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Relation of beta-blocker-induced heart rate lowering and cardioprotection in hypertension
Sripal Bangalore1, Sabrina Sawhney, Franz H Messerli
1Department of Medicine, Division of Cardiology, St Luke's Roosevelt Hospital, Columbia University College of Physicians and Surgeons, New York, New York 10019, USA.
Insights
Beta-blockers lower heart rate in hypertension patients, but this reduction paradoxically increases cardiovascular risks. This contrasts with benefits seen in heart failure and post-myocardial infarction patients.
Area of Science:
- Cardiology
- Pharmacology
- Hypertension Research
Background:
- Elevated resting heart rate is a known cardiovascular risk factor in the general population and in patients with conditions like hypertension.
- Pharmacological heart rate reduction is generally beneficial for individuals with existing heart disease.
- The specific impact of beta-blockers on heart rate and cardiovascular event risk in hypertensive patients remains unclear.
Purpose of the Study:
- To investigate the effect of heart rate reduction achieved with beta-blockers on the risk of cardiovascular events in patients diagnosed with hypertension.
Main Methods:
- A comprehensive literature search was conducted across MEDLINE, EMBASE, and CENTRAL databases for studies published from 1966 to May 2008.
- Included were randomized controlled trials (RCTs) using beta-blockers as a primary hypertension treatment, with a minimum one-year follow-up and available heart rate data.
- Data extracted included baseline characteristics, blood pressure response, heart rate changes, and cardiovascular outcomes.
Main Results:
- Analysis of 9 RCTs involving 34,096 patients on beta-blockers, 30,139 on other antihypertensives, and 3,987 on placebo revealed a concerning trend.
- A lower heart rate at study conclusion in the beta-blocker group was paradoxically associated with increased risks of all-cause mortality, cardiovascular mortality, myocardial infarction, and heart failure.
- This association persisted when comparing heart rate differences with relative risk reduction for cardiovascular events.
Conclusions:
- Unlike patients with myocardial infarction or heart failure, hypertensive patients experiencing beta-blocker-induced heart rate reduction showed an elevated risk of cardiovascular events and mortality.
- These findings challenge the universal application of heart rate reduction as a sole therapeutic goal in hypertension management.
Objectives:
The purpose of this study was to evaluate the role of heart rate reduction with beta-blockers on the risk of cardiovascular events in patients with hypertension.
Background:
Resting heart rate has been shown to be a risk factor for cardiovascular morbidity and mortality in the general population and in patients with heart disease such as hypertension, myocardial infarction, and heart failure. Conversely, pharmacological reduction of heart rate is beneficial for patients with heart disease. However, the role of pharmacological reduction of heart rate using beta-blockers in preventing cardiovascular events in patients with hypertension is not known.
Methods:
We conducted a MEDLINE/EMBASE/CENTRAL database search of studies from 1966 to May 2008. We included randomized controlled trials that evaluated beta-blockers as first-line therapy for hypertension with follow-up for at least 1 year and with data on heart rate. We extracted the baseline characteristics, the blood pressure response, heart rate at the baseline and end of trial, and cardiovascular outcomes from each trial.
Results:
Of 22 randomized controlled trials evaluating beta-blockers for hypertension, 9 studies reported heart rate data. The 9 studies evaluated 34,096 patients taking beta-blockers against 30,139 patients taking other antihypertensive agents and 3,987 patients receiving placebo. Paradoxically, a lower heart rate (as attained in the beta-blocker group at study end) was associated with a greater risk for the end points of all-cause mortality (r = -0.51; p < 0.0001), cardiovascular mortality (r = -0.61; p < 0.0001), myocardial infarction (r = -0.85; p < 0.0001), stroke (r = -0.20; p = 0.06), or heart failure (r = -0.64; p < 0.0001). The same was true when the heart rate difference between the 2 treatment modalities at the end of the study was compared with the relative risk reduction for cardiovascular events.
Conclusions:
In contrast to patients with myocardial infarction and heart failure, beta-blocker-associated reduction in heart rate increased the risk of cardiovascular events and death for hypertensive patients.
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