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Updated: May 5, 2026

Assessment of Vascular Function in Patients With Chronic Kidney Disease
Published on: June 16, 2014
Intensive blood-pressure control in hypertensive chronic kidney disease
Lawrence J Appel1, Jackson T Wright, Tom Greene
1Welch Center for Prevention, Epidemiology, and Clinical Research, Johns Hopkins Medical Institutions, Baltimore, MD 21205-2223, USA. lappel@jhmi.edu
Insights
Intensive blood pressure control did not slow kidney disease progression in black patients overall. However, it may benefit those with significant baseline proteinuria.
Area of Science:
- Nephrology
- Cardiovascular Medicine
- Clinical Trials
Background:
- Hypertension and end-stage renal disease (ESRD) share a direct, progressive relationship.
- Black patients bear a disproportionately high burden of hypertension-related chronic kidney disease (CKD) and ESRD.
- Limited trials have investigated intensive blood pressure control's efficacy in slowing CKD progression in this demographic.
Purpose of the Study:
- To evaluate the effect of intensive blood pressure control on CKD progression in black patients.
- To determine if baseline proteinuria influences the efficacy of intensive blood pressure control.
Main Methods:
- Randomized trial of 1094 black patients with hypertensive CKD assigned to intensive or standard blood pressure control.
- Follow-up included a trial phase and a subsequent cohort phase with a target BP < 130/80 mm Hg.
- Primary outcome: CKD progression (doubled creatinine, ESRD, or death), with 8.8–12.2 years of follow-up.
Main Results:
- No significant difference in primary outcome between intensive and standard BP control groups overall (HR, 0.91; P=0.27).
- Mean BP was 130/78 mm Hg (intensive) vs. 141/86 mm Hg (standard) in trial phase.
- Mean BP was 131/78 mm Hg (intensive) vs. 134/78 mm Hg (standard) in cohort phase.
- Significant interaction with baseline proteinuria (P=0.02); intensive control showed potential benefit for proteinuria > 0.22 (HR, 0.73; P=0.01).
Conclusions:
- Intensive blood pressure control did not significantly impact overall kidney disease progression in this cohort.
- Potential differential benefits of intensive BP control may exist for patients with higher baseline proteinuria.
- Further research is warranted to explore targeted BP management strategies based on proteinuria levels.
Background:
In observational studies, the relationship between blood pressure and end-stage renal disease (ESRD) is direct and progressive. The burden of hypertension-related chronic kidney disease and ESRD is especially high among black patients. Yet few trials have tested whether intensive blood-pressure control retards the progression of chronic kidney disease among black patients.
Methods:
We randomly assigned 1094 black patients with hypertensive chronic kidney disease to receive either intensive or standard blood-pressure control. After completing the trial phase, patients were invited to enroll in a cohort phase in which the blood-pressure target was less than 130/80 mm Hg. The primary clinical outcome in the cohort phase was the progression of chronic kidney disease, which was defined as a doubling of the serum creatinine level, a diagnosis of ESRD, or death. Follow-up ranged from 8.8 to 12.2 years.
Results:
During the trial phase, the mean blood pressure was 130/78 mm Hg in the intensive-control group and 141/86 mm Hg in the standard-control group. During the cohort phase, corresponding mean blood pressures were 131/78 mm Hg and 134/78 mm Hg. In both phases, there was no significant between-group difference in the risk of the primary outcome (hazard ratio in the intensive-control group, 0.91; P=0.27). However, the effects differed according to the baseline level of proteinuria (P=0.02 for interaction), with a potential benefit in patients with a protein-to-creatinine ratio of more than 0.22 (hazard ratio, 0.73; P=0.01).
Conclusions:
In overall analyses, intensive blood-pressure control had no effect on kidney disease progression. However, there may be differential effects of intensive blood-pressure control in patients with and those without baseline proteinuria. (Funded by the National Institute of Diabetes and Digestive and Kidney Diseases, the National Center on Minority Health and Health Disparities, and others.)
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