The main aim of this study is to identify the underlying mechanisms of Sodium-glucose co-transporter-2 (SGLT2) inhibitors which are associated to better outcomes in patients with Diabetes mellitus type 2 and Heart Failure with preserved Ejection Fraction.
Double design study including a clinical trial and a nested case-control study. A) Experimental study (clinical trial): Phase IV, prospective, randomized, double-blind placebo-controlled with 12 months follow-up. Inclusion criteria are: 1) diagnosis of DM2, 2) HF with preserved EF with a hospital admission in the previous 6 months with demonstration of diastolic dysfunction. 3) Stable clinical situation at inclusion. 4) Clinical indication of cardiac catheterization. Patients will be randomized 1:1 to received Dapagliflozin 10 mg/day or placebo. The main objective is to compare the impact of the drug on LV diastolic properties at the peak of effort and in levels of plasma deposit and cross-linking biomarkers of type I collagen between the two treatment groups at baseline and after 12 months. 52 patients will be recruited. B) Descriptive study: Nested case-control study, considering patients from the experimental study as cases and 10 additional patients with HF with preserved EF but no type 2 DM as controls. The main aim will be compare the histological, molecular, biochemical and biomechanical features of the HFpEF patients with and without DM2.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Enrollment
62
Dapagliflozin 10 mg / day oral
One Placebo capsule daily oral
Hospital General Universitario Gregorio Maranon
Madrid, Spain
RECRUITINGFunctional Main Objective: Impact of iSGLT2 on LV diastolic properties in terms of the change in LV stiffness constant (S+) at the peak of exercise.
Intrinsic diastolic properties will be analyzed by dynamic pressure-volume loop catheterization.
Time frame: Baseline vs 12 months
Main Structural Objective: Changes in serum levels of procollagen type I C-terminal propertied (PICP, ng/mL)
We will measure the changes in serum levels of procollagen type I C-terminal propertied (PICP, ng/mL), a validated biomarker of collagen type I deposition
Time frame: Baseline vs 12 months
Changes in LV stiffness constants (S+ and S-).
LV stiffness constants will be obtained from invasive pressure-volume data analysis.
Time frame: Baseline vs 12 months
Changes in the slope, Emax, of the end-systolic pressure-volume relationship
Emax will be obtained from invasive pressure-volume data analysis.
Time frame: Baseline vs 12 months
Impact of iSGLT2 on myocardial remodeling.
Reverse cardiac remodeling will be studied by cardiac magnetic resonance (CMR). CMR studies will be performed on 1.5 T scanners and will include short-axis cine steady-state free-precession images from base to apex, and standard long axis views for the analysis of mass, volume and ventricular function. CMR study will require the administration of a gadolinium contrast medium to study myocardial fibrosis, unless contraindicated.
Time frame: Baseline vs 12 months
Correlation of myocardial remodeling patterns with the intrinsic diastolic properties of chamber VI with systolic function.
Results from the pressure-volume analysis and CMR will be assess in common in order to search for association.
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Time frame: Baseline vs 12 months
Relative contribution of the intrinsic diastolic properties of the LV and the flow patterns on filling pressures and their modulation under treatment with iSGLT2.
Intraventricular flow patterns will be studied by Doppler echocardiography and phase contrast CMR, considering vorticity and blood transport parameters.
Time frame: Baseline vs 12 months
Changes in serum levels of collagen type I C-terminal telopeptide to matrix metalloproteinase ratio (CITP:MMP-1)
We will measure the changes in serum levels of collagen type I C-terminal telopeptide to matrix metalloproteinase ratio (CITP:MMP-1), biomarker of the degree of collagen type cross-linking.
Time frame: Baseline vs 12 months
Changes in N-terminal pro brain natriuretic peptide (pg/mL)
We will measure the changes in N-terminal pro brain natriuretic peptide (pg/mL)
Time frame: Baseline vs 12 months
Changes in high sensitivity troponin T (pg/mL)
We will measure the changes in high sensitivity troponin T (pg/mL)
Time frame: Baseline vs 12 months