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Redefining beta-blocker use in hypertension: selecting the right beta-blocker and the right patient
1NY Presbyterian Hospital-Weill Cornell medicine, New York, USA.
Insights
Beta-blockers are often overused for hypertension. This perspective argues for targeted use in specific patients, particularly those with neurogenic hypertension, and suggests combined alpha/beta-blockers may offer advantages.
Area of Science:
- Cardiology
- Pharmacology
- Hypertension Management
Background:
- Randomized controlled trials indicate traditional beta-blockers are inferior for initial hypertension treatment compared to other drug classes.
- Beta-blocker use is linked to adverse effects, leading some guidelines to deem them less suitable for first-line therapy.
- Despite evidence, beta-blockers remain widely prescribed and potentially overused in hypertension management.
Purpose of the Study:
- To advocate for a more targeted approach to beta-blocker use in hypertension.
- To identify specific patient profiles and hypertension mechanisms where beta-blockers are most effective.
- To highlight the potential benefits of combined alpha/beta-blockers and specific pharmacokinetic properties.
Main Methods:
- Review of existing randomized controlled trials and clinical guidelines on hypertension treatment.
- Analysis of hypertension pathophysiology to delineate appropriate beta-blocker patient selection.
- Evaluation of different beta-blocker subclasses, including combined alpha/beta-blockers and pharmacokinetic considerations.
Main Results:
- Beta-blockers are generally ineffective for sodium/volume-mediated or renin-angiotensin system-mediated hypertension.
- They are best suited for sympathetically driven (neurogenic) hypertension, as first-line or add-on therapy.
- Combined alpha/beta-blockade and non-lipophilic beta-blockers with favorable pharmacokinetics show promise.
Conclusions:
- Beta-blockers have a valuable role in hypertension but require precise patient and drug selection.
- Targeting neurogenic hypertension and considering pharmacokinetic profiles can optimize beta-blocker effectiveness.
- Further research into combined alpha/beta-blockers and specific beta-blocker formulations is warranted.
Abstract:
Randomized controlled trials have concluded that the cardiovascular outcome of first-step treatment of hypertension with traditional vasoconstricting beta-blockers is inferior to treatment with other antihypertensive drug classes. Beta-blocker use is also associated with undesirable side effects. Consequently, some recent guidelines consider beta-blockers an inferior option for first-step treatment of hypertension. Despite this, beta-blockers are still widely prescribed, and likely overused, in the management of hypertension. It is the contention of this perspective that beta-blockers do have an important role in treating hypertension, but their use needs to be much better targeted, by better identification of both the right patient and the right beta-blocker. Identifying the right patient involves consideration of underlying mechanisms of hypertension. In the absence of comorbidities for which a beta-blocker is indicated, beta-blockers would not seem to be the preferred treatment for patients with either sodium/volume-mediated hypertension, for which they are usually ineffective, or for those with renin-angiotensin system-mediated hypertension, for which angiotensin-converting enzyme inhibitors and angiotensin receptor blockers provide equal antihypertensive efficacy with evidence of better outcome and fewer adverse effects. Beta-blockers would instead appear to be best suited for patients with sympathetically driven, that is, neurogenic, hypertension, whether as a first-step drug, such as in patients with hypertension in the acute post-stroke period, in so-called "hyperkinetic" patients, and in patients with labile hypertension, or as an add-on drug in patients with resistant hypertension. In choosing among the beta-blockers, combined alpha/beta-blockade offers advantages over beta-blocker monotherapy and merits greater clinical and research attention. Finally, unreliable bioavailability greatly interferes with the effectiveness of lipophilic, but not nonlipophilic, beta-blockers. Clinical effectiveness could be improved with greater focus on the beta-blockers with the more favorable pharmacokinetics.
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