Heart Failure, Heart Failure With Preserved Ejection Fraction
Conditions
Brief summary
This is a prospective multicenter study to decipher phenotypic variability within patients with heart failure and preserved left ventricular ejection fraction (HFpEF). From a registry of heart failure patients (2500 anticipated) hospitalized in the participating centers in the last 3 years, up to 300 participants (with a final ratio of 3 HFpEF patients, 2 patients with heart failure and reduced ejection fraction (HFrEF) and 1 matched subjects without heart failure will be enrolled for an extensive phenotyping with physical evaluation, biomarkers and omics, cardiac and vascular imaging and telemonitoring of cardiovascular parameters. Cluster analysis with machine learning methods will be performed to define phenogroups unique to the HFpEF patient population.
Detailed description
Heart failure with preserved ejection fraction (HFpEF) is a complex and prevalent syndrome with currently no efficient therapy. This syndrome is likely explained by different pathophysiological inputs leading to common symptoms of heart failure. These pathophysiological abnormalities can primarily involve the heart but also other organs with secondary impact on the myocardium. There is however no clear understanding and diagnostic algorithms of the different HFpEF subpopulations. Novel mathematical methods (such as machine learning) can help identifying clusters within an heterogeneous population such as HFpEF patients. A registry (2500 anticipated) will be constituted with patients hospitalized for congestive heart failure in the participating centers during the last 3 years. From this registry, up to 500 patients will be invited to visit in the hospital for 8-10 hours for physical examination, ECG, performance-based tests, blood draw, cMRI, echocardiography (rest and low-level exercise), Ultrafast echo (for non-invasive measurement of myocardial stiffness), low radiation cardiac CT (for calcium scoring), non-invasive measurement of arterial stiffness. They will be asked to fill out questionnaires about dyspnea, depression and about general health and quality of life. They will then be equipped with a smart connected garment (with cardiovascular & hemodynamic sensors), a connected weight balance and a blood pressure monitoring device for telemonitoring collection of cardiovascular hemodynamic parameters in real-life conditions (for 14 days). Patients included in the registry will be followed-up for 3 years using medico-administrative databases and vital status, cardiovascular and heart failure outcomes will be collected.
Interventions
OTHERExtensive phenotyping
Prospective assessment of physical evaluation, biomarkers and omics, cardiac and vascular imaging and telemonitoring of cardiovascular parameters for 14 days.
Sponsors
BPIfrance
Sanofi
Institut de Recherches Internationales Servier
Institut National de la Santé Et de la Recherche Médicale, France
BioSerenity
Casis
Firalis SA
Fealinx
Centre National de la Recherche Scientifique, France
ESPCI Paris
University of Paris 5 - Rene Descartes
Sorbonne University
Assistance Publique - Hôpitaux de Paris
Study design
Observational model
COHORT
Time perspective
PROSPECTIVE
Eligibility
Sex/Gender
ALL
Age
18 Years to 90 Years
Healthy volunteers
Yes
Inclusion criteria
All subjects * Affiliation to a social security scheme, universal medical coverage (CMU) or any equivalent scheme * Physical state compatible with the carrying out of the investigations according to the judgment of the investigator * Procedure for obtaining consent For HFpEF patients: * Hospitalization in one of the partner hospitals in the last 30 months * With a diagnosis of symptomatic congestive heart failure (NYHA II to IV) * With a plasma concentration of BNP ≥ 100 μg / ml or NT-proBNP ≥ 300 μg / ml or having had an administration of a dose of intravenous diuretics during hospitalization for congestive heart failure * Left ventricular ejection fraction ≥ 50% * Hospital discharge for at least 2 months For HFrEF patients: * Hospitalization in one of the partner hospitals in the last 30 months * With a diagnosis of symptomatic congestive heart failure (NYHA II to IV) * Plasma concentration of BNP ≥ 100 μg / ml or NT-proBNP ≥ 300 μg / ml or administered a dose of intravenous diuretics during hospitalization for congestive heart failure * Hospital discharge for at least 2 months * Left ventricular ejection fraction ≤ 40% * Matched age and sex to HFpEF patients (for participants to extensive phenotyping) For subjects apparently without heart failure : * Subject without a notable medical history or medical history within the last 5 years * Normotensive or who may have an essential hypertension of grade 1 (≤159 / 99 mmHg), treated or not * Can present a dyslipidemia, treated by hygieno-dietetic measures alone * Sinus heart rate * Estimated glomerular filtration rate ≥ 60 ml / min (CKD epi) * Matched age and sex to HFpEF patients (for participants to extensive phenotyping)
Exclusion criteria
All subjects * Pregnancy or breastfeeding * Participation in another interventional study * Person placed under the safeguard of justice * Subject that can not understand the procedures related to the protocol * Severe obesity (BMI \> 40 Kg / m2) * For those performing the injected MRI: Patient who has already had a severe allergy to gadolinium MRI contrast agents * For those performing the injected MRI: MRI usual contraindications: Pace-maker, defibrillator, metallic objects * Administration of a vaccine dose (including anti-Sars-Cov-2) less than 3 weeks old For both HFpEF and HFrEF patients: * History of right ventricular infarction * History of cardiac transplantation or circulatory assistance * Major surgery scheduled for less than 6 months, coronary revascularization of less than 3 months * Pacemaker or any implanted device (or foreign body) not compatible with MRI * Presence of very severe co-morbidity: end-stage renal failure (GFR \<15ml / min), severe chronic obstructive pulmonary disease (COPD), severe valve disease (including severe aortic stenosis), organ transplantation * Hypertrophic cardiomyopathy of known genetic cause * Hereditary amyloidosis with disabling neuropathy * Amyloidosis under specific treatment * Other antecedent of known congenital heart disease type, Post-embolic chronic pulmonary heart, Restrictive Cardiopathy, Diagnosed Fabry Disease For HFpEF patients: \- History of systolic dysfunction with proven LVEF reduction (≤ 40%) For subjects apparently without heart failure : * Medication use other than pure systemic or local estrogen / progestin and progestin contraceptives and paracetamol, at the discretion of the investigator * Acute pathology within 8 days prior to inclusion * Cardiac or vascular organic impairment or apparent chronic diseases * Chronic treatment outside a treatment for high blood pressure * Having already had ≥3 MRI with injection of gadolinium contrast agents
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Machine learning algorithm to identify distinct phenotypic subgroups among HFpEF patients | 14 days | Machine learning-based cluster analysis using extensive phenotyping data from HFpEF, HFrEF and subjects without apparent HF |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Prognosis | 3 years | Identify phenotypic subgroup(s) with higher risk of cardiovascular and HF outcomes |
| Myocardial stiffness | 3 years | Assess the diagnostic and prognostic value of myocardial stiffness measured with ultrafast cardiac echography |
| Sarcopenia and muscular capacity | 3 years | Prevalence and importance of muscle loss, weakness measured with hand grip strength test (Kg) and with the short physical performance battery (SPPB, combining the results of gait speed, chair stand and balance tests) in HFpEF patients |
| Exercise tolerance | 3 years | Measure exercise tolerance with 6-minute walk test |
| Cardiac fibrosis | 3 years | Prevalence, diagnostic and prognostic importance of cardiac fibrosis (as estimated by cMRI and specific biological markers) in HFpEF patients |
| Arterial Stiffness | 3 years | Assess the diagnostic and prognostic value of arterial stiffness measured by pulse wave velocity |
| Right heart and pulmonary circulation | 3 years | Assess the diagnostic and prognostic value of novel markers to quantify right heart function and pulmonary circulation measured with cMRI |
| Ventricular-arterial coupling | 3 years | Machine learning-based analysis on 4D MRI recordings to estimate ventricular-arterial coupling |
| Omics signature | 3 years | Apply multi-omics techniques (including measurements of miRNA, lNcRNA, inflammation markers, and DNA methylation level) to define specific biological signatures to HF and HFpEF patients |
| Quality of life evaluation | 3 years | General and HF QOL questionnaires: Kansas city cardiomyopathy questionnaire - the sum of responses from all 12 items, Range for subscale is 0-100 and the range for the summary score is 0-100 with lower scores indicating more significant disease impact; Global quality of life score with SF36 (Short form 36 health survey): The norm data is 0-100, the health related quality of life is increased as the scores are increased. |
| Telemonitoring of weight | 3 years | Remote measurement of body weight |
| Telemonitoring of oxygen saturation | 3 years | Remote measurement of oxygen saturation (%) |
| Telemonitoring of ECG | 3 years | Remote measurement of heart rate variability |
| Telemonitoring of physical activity | 3 years | Remote measurement of physical activity with an actimeter |
| Telemonitoring of blood pressure | 3 years | Remote measurements of blood pressure in mmHg |
| Telemonitoring of pulmonary function | 3 years | Remote measurement of respiratory rate |
| Telemonitoring of pulmonary congestion | 3 years | Remote evaluation of pulmonary congestion with measurement of thoracic impedance |
| Digitalized ECG | 3 years | Develop novel machine learning based markers of HF, of HFpEF and HFrEF |
| Cardiac echography | 3 years | Rest and low-effort evaluation of cardiac parameters |
| Cardiac calcium scoring | 3 years | Evaluation of calcium scoring among participants |
| Cardiac MRI | 3 years | Novel biomarkers of cardiac fibrosis, extra-cellular volume, matrix remodeling |
| Left atria | 3 years | Evaluation of LA remodeling (volumes) and function (strain) |
| Telemonitoring of cardiac rythm | 3 years | Remote measurement of cardiac arrhythmias |
Countries
France
Outcome results
None listed