Arterial Hypertension Clinical Trial
Official title:
Renal Protection Using Sympathetic Denervation in Patients With Chronic Kidney Disease (Kidney Protection Study - KPS Study)
Kidney protection study (KPS 1) is a prospective randomized clinical study comparing the use of renal denervation (RDN) and optimal medical therapy in subjects with chronic kidney disease stage 3-4 and resistant arterial hypertension to optimal medical therapy alone. Renal denervation is a modern endovascular method used to treat resistant hypertension. The method is being extended to other groups of patients, where the sympathetic tone is increased beyond resistant hypertension. Because of the character of the disease, we hypothesize that renal denervation can reduce or prevent progressive deterioration of kidney functions in this patient population. The aim of this clinical study is to show that renal denervation has protective effects on the progression of chronic renal insufficiency.
Background:
patients with chronic renal insufficiency are an ideal group for renal denervation (RDN),
because of the increase in sympathetic tone. This increase leads to sodium retention,
reduction of perfusion of the kidney and to excessive activation of renin angiotensin
aldosterone system. The activation of the sympathetic system significantly contributes to
the progression of chronic renal insufficiency. The consequences the hyperactivity of the
sympathetic system are affected by selective renal sympathectomy. RDN demonstrably reduces
retention of sodium, reduces the production of renin and significantly reduces renal
vascular resistance. Furthermore, RDN reduces microalbuminuria and renal podocyte damage in
experimental model. RDN also improves renal function in the model of acute
Glomerulonephritis. In patients with resistant hypertension and preserved renal function, it
was also shown that renal denervation improves renal resistant index and significantly
decreases microalbuminuria. The procedure was found to be safe in all studies with renal
denervation and was not associated with deterioration of renal function. Several
experimental data exist on the effectiveness of RDN in chronic renal insufficiency. In a
model of acute renal failure in mouse (endotoxemia model), it was shown that RDN has
protective effect on renal function. The decline in the glomerular filtration during
endotoxemia was significantly lower in the group treated with RDN compared to the control
group. In addition, the renal flow during acute renal failure after RDN was improved. In the
model of heart failure in mice, it has been shown that RDN in combination with olmesartan
reduces albuminuria and the damage of podocytes and also reduces the levels of renal
norepinephrine, angiotensinogen, angiotensin II, and the level of oxidative stress.
Very few data on the effect of RDN on renal function in human were also published. Renal
damage in hypertensives subject was not found after RDN with the Symplicity system more than
3 years post procedure. Mahfoud and coworkers showed that subject treated with RDN had lower
blood pressure and renal resistive index and at the same time stabilize their renal
function. The number of patients with microalbuminuria or macroalbuminuria decreased
significantly one year after RDN.
RDN has also positive effect on albuminuria and proteinuria in patients with preserved renal
function. The first studies performed in patients with chronic kidney disease (CKD stage
3-4) and resistant hypertension was done by Hering et coworkers. In this study, 15 patients
with an average eGFR of 31ml/min/1, 73m2 underwent RDN. The authors were able to show that
RDN effectively lowers blood pressure and was not associated further deterioration of renal
function. RDN had other positive effects on hemoglobin concentration , proteinuria and on
BNP levels. Moreover, the augmentation index of peripheral arteries was also improved by
RDN. This work showed multiple effects of RDN beyond the reduction of blood pressure. We,
therefore think that patient with chronic kidney disease are good candidates for RDN.
However, the mentioned study has a relatively short term follow up (6 months to one year)
and does not have a comparative arm.
Aim of study :
our proposed trial aimed to show that RDN not only contribute to improve the control of
blood pressure in patients with resistant hypertension but also has protective effects on
kidney function in subjects with chronic kidney disease. Our trial will have a comparative
arm and will last 3 years.
Planned intervention:
The two strategies that are going to be compared are optimal medical therapy against optimal
medical therapy with renal denervation.
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Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment
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