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Published on: June 6, 2025
Strict blood-pressure control and progression of renal failure in children
Insights
Intensified blood pressure control significantly delays kidney disease progression in children. Lowering blood pressure targets, alongside ACE inhibitors, offers substantial renal protection, though proteinuria may reappear.
Area of Science:
- Pediatric Nephrology
- Cardiovascular Research
- Pharmacology
Background:
- Renal failure progression in children with chronic kidney disease (CKD) is a significant concern.
- Optimal blood pressure targets for renoprotection in pediatric CKD are not well-established.
- Angiotensin-converting-enzyme (ACE) inhibitors are used, but their role with intensified blood pressure control requires further study.
Purpose of the Study:
- To evaluate the long-term renoprotective effects of intensified blood pressure control in children with CKD receiving a fixed high dose of an ACE inhibitor.
- To compare the outcomes of intensified versus conventional blood pressure control on renal function decline and end-stage renal disease progression.
Main Methods:
- A 5-year randomized controlled trial involving 385 children (3-18 years) with CKD (GFR 15-80 ml/min/1.73 m²).
- Patients received ramipril (ACE inhibitor) and were assigned to intensified (mean arterial pressure <50th percentile) or conventional (50th-95th percentile) blood pressure control.
- Primary endpoint: 50% decline in GFR or progression to end-stage renal disease. Secondary endpoints: BP changes, GFR, and proteinuria.
Main Results:
- Intensified blood pressure control resulted in a significantly lower rate of reaching the primary endpoint (29.9% vs. 41.7%, P=0.02).
- Proteinuria initially decreased by 50% but gradually rebounded despite good blood pressure control.
- Achievement of blood pressure targets and reduced proteinuria independently predicted delayed renal disease progression.
Conclusions:
- Intensified blood pressure control, targeting low-normal 24-hour blood pressure levels, provides significant renal benefits in pediatric CKD.
- Proteinuria rebound is common during long-term ACE inhibition in children, even with controlled blood pressure.
- This study highlights the importance of aggressive blood pressure management for preserving kidney function in pediatric chronic kidney disease.
Background:
Although inhibition of the renin-angiotensin system delays the progression of renal failure in adults with chronic kidney disease, the blood-pressure target for optimal renal protection is controversial. We assessed the long-term renoprotective effect of intensified blood-pressure control among children who were receiving a fixed high dose of an angiotensin-converting-enzyme (ACE) inhibitor.
Methods:
After a 6-month run-in period, 385 children, 3 to 18 years of age, with chronic kidney disease (glomerular filtration rate of 15 to 80 ml per minute per 1.73 m(2) of body-surface area) received ramipril at a dose of 6 mg per square meter of body-surface area per day. Patients were randomly assigned to intensified blood-pressure control (with a target 24-hour mean arterial pressure below the 50th percentile) or conventional blood-pressure control (mean arterial pressure in the 50th to 95th percentile), achieved by the addition of antihypertensive therapy that does not target the renin-angiotensin system; patients were followed for 5 years. The primary end point was the time to a decline of 50% in the glomerular filtration rate or progression to end-stage renal disease. Secondary end points included changes in blood pressure, glomerular filtration rate, and urinary protein excretion.
Results:
A total of 29.9% of the patients in the group that received intensified blood-pressure control reached the primary end point, as assessed by means of a Kaplan-Meier analysis, as compared with 41.7% in the group that received conventional blood-pressure control (hazard ratio, 0.65; confidence interval, 0.44 to 0.94; P=0.02). The two groups did not differ significantly with respect to the type or incidence of adverse events or the cumulative rates of withdrawal from the study (28.0% vs. 26.5%). Proteinuria gradually rebounded during ongoing ACE inhibition after an initial 50% decrease, despite persistently good blood-pressure control. Achievement of blood-pressure targets and a decrease in proteinuria were significant independent predictors of delayed progression of renal disease.
Conclusions:
Intensified blood-pressure control, with target 24-hour blood-pressure levels in the low range of normal, confers a substantial benefit with respect to renal function among children with chronic kidney disease. Reappearance of proteinuria after initial successful pharmacologic blood-pressure control is common among children who are receiving long-term ACE inhibition. (ClinicalTrials.gov number, NCT00221845.)
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