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Intensive blood pressure lowering in different age categories: insights from the Systolic Blood Pressure Intervention
Christina Byrne1, Manan Pareek2,3,4, Muthiah Vaduganathan2
1Department of Cardiology, The Heart Centre, Rigshospitalet - Copenhagen University Hospital, Blegdamsvej 9, 2100 Copenhagen Ø, Denmark.
Insights
Intensive blood pressure lowering is safe and effective across all adult age groups. The Systolic Blood Pressure Intervention Trial (SPRINT) found no age-related differences in benefits or risks for hypertension management.
Area of Science:
- Cardiology
- Gerontology
- Clinical Trials
Background:
- The 2018 ESC/ESH hypertension guidelines suggest age-specific management strategies for patients under 65, 65-79, and 80+ years.
- It remains uncertain if intensive blood pressure lowering is equally safe and effective across different age groups.
Purpose of the Study:
- To evaluate whether the efficacy and safety of intensive versus standard antihypertensive treatment in the SPRINT trial are modified by patient age.
Main Methods:
- The SPRINT trial randomized 9361 high-risk adults (age ≥50) to intensive or standard blood pressure targets.
- Age-related efficacy and safety were assessed using Cox proportional-hazards regression and restricted cubic splines.
- Participants were categorized as <65, 65-79, and ≥80 years.
Main Results:
- Age was associated with stroke risk (linear) and other adverse events (non-linear).
- However, the benefits and risks of intensive blood pressure lowering did not significantly differ across age groups (P > 0.05).
- Mean age was comparable between intensive and standard treatment groups (67.9 years).
Conclusions:
- The SPRINT trial demonstrates that intensive blood pressure lowering is not modified by age in terms of safety or efficacy.
- These findings suggest that the benefits and risks of intensive antihypertensive treatment are consistent across the adult age spectrum, contrary to some guideline recommendations.
Aims:
The 2018 ESC/ESH guidelines for hypertension recommend differential management of patients who are <65, 65-79, and ≥80 years of age. However, it is unclear whether intensive blood pressure lowering is well-tolerated and modifies risk uniformly across the age spectrum.
Methods And Results:
SPRINT randomized 9361 high-risk adults without diabetes and age ≥50 years with systolic blood pressure 130-180 mmHg to either intensive or standard antihypertensive treatment. The primary efficacy endpoint was the composite of acute coronary syndromes, stroke, heart failure, or death from cardiovascular causes. The primary safety endpoint was composite serious adverse events. We assessed whether age modified the efficacy and safety of intensive vs. standard blood pressure lowering using Cox proportional-hazards regression and restricted cubic splines. In all, 3805 (41%), 4390 (47%), and 1166 (12%) were <65, 65-79, and ≥80 years. Mean age was similar between the two study groups (intensive group 67.9 ± 9.4 years vs. standard group 67.9 ± 9.5 years; P = 0.94). Median follow-up was 3.3 years. In multivariable models, age was linearly associated with the risk of stroke (P < 0.001) and non-linearly associated with the risk of primary efficacy events, death from cardiovascular causes, death from any cause, heart failure, and serious adverse events (P < 0.001). The safety and efficacy of intensive blood pressure lowering were not modified by age, whether tested continuously or categorically (P > 0.05).
Conclusion:
In SPRINT, the benefits and risks of intensive blood pressure lowering did not differ according to the age categories proposed by the ESC/ESH guidelines for hypertension.
Trial Registration:
SPRINT (Systolic Blood Pressure Intervention Trial); ClinicalTrials.gov Identifier: NCT01206062, https://clinicaltrials.gov/ct2/show/NCT01206062.
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