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Effect of race on hypertension and antihypertensive therapy
1University of Missouri, Kansas City School of Pharmacy, USA.
Insights
Hypertension prevalence and severity differ across racial groups, with Black populations experiencing higher rates and worse outcomes. Treatment responses vary, suggesting tailored pharmacotherapy approaches are crucial for effective hypertension management.
Area of Science:
- Cardiology
- Nephrology
- Pharmacology
Background:
- Hypertension is a significant risk factor for cardiovascular and renal diseases.
- Racial background influences hypertension prevalence, pathophysiology, and treatment response.
- Black populations exhibit higher hypertension prevalence and more severe consequences, including end-stage renal disease.
Purpose of the Study:
- To review the role of race in hypertension pathogenesis and pharmacotherapy.
- To examine differential therapeutic approaches for hypertension based on racial background.
Main Methods:
- Review of existing studies, including NHANES III and HHANES.
- Analysis of factors contributing to racial differences in hypertension.
- Evaluation of treatment response data from clinical trials.
Main Results:
- Black populations have higher hypertension prevalence and worse prognosis than white populations.
- African Americans show greater responsiveness to diuretics and calcium channel blockers compared to ACE inhibitors or beta-blockers.
- Lower plasma renin activity in Black individuals may explain differential drug responses.
Conclusions:
- Racial disparities exist in hypertension prevalence, severity, and treatment response.
- Tailored pharmacotherapy, considering race-specific responses, is essential for optimal hypertension management.
- Further research into the underlying mechanisms of these disparities is warranted.
Abstract:
The presence of hypertension in individual patients confers significant risk in terms of coronary artery disease, myocardial infarction, stroke and congestive heart failure. However, it is also a modifiable risk factor, as risk may be decreased through either lifestyle changes or pharmacotherapy to reduce the elevated blood pressure. Over the past 3 decades, there has been strenuous debate among clinical scientists regarding the role played by racial background in both the pathogenesis and response to pharmacotherapy. A number of studies, such as the third National Health and Nutrition Examination Survey (NHANES III) have demonstrated a higher prevalence of hypertension in black populations. The Hispanic Health and Nutrition Examination Survey (HHANES) suggested that the prevalence of hypertension in Hispanics of Caribbean descent was similar to that of African Americans, while Mexican Americans had lower rates of the disease. It appears that the pathophysiological consequences of elevated blood pressure may also be more severe in black patients. Thus, these patients will have a worse prognosis than their white counterparts at any given blood pressure level. The incidence of end-stage renal disease has been reported to be as much as 17 times more common in African American patients. A number of individual factors have been postulated for these differences including increased sodium intake, differences in sodium handling, decreased potassium intake, decreased calcium intake, elevated fasting insulin levels, lower levels of plasma renin activity and urinary kallikrein excretion. These differences in prevalence and pathophysiology have resulted in recommendations for differential therapeutic approaches in the treatment of hypertension. A major trial conducted in the Veteran Affairs Medical Centers in the USA noted that African Americans are generally more responsive to diuretics and calcium channel blockers than to ACE inhibitors or beta-blockers. However, it has been reported that this resistance may be overcome by increasing the dose of these agents. It has been postulated that these differences may be related to lower plasma renin activity noted in the black population, since diuretics and calcium channel blockers appear to be better suited to this population. These differential therapeutic recommendations will be reviewed in light of our current knowledge of the disease.
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