Cardiovascular (CV) pathologies are the leading cause of death in kidney transplant patients.Arterial stiffness is a prognostic factor for CV mortality in kidney transplantation. Despite a reduced CV risk in transplant kidney patients in comparison to patients in dialysis, CV mortality among kidney transplant patients is much higher than the general population. After renal transplantation, the cardiac and vascular anomalies observed in chronic end-stage renal disease are partially improved because of restored normal kidney function and withdrawal from dialysis. However, patients are exposed to immunosuppressive drugs, in particular calcineurin inhibitors, which can be associated with vascular toxicity, either directly or by promoting the appearance of hypertension, diabetes, or dyslipidemia.The pathophysiology of arterial stiffness in kidney transplantation is complex and multifactorial. Calcineurin inhibitors are likely to play an important role in the persistence of increased arterial stiffness in transplant patients in whom renal function has been restored. Indeed, the discontinuation of anti-calcineurins in favour of other molecules .is associated with a decrease of arterial stiffness. Preclinical work has shown that the vascular toxicity of cyclosporine is mediated by activation of the mineralocorticoid receptor in smooth muscle cells. The involvement of the mineralocorticoid receptor in the onset of arterial stiffness is also well demonstrated in non-transplanted subjects. Blocking the mineralocorticoid receptor in patients under cyclosporine may reduce their arterial stiffness and in and consequently improve their CV prognosis. Studies have show a good safety in kidney transplant patients. This pilot study proposes to examine, for the first time, the impact of treatment with a mineralocorticoid receptor antagonist on the evolution of arterial stiffness in renal transplant patients on calcineurin inhibitors.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
36
Eplerenone 50mg/day for 6 months followed
6-month period without eplerenone
CHRU de Nancy
Vandœuvre-lès-Nancy, France
RECRUITINGEvolution of pulse wave velocity (PWV in m/s) adjusted to the blood pressure
Time frame: After 6 months of treatment with eplerenone
Evolution of Central Systolic Blood Pressure (CSPc)
Time frame: After 6 months of treatment with eplerenone
Evolution of central Diastolic Blood Pressure (CDAb)
Time frame: After 6 months of treatment with eplerenone
Evolution of Central Pulsed Pressure (CPp)
Time frame: After 6 months of treatment with eplerenone
Evolution of Augmentation index (Aix in %)
Time frame: After 6 months of treatment with eplerenone
Evolution peripheral systolic blood pressure (PASp in mmHg)
Time frame: After 6 months of treatment with eplerenone
Evolution of peripheral diastolic blood pressure (PADp in mmHg)
Time frame: After 6 months of treatment with eplerenone
Evolution of peripheral pulse pressure (PPp in mmHg)
Time frame: After 6 months of treatment with eplerenone
Evolution of Intima-media thickness (in mm)
Time frame: After 6 months of treatment with eplerenone
Evolution of left ventricular mass (LVM in g/m2)
Time frame: After 6 months of treatment with eplerenone
Evolution of biological markers of oxidative stress (plasma Isoprostane)
Time frame: After 6 months of treatment with eplerenone
Evolution of biological markers of oxidative stress (Malondialdehyde)
Time frame: After 6 months of treatment with eplerenone
Evolution of Biological markers of endothelial dysfunction (endothelin)
Time frame: After 6 months of treatment with eplerenone
Evolution of biological markers of endothelial dysfunction (soluble endothelium selectin (sE-selectin))
Time frame: After 6 months of treatment with eplerenone
Evolution of biological markers of endothelial dysfunction (von Willebrand factor)
Time frame: After 6 months of treatment with eplerenone
Evolution of graft function
measured by creatinine (in micromol/L) with estimation of glomerular filtration rate (eGFR in mL/min/1.73m2 ) according to the CKD-EPI formula.
Time frame: After 6 months of treatment with eplerenone
Evolution of proteinuria
measured by the ratio proteinuria/creatinuria (in mg/g)
Time frame: After 6 months of treatment with eplerenone
Percentage of patients with DFG ≥ 90, 60-89, 45-59, 30-44, 15-29 <15ml/min/1,73m2
Time frame: After 6 months of treatment with eplerenone
Percentage of patient with ratio proteinuria/creatinuria (en mg/g) <500 ; 500-1000, 1000-2000, 2000-3000, >3000
Time frame: After 6 months of treatment with eplerenone
hyperkalemia occurence ≥ 5.5 mmol/L
Time frame: during 6 month of treatment with eplerenone
Number of hyperkalemia
number of hyperkalemias during hyperkalemia follow-up between 5 - 5.49; 5.5 - 6; \>6mmol/L
Time frame: during 6 month of treatment with eplerenone
increase of creatinine of more than 50%
Evaluation of risk of acute renal failure defined as an increase in creatinine of more than 50%
Time frame: during 6 month of treatment with eplerenone
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