Heart failure (HF) currently affects app. 2% of the western population and app. 10% of people \>75 years. In about 50% of patients with symptomatic HF ejection fraction (EF) is preserved (HF-PEF). Once patients develop symptoms, the prognosis is poor with 25% mortality at 1 year and 50% mortality at 5 years. HFpEF is one of the major unresolved areas in clinical cardiology. The diagnosis of HFpEF remains a diagnosis of exclusion and currently no non-invasive measure provides a clear diagnosis. Cardiovascular magnetic resonance (CMR) provides non invasive and radiation free evaluation of heart structure and function. New CMR parameters offer the possibility to describe the underlying pathological and physiological changes associated with HFpEF. The investigators propose to undertake the first systematic comparison between a CMR protocol and invasive haemodynamics as the best possible gold standard, as well as define the histopathological drivers in myocardial biopsies. The investigators will also examine the relations with tissue and serological biomarkers implicated in HFpEF and the role with standard and novel parameters by echocardiography. If successful, this study will provide tools for a reliable and accurate non-invasive characterization of patients with HFpEF, supporting the diagnosis and grading the severity of disease. This study will provide a reference basis for future diagnostic algorithms in HFpEF, both, for CMR and echocardiography, but also for their relative value in comparison to blood markers or invasive testing. In addition to a new pathway to acess the effects of current and novel therapeutic interventions, the investigators see the greatest potential in identifying a disease stage where the myocardial injury may be reversible.
Study Type
OBSERVATIONAL
Enrollment
185
Cardiovascular magnetic resonance (CMR) provides non-invasive, radiation-free and in-depth evaluation of myocardial structure and function. In addition to established tools for assessment of cardiac volume, mass, function and regional myocardial scar with late Gadolinium enhancement (LGE), several novel quantitative CMR parameters will be assessed including T1-mapping or fully quantitative perfusion Imaging.
Blood samples will eventually be analysed for markers related to heart failure (BNP/NT)-pro-BNP, myocardial inflammation and fibrosis (cytokine profiling, Galectin-3, Procollagen Type I and III, hsCRP). Whole blood will be frozen for DNA isolation and genome analysis. Peripheral blood mononuclear cells will be isolated by Ficoll in a subset of patients and will be used for RNA isolation allowing RNA-seq or reverse transcription (RT) - polymerase chain reaction (PCR) analysis.
Measurements will include cavity dimensions, flow velocities, myocardial motion velocity and strain as well as for change of parameters during ergometric stress.
Multiple parameters (including EDPVR, ESPVR, dp/dt min, Tau, Ea) will be derived from the various PV loop assessments and additional relevant parameters will be calculated. Right ventricular and pulmonary pressures including pulmonary vascular resistance will be measured with Swan-Ganz catheters using right venous femoral approach.
A set of myocardial biopsies for each patient will be stained with Masson Trichrome for qualitative and quantitative assessment of the collagen volume fraction; fat droplets will be identified by red oil staining, Congo Red for amyloid immunohistology will be used to determine total leukocytes (CD45), T-cells (CD3) and monocytes/macrophages (CD68). A second set of biopsies will be frozen immediately and stored at -80°. Western blot analysis will be performed to determine alterations at the myofilament level including titin isoform composition and phosphorylation status.
University Hospital Frankfurt
Frankfurt am Main, Hesse, Germany
Kerckhoff Klinik
Bad Nauheim, Germany
Charite Centrum Herz-, Kreislauf- und Gefäßmedizin
Berlin, Germany
University Hospital Göttingen
Göttingen, Germany
University Hospital
Heidelberg, Germany
Herzzentrum Leipzig
Leipzig, Germany
Uniersity Hospital Mainz
Mainz, Germany
Significant influence of MR Imaging Parameters on a multivariate model to describe the invasive pressure volume relations (EDPVR).
Using a multivariable regression analysis and a respective F test.
Time frame: up to 4 weeks. No follow up is planned.
Association between CMR T1-mapping and biopsy results.
Using suitable regression and correlation Analysis.
Time frame: up to 4 weeks. No follow up is planned.
Association between CMR flow echocardiographic flow
Using suitable regression and correlation Analysis.
Time frame: up to 4 weeks. No follow up is planned.
Association between a model for diastolic function based on CMR with a model of diastolic function based on echocardiography
Using suitable regression and correlation Analysis.
Time frame: up to 4 weeks. No follow up is planned.
Association between CMR function and echocardiographic function
Using suitable regression and correlation Analysis.
Time frame: up to 4 weeks. No follow up is planned.
Discriminatory capacity of a multivariate model of invasive and a multivariate model of non-invasive variables.
Using the patient and control groups with comparative ROC analysis and DeLong tests.
Time frame: up to 4 weeks. No follow up is planned.
Reproducibility at one site.
Using respective intra-class correlations in the groups with multiple measurements.
Time frame: up to 4 weeks. No follow up is planned.
Variability between the different sites.
Using respective intra-class correlations in the groups with multiple measurements.
Time frame: up to 4 weeks. No follow up is planned.
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