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Systolic blood pressure variability as a risk factor for stroke and cardiovascular mortality in the elderly
Edward Pringle1, Charles Phillips, Lutgarde Thijs
1Royal Sussex County Hospital, Brighton, UK.
Insights
Increased night-time systolic blood pressure variability is a stroke risk factor in elderly hypertensive individuals not on active treatment. Antihypertensive therapy may mitigate this risk.
Area of Science:
- Cardiology
- Hypertension Research
- Clinical Trials
Background:
- Systolic blood pressure variability (SBPV) is a potential predictor of cardiovascular events.
- The Syst-Eur trial investigated antihypertensive treatment in elderly Europeans.
Purpose of the Study:
- To determine if baseline SBPV predicts stroke, cardiovascular mortality, or cardiac events in the Syst-Eur trial.
- To assess the impact of antihypertensive treatment on SBPV and its predictive value.
Main Methods:
- A randomized, double-blind, placebo-controlled trial (Syst-Eur) involving 744 elderly hypertensive participants.
- SBPV measured at baseline over 24 hours, daytime, and night-time.
- Intention-to-treat analysis using Cox regression, adjusting for confounders.
Main Results:
- A 5 mmHg increase in night-time SBPV correlated with an 80% higher stroke risk in the placebo group.
- Daytime SBPV did not predict outcomes.
- Antihypertensive treatment did not alter SBPV during the median 4.4-year follow-up.
Conclusions:
- Elevated night-time SBPV at baseline independently predicted stroke in the placebo group of the Syst-Eur trial.
- This association was not observed in the active treatment group, suggesting a potential protective effect of antihypertensive therapy.
Objective:
To investigate whether baseline systolic blood pressure variability was a risk factor for stroke, cardiovascular mortality or cardiac events during the Syst-Eur trial.
Design:
The Syst-Eur study was a randomized, double-blind, placebo-controlled trial, powered to detect differences in stroke rate between participants on active antihypertensive treatment and placebo. Systolic blood pressure variability measurements were made on 744 participants at the start of the trial. Systolic blood pressure variability was calculated over three time frames: 24 h, daytime and night-time. The placebo and active treatment subgroups were analysed separately using an intention-to-treat principle, adjusting for confounding factors using a multiple Cox regression model.
Participants:
An elderly hypertensive European population.
Main Outcome Measures:
Stroke, cardiac events (fatal and non-fatal heart failure, fatal and non-fatal myocardial infarction and sudden death) and cardiovascular mortality (death attributed to stroke, heart failure, myocardial infarction, sudden death, pulmonary embolus, peripheral vascular disease and aortic dissection).
Results:
The risk of stroke increased by 80% (95% confidence interval: 17-176%) for every 5 mmHg increase in night-time systolic blood pressure variability in the placebo group. Risk of cardiovascular mortality and cardiac events was not significantly altered. Daytime variability readings did not predict outcome. Antihypertensive treatment did not affect systolic blood pressure variability over the median 4.4-year follow-up.
Conclusion:
In the placebo group, but not the active treatment group, increased night-time systolic blood pressure variability on admission to the Syst-Eur trial was an independent risk factor for stroke during the trial.
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