Combined olmesartan, amlodipine, and hydrochlorothiazide therapy in randomized patients with hypertension: a subgroup analysis of the TRINITY study by age
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Andrew J Lewin1, Joseph L Izzo, Michael Melino
1National Research Institute, 2010 Wilshire Blvd. Ste. 302, Los Angeles, CA 90057, USA. docl@clinical-studies.com
Insights
Triple-combination therapy with olmesartan medoxomil, amlodipine besylate, and hydrochlorothiazide effectively lowers blood pressure in both younger and older adults. This combination treatment demonstrated superior efficacy and safety compared to dual-drug regimens for hypertension management.
Area of Science:
- Cardiology
- Pharmacology
- Geriatrics
Background:
- Hypertension control remains a challenge, particularly in elderly populations.
- Older adults often experience inadequately managed high blood pressure.
Purpose of the Study:
- To assess the efficacy and safety of a triple-combination therapy (olmesartan medoxomil 40 mg/amlodipine besylate 10 mg/hydrochlorothiazide 25 mg) versus dual-combination treatments.
- To compare outcomes in participants aged <65 and ≥65 years, including a subgroup ≥75 years.
Main Methods:
- A 12-week, multicenter, double-blind, randomized, parallel-group study.
- Participants (≥18 years) with uncontrolled hypertension were randomized to four treatment arms.
- Primary endpoint was the change in seated diastolic blood pressure (SeDBP) at week 12.
Main Results:
- Triple-combination therapy significantly reduced SeDBP and seated systolic blood pressure (SeSBP) in both <65 and ≥65 age groups compared to dual therapies.
- A higher percentage of participants achieved blood pressure goals with triple-combination treatment in both age cohorts.
- The triple-combination treatment was well-tolerated, with no significant differences in adverse events between age groups.
Conclusions:
- Triple-combination therapy (olmesartan medoxomil/amlodipine besylate/hydrochlorothiazide) is a safe and effective option for managing hypertension across different age groups.
- This regimen offers superior blood pressure reduction compared to dual-combination treatments, including in elderly individuals.
Background:
Hypertension is often inadequately controlled in older people.
Objective:
This prespecified subgroup analysis assessed the efficacy and safety of an olmesartan medoxomil (OM) 40 mg/amlodipine besylate (AML) 10 mg/hydrochlorothiazide (HCTZ) 25 mg triple-combination treatment compared with the 3 components as dual-combination treatments in participants with hypertension who were <65 and ≥ 65 years of age. Within the ≥ 65 years of age subgroup, efficacy and safety were also summarized for participants ≥ 75 years of age.
Study Design:
12-week, multicenter, double-blind, randomized, parallel-group study.
Setting:
317 ambulatory care sites in the US and Puerto Rico.
Participants:
Individuals ≥ 18 years of age with mean seated blood pressure (SeBP) ≥ 140/100 or ≥ 160/90 mmHg off antihypertensive medication on 2 consecutive clinic visits with no recent history of significant cerebrovascular disease, coronary artery disease, heart failure (New York Heart Association class III or IV), severe renal insufficiency, or uncontrolled diabetes (HbA1c >9 %).
Intervention:
Participants were randomized, stratified by age, diabetes status, and race to one of four treatment assignments: OM 40/AML 10/HCTZ 25 mg, OM 40/AML 10 mg, OM 40/HCTZ 25 mg, or AML 10/HCTZ 25 mg.
Main Outcome Measure:
Least squares (LS) mean change from baseline in seated diastolic blood pressure (SeDBP) at week 12 (last observation carried forward) in each age subgroup (prespecified analysis).
Results:
Of the 2492 randomized participants in the study (total cohort), 2021 (81.1 %) were <65 and 471 (18.9 %) were ≥ 65 years of age, including 79 (3.2 %) who were ≥ 75 years of age. OM 40/AML 10/HCTZ 25 mg triple-combination treatment resulted in a significantly greater reduction in LS mean SeDBP at week 12 than dual-combination component treatments in participants in both cohorts: <65 years (21.0 vs. 14.2-17.2 mmHg; p < 0.0001) and ≥ 65 years (23.7 vs. 17.3-20.0 mmHg; p ≤ 0.002). Similarly, triple-combination treatment resulted in a greater reduction in LS mean seated systolic blood pressure (SeSBP) at week 12 than dual-combination component treatments: <65 years (38.2 vs. 28.3-31.4 mmHg; p < 0.0001) and ≥ 65 years (39.2 vs. 29.3-31.1 mmHg; p < 0.0001). Triple-combination treatment was more effective than dual-combination treatments in enabling participants to reach SeBP goal (<140/90 mmHg [<130/80 mmHg in participants with diabetes, chronic kidney disease, or chronic cardiovascular disease]) in both age subgroups (<65 years: 65 vs. 34-50 %, respectively, p < 0.0001 and ≥ 65 years: 63 vs. 32-39 %; p ≤ 0.0004). All 4 treatments were safe and well tolerated with low discontinuation rates in both age subgroups. There were no clinically relevant differences in the incidence of treatment-emergent adverse events between participants <65 and ≥ 65 years of age receiving triple-combination treatment.
Conclusion:
Triple-combination treatment with OM 40/AML 10/HCTZ 25 mg was well tolerated and more effective in lowering BP than the component dual-combination treatments in elderly and non-elderly subgroups.
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