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Time to Retire Beta-Blockers in Uncomplicated Hypertension?

<ѻý class="mpt-content-deck">— Not yet, a review of the evidence suggests
MedpageToday

Beta-blockers were one of the first modern medications used for the treatment of blood pressure. Before 1950, treatment options for hypertension were limited. The alphabet soup of medications -- reserpine, pentaquine, hydralazine, and guanethidine -- were notorious for inducing orthostasis, sedation, constipation, impotence, or blurry vision. Then in the 1960s, propranolol and chlorothiazide were developed. Initially designed to treat angina pectoris, propranolol was serendipitously discovered to also lower blood pressure. Oddly, propranolol, like the other beta-blockers in its generation and thereafter, did not act directly on the blood vessel to lower blood pressure. Instead, its was via inhibition of beta-adrenergic receptors, reduction of cardiac output, and decrease in sympathetic outflow.

Despite beta-blockers' odd mechanism of action, they were (and still are) in decreasing blood pressure. Beta-blockers became extremely popular once they were found to have many fewer side effects than the older generation of drugs. Since then, many derivatives and generations of the beta-blocker have come into use and have become the mainstay in the treatment of hypertension. In the subsequent 40 years, beta-blockers battled high blood pressure in the front lines.

But in 2014, researchers appointed to the Joint National Committee on Detection, Evaluation, and Treatment of High Blood Pressure (JNC) released what was called the . In these new recommendations, beta-blockers were relegated to second-line treatment, behind thiazide diuretics, calcium channel blockers (CCB), angiotensin-converting enzyme inhibitors (ACEi), and angiotensin II receptor blockers (ARBs). After being the crux of hypertension treatment for decades, are beta-blockers becoming obsolete?

Several studies from the early 2000s rendered the beta-blocker a less attractive treatment option for hypertension. In 2002, rallying more than 30,000 hypertensive individuals, the Antihypertensive and Lipid-Lowering Treatment to Prevent Heart Attack Trial (ALLHAT) showed that treatment with the thiazide diuretic chlorthalidone decreased the rate of heart failure (HF) significantly more than an ACEi and a CCB. Additionally, African Americans treated with chlorthalidone were less likely to have a stroke. A around the same time, Intervention as a Goal in Hypertension Treatment (INSIGHT), also showed a reduction in HF rates. In contrast, these outcomes have . Thus, brought thiazide diuretics to the forefront of hypertension treatment.

A second hit befell beta-blockers in 2004, when a published in The Lancet suggested that atenolol did worse than other hypertension medications in reducing the risk of stroke (relative risk 1.13; 95% CI 1.02-1.25). Subsequent and larger confirmed this relationship, and exposed propranolol as also having this deficiency. Based on the mounting evidence, the relegated beta-blockers to second-line therapy for high blood pressure.

Several theories have been proposed to explain this observed risk of stroke. that is gaining strength is based on the idea of pulse wave dyssynchrony, whereby pressure waves are prematurely reflected back from the periphery by older and stiffer arteries, resulting in increased central systolic pressures. Because beta-blockers increase the length of systole, they exacerbate pulse wave dyssynchrony thereby increasing central aortic pressures. Using pressure sensors designed to calculate central pressures from the radial artery (called radial artery applanation tonometry), showed that not only did higher central aortic pressures lead to worse cardiovascular outcomes, but that beta-blockers were less capable of lowering central blood pressure when compared to CCBs. , in particular, could further worsen this dyssynchrony by causing relative peripheral vasoconstriction.

Keep in mind, however, that . For instance, the has shed many of the older agents' undesirable side effects, including the hyperglycemia and hyperlipidemia of the first and second generations. Moreover, beta-blockers like carvedilol and nebivolol appear to decrease peripheral vascular resistance either through alpha-1 blockade or by promoting nitric oxide (NO) release, respectively, rather than by reducing the cardiac output. These well-publicized mechanisms translated to modest reductions in central aortic pressure when compared to atenolol in . are already underway to study the blood pressure lowering effects of third-generation beta-blockers. However, further studies will be needed to examine the long-term effects of the newer beta-blockers and how they influence stroke risk, coronary heart disease outcomes, or overall mortality in uncomplicated hypertension.

Despite all the shortcomings of the beta-blocker, it is not yet time to give up on our old friend. A showed that when compared to placebo, beta-blockers have a modest effect on decreasing the risk of stroke (RR 0.80; 95% CI 0.66-0.96). Additionally, a meta-analysis in 2007 showed that most of the previously observed stroke risk was confounded by older populations. The authors were able to that this risk between beta-blockers and other antihypertensive agents was eliminated when the analysis focused on patients under 60 years old. Furthermore, most of the analyses on cardiovascular outcomes of beta-blockers were derived from studies using atenolol and propranolol and may not apply to other agents in the family. For instance, the showed that there could be a reduction in stroke and coronary heart disease when using a long-acting beta-blocker, such as metoprolol succinate. Finally, newer agents in the class with fewer metabolic side effects may become standard in our armamentarium to treat hypertension in the future. There are reasons why our counterparts up north as first-line therapy for younger patients and why they are still an appropriate option for treatment, especially in resistant hypertension.

Robin Guo, MD, is an internal medicine resident at NYU Langone Medical Center. A version of this article first appeared at , The NYU Langone Online Journal of Medicine. Full citations are available at the .