseases (CVDs) and chronic kidney disease (CKD) are common causes of morbidity and mortality. However, the impact of changes in lifestyle and rehabilitation programs on the progression of cardiovascular, renal, and metabolic (CRM) conditions, remains unclear.

Methods: In a retrospective manner, we analyzed charts of 200 patients admitted for cardiorespiratory rehabilitation at our facility in 2023.

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  • The HF syndrome involves an imbalance in the autonomic nervous system, leading to an increase in sympathetic activity and various cardiac changes that result in chronotropic incompetence (CI), or the inability to raise heart rate with activity.
  • CI is linked to decreased exercise capacity and poorer health outcomes, and the definition of CI can vary, complicating its assessment.
  • While β-blockers can lower peak heart rate, they improve prognosis in heart failure, and strategies like rate-adapting pacing are being explored to address the reduced heart rate response during exercise.
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Lung ultrasound (LUS) is a simple, fast and non-invasive tool for pulmonary congestion assessment with higher accuracy for the detection of acute heart failure (HF) compared to clinical examination and chest radiography. The integrated assessment with other ultrasound and echocardiographic parameters can lead to a better systemic and pulmonary congestion characterization. Additionally, the combination of echocardiographic and pulmonary features can identify patients at higher risk for adverse outcomes, potentially facilitating both acute and chronic HF management and prognostic stratification.

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  • HFpEF is a complex condition influenced by factors like age, genetics, and various health issues, including kidney disease, which significantly affects its progression and management.
  • The relationship between heart failure (HF) and chronic kidney disease (CKD) is intricate, as both share similar biological pathways and pose challenges for effective treatment due to patients often not being well-represented in clinical trials.
  • Newer medications, particularly SGLT2 inhibitors, show promise for treating patients with both HFpEF and CKD, highlighting the importance of understanding their cardiorenal interactions for improved management strategies.
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  • PAH is a rare but serious condition marked by high pressure in the pulmonary arteries, which can lead to right heart problems and life-threatening issues.
  • The disease involves a variety of complex mechanisms like vasoconstriction and inflammation, influenced by various molecular pathways including nitric oxide and prostacyclin.
  • Despite the importance of early diagnosis, PAH currently lacks effective biomarkers, and research aims to identify new biomarkers to improve diagnosis, prognosis, and monitoring of treatment.
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Hypertrophic cardiomyopathy (HCM) is a leading cause of lethal arrhythmias in the young. Although the arrhythmic substrate has been hypothesised to be amenable to late Na block with ranolazine, the specific mechanisms are not fully understood. Therefore, this study aimed to investigate the substrate mechanisms of safety and antiarrhythmic efficacy of ranolazine in HCM.

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Heart failure (HF) represents a significant global health challenge, characterized by high morbidity and mortality rates, and imposes considerable burdens on healthcare systems and patient quality of life. Traditional management strategies, primarily relying on clinical assessments and standard biomarkers like natriuretic peptides, face limitations due to the heterogeneity of HF. This review aims to delve into the evolving landscape of non-natriuretic biomarkers and the transformative potential of omics technologies, underscoring their roles in advancing HF treatment towards precision medicine.

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  • Acute myocarditis presents a range of clinical forms, from mild to severe, all characterized by inflammation of the heart muscle, which can lead to complications like unstable blood flow and irregular heart rhythms.
  • * Chronic inflammatory cardiomyopathy is a long-lasting condition that results in heart failure symptoms and an increased risk of arrhythmias, showing a connection between acute and chronic heart issues.
  • * Early diagnosis is crucial, with tools like cardiac MRI and endomyocardial biopsy being important for identifying the condition, along with genetic counseling if genetic links are suspected for better patient outcomes.*
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Background: Pseudonormal T waves may be detected on stress electrocardiograms (ECGs) in hypertrophic cardiomyopathy (HCM). Either myocardial ischaemia or purely exercise-induced changes have been hypothesised to contribute to this phenomenon, but the precise electrophysiological mechanisms remain unknown.

Methods: Computational models of human HCM ventricles (n = 20) with apical and asymmetric septal hypertrophy phenotypes with variable severities of repolarisation impairment were used to investigate the effects of acute myocardial ischaemia on ECGs with T wave inversions at baseline.

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Heart failure (HF) is a progressive condition with a clinical picture resulting from reduced cardiac output (CO) and/or elevated left ventricular (LV) filling pressures (LVFP). The original Diamond-Forrester classification, based on haemodynamic data reflecting CO and pulmonary congestion, was introduced to grade severity, manage, and risk stratify advanced HF patients, providing evidence that survival progressively worsened for those classified as warm/dry, cold/dry, warm/wet, and cold/wet. Invasive haemodynamic evaluation in critically ill patients has been replaced by non-invasive haemodynamic phenotype profiling using echocardiography.

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Aims: The role of pre-participation screening (PPS) modalities in preventing sudden cardiac death (SCD) in athletes is debated due to a high false-positive rate. Focused cardiac ultrasound (FoCUS) has shown higher sensitivity and specificity, but its cost-effectiveness remains uncertain. This study aimed to determine the diagnostic performance and cost-effectiveness of FoCUS use in PPS.

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Cardiomyopathies are a heterogeneous group of myocardial diseases representing the first cause of heart transplantation in children. Diagnosing and classifying the different phenotypes can be challenging, particularly in this age group, where cardiomyopathies are often overlooked until the onset of severe symptoms. Cardiovascular imaging is crucial in the diagnostic pathway, from screening to classification and follow-up assessment.

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  • The study focuses on two sarcomere genes linked to hypertrophic cardiomyopathy (HCM), specifically MYBPC3 and MYH7, and examines their impact on heart function over time.
  • Researchers reviewed echocardiograms of 402 HCM patients and found MYBPC3 mutation carriers experienced a higher rate of severe left ventricular dysfunction compared to MYH7 mutation carriers, despite both groups showing a small decline in heart function over time.
  • The findings suggest that while both gene mutations lead to HCM, MYBPC3 mutations are associated with a greater risk of long-term systolic dysfunction, underscoring the need for tailored monitoring and management strategies in affected patients.
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Background: Cardiac resynchronization therapy (CRT) is an established treatment in selected patients suffering from heart failure with reduced ejection fraction (HFrEF). It has been proposed that myocardial fibrosis and inflammation could influence CRT "response" and outcome. Our study investigated the long-term prognostic significance of cardiac biomarkers in HFrEF patients with an indication for CRT.

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Introduction: Patients with hypertrophic cardiomyopathy (HCM) are at increased risk of stroke, but the incidence and factors associated with cardioembolic events in HCM patients without atrial fibrillation (AF) remain unresolved. We determined the incidence of stroke in patients in sinus rhythm (SR) monitored with a cardiac implantable electronic device (CIED).

Methods: All consecutive patients diagnosed with HCM and referred to CIED implantation with >16 years at diagnosis and ≥ 1 year follow-up post CIED implantation were retrospectively reviewed.

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Epicardial adipose tissue (EAT) is an endocrine and paracrine organ constituted by a layer of adipose tissue directly located between the myocardium and visceral pericardium. Under physiological conditions, EAT exerts protective effects of brown-like fat characteristics, metabolizing excess fatty acids, and secreting anti-inflammatory and anti-fibrotic cytokines. In certain pathological conditions, EAT acquires a proatherogenic transcriptional profile resulting in increased synthesis of biologically active adipocytokines with proinflammatory properties, promoting oxidative stress, and finally causing endothelial damage.

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  • * COVID-19 can worsen heart function due to direct damage and complications related to the virus, which may lead to arrhythmias and fluid retention in patients with HF.
  • * Effective management strategies tailored for HF patients infected with COVID-19 are crucial to minimize cardiovascular complications and ensure better health outcomes.
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  • - Hypertrophic cardiomyopathy (HCM) exhibits diverse progression patterns toward serious issues like heart failure and sudden cardiac death, necessitating a tailored approach rather than a one-size-fits-all method seen in other heart conditions.
  • - Utilizing multiple imaging techniques combined with artificial intelligence can enhance the diagnosis and management of HCM, but requires deep understanding of clinical progression and patient-specific features.
  • - The review emphasizes the significance of recognizing specific "red alerts" to better connect the genetic and phenotypic characteristics of patients with sarcomeric HCM, while also addressing ongoing challenges in imaging standardization and timing.
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Heart failure with preserved ejection fraction (HFpEF) remains a poorly characterized syndrome with many unknown aspects related to different patient profiles, various associated risk factors and a wide range of aetiologies. It comprises several pathophysiological pathways, such as endothelial dysfunction, myocardial fibrosis, extracellular matrix deposition and intense inflammatory system activation. Until now, HFpEF has only been described with regard to clinical features and its most commonly associated risk factors, disregarding all biological mechanisms responsible for cardiovascular deteriorations.

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  • Hypertrophic cardiomyopathy (HCM) is a common inherited heart disease that increases the risk of heart failure and sudden cardiac death, yet effective risk assessment remains challenging.
  • This study analyzed various factors, including demographic, clinical, biochemical, and imaging findings, from 112 studies involving over 58,000 HCM patients to evaluate their prognostic significance.
  • Results indicated that advanced imaging techniques, particularly late gadolinium enhancement (LGE), provided the best risk predictions, suggesting that multiparametric models incorporating these advanced markers could improve patient risk stratification.
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  • Pulmonary arterial hypertension (PAH) is common in patients with hypertrophic cardiomyopathy (HCM) and negatively affects their health outlook, especially during exercise.
  • A study involving 182 HCM patients used cardiopulmonary exercise tests (CPET) and echocardiography to identify exercise-induced PAH (EiPAH), finding that 20% of patients experienced significant increases in pulmonary pressure during exertion.
  • The presence of EiPAH was linked to poorer exercise performance and increased risk of HCM-related complications, suggesting that diagnosing it early can lead to better monitoring and treatment options for patients.
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The evaluation of left ventricular (dys)function is at the core of clinical cardiology practice in patients with hypertrophic cardiomyopathy. Hypertrophic cardiomyopathy proceeds along paradigms that are profoundly different and follows disease-specific patterns of progression towards heart failure. By automatically applying a standard approach, much information is lost or misplaced, and severe degrees of dysfunction may be erroneously interpreted as mild by such an assumption.

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In recent years, new interest is growing in the left atrium (LA). LA functional analysis and measurement have an essential role in cardiac function evaluation. Left atrial size and function are key elements during the noninvasive analysis of diastolic function in several heart diseases.

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Aims: Ventricular cardiomyocytes from hypertrophic cardiomyopathy (HCM) patient hearts show prolonged action potential duration (APD), impaired intracellular Ca homeostasis and abnormal electrical response to beta -adrenergic stimulation. We sought to determine whether this behaviour is associated with abnormal changes of repolarization during exercise and worsening of diastolic function, ultimately explaining the intolerance to exercise experienced by some patients without obstruction.

Methods And Results: Non-obstructive HCM patients (178) and control subjects (81) underwent standard exercise testing, including exercise echocardiography.

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Patients with heart failure (HF) and associated chronic kidney disease (CKD) are a population less represented in clinical trials; additionally, subjects with more severe estimated glomerular filtration rate reduction are often excluded from large studies. In this setting, most of the data come from post hoc analyses and retrospective studies. Accordingly, in patients with advanced CKD, there are no specific studies evaluating the long-term effects of the traditional drugs commonly administered in HF.

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