Key result
Combination therapy with amlodipine/benazepril resulted in significantly greater lowering of blood pressure than monotherapy (p<0.001), with the high-dose 10/40 mg/day combination achieving similar reductions in both Black and White patients.
Why the study?
Does amlodipine/benazepril combination therapy reduce blood pressure in Black and White hypertensive patients not controlled on monotherapy compared to monotherapy?
Does amlodipine/benazepril combination therapy reduce blood pressure in Black and White hypertensive patients not controlled on monotherapy compared to monotherapy?
p-value: p=<0.001
High-dose amlodipine/benazepril combination therapy effectively lowers blood pressure in both Black and White hypertensive patients not controlled on monotherapy, overcoming the racial disparity in response seen with lower doses.
May address racial BP response gaps in uncontrolled hypertension; leaves open outcome benefits versus monotherapy in diverse populations.
BACKGROUND: Black hypertensive patients are more resistant to angiotensin-converting enzyme (ACE) inhibitor monotherapy than White patients. This resistance can be overcome with the combination of ACE inhibitors with diuretics or calcium-channel blockers (CCBs). OBJECTIVES: The objective of this clinical investigation was to evaluate the antihypertensive effectiveness of monotherapy with the ACE inhibitor benazepril or the CCB amlodipine and their combination in Black and White hypertensive patients in two separate studies. METHODS: This was a post hoc analysis of data from two separate studies, pooled because of their similarities, to increase the sample size. Outpatient Black and White hypertensive patients were selected for these studies. In study H2303, 201 patients of both sexes and races, whose mean seated diastolic blood pressure (MSDBP) was ≥95 mmHg after 4 weeks of single-blind treatment with benazepril 40 mg/day, were randomized into two groups. Group 1 received benazepril 40 mg/day and group 2 received amlodipine/benazepril 5/40 mg/day, which was uptitrated to amlodipine/benazepril 10/40 mg/day at week 4 of the study. In study H2304, 812 similar patients, whose MSDBP was ≥95 mmHg after 4 weeks of single-blind treatment with amlodipine 10 mg/day, were randomized into three groups. Group 1 received amlodipine/benazepril 10/20 mg/day, uptitrated to amlodipine/benazepril 10/40 mg/day after 2 weeks. Group 2 received amlodipine/benazepril 10/20 mg/day. Group 3 received amlodipine 10 mg/day. All three groups were followed up for 6 additional weeks. RESULTS: This report presents the results of post hoc analysis of pooled data from two separate but similar studies. Combination therapy resulted in greater lowering of MSDBP and mean seated systolic blood pressure (MSSBP) than monotherapy with either benazepril or amlodipine (p < 0.001). With respect to combination therapy, the combination of amlodipine/benazepril 10/20 mg/day resulted in greater blood pressure (BP) reductions in White patients than in Black patients (p < 0.004). In contrast, the combination of amlodipine/benazepril 10/40 mg/day resulted in similar BP reductions in both Black and White hypertensive patients. There were no serious clinical or metabolic side effects noted, with the exception of pedal edema, which was more common with amlodipine monotherapy. CONCLUSION: This study showed that combination therapy with amlodipine/benazepril is more effective in BP lowering than monotherapy with the component drugs. Black hypertensive patients are responsive to the combination of amlodipine/benazepril; however, they require higher dose combinations for BP reductions similar to those achieved in White hypertensive patients.
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Steven G. Chrysant (2012) studied Hypertension not controlled on monotherapy (n=1,141). Amlodipine/benazepril combination vs. Benazepril 40 mg/day or amlodipine 10 mg/day monotherapy was evaluated on Reduction in mean seated diastolic blood pressure (MSDBP) and mean seated systolic blood pressure (MSSBP) (p=<0.001). Combination therapy with amlodipine/benazepril resulted in significantly greater lowering of blood pressure than monotherapy (p<0.001), with the high-dose 10/40 mg/day combination achieving similar reductions in both Black and White patients.
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