Clinical Research Directory

Inclusion Criteria: * Patients ≥ 18 years old * Signed patient informed consent form (ICF) * Diagnosis of chronic (documented HF hospitalization in the last year) or acute decompensated HF shown by signs and symptoms of HF and LVEF \>50% and, according to guidelines and the universal definition of HF, elevated levels of natriuretic peptides (NT-proBNP ≥300 pg/ml in sinus rhythm or NTproBNP ≥600 pg/ml in atrial fibrillation), at the time of enrolment (10) * Echocardiographic evidence of increased estimated LV filling pressures according to current guidelines Exclusion Criteria: * Planned participation or participation in a clinical trial; * Life expectancy \< 1 year because of non-cardiac causes; * History of recent (6 months) infective, or inflammatory, autoimmune or neoplastic diseases. * Stage \>4 CKD (estimated glomerular filtration rate \[eGFR\] \< 15 ml/min/1.73m2), * Myocardial infarction (increase in cardiac enzymes in combination with symptoms of ischemia or newly developed ischemic ECG changes), coronary artery bypass graft surgery or other major cardiovascular surgery, stroke or TIA in past 3 months; * Chronic pulmonary disease requiring home oxygen, oral steroid therapy or hospitalization for exacerbation within 12 months; * Congenital heart disease. * Primary pulmonary hypertension * Moderate-to-severe degenerative (primary) valve disease * Cardiomyopathy based on muscular dystrophies, cardiomyopathy with reversible causes (e.g. stress cardiomyopathy), or known pericardial constriction; * Implantation of cardioverter defibrillator (ICD) within 3 months * Implanted cardiac resynchronization therapy (CRT) and/or stable RV pacing.