Key result
Aldosterone synthase inhibitors like baxdrostat reduce BP in essential and resistant hypertension by selectively decreasing aldosterone.
Why the study?
Existing antihypertensive therapies and low-sodium diets often fail to adequately control blood pressure due to compensatory RAAS upregulation, prompting a review of novel aldosterone synthase inhibitors.
Do aldosterone synthase inhibitors reduce blood pressure and aldosterone levels in patients with hypertension?
Systematic Review
Do aldosterone synthase inhibitors reduce blood pressure and aldosterone levels in patients with hypertension?
Aldosterone synthase inhibitors represent a promising novel therapeutic class for the treatment of essential and resistant hypertension by selectively targeting aldosterone production without the compensatory RAAS upregulation seen with traditional therapies.
Supports aldosterone synthase inhibitors for resistant hypertension; extends RAAS blockade evidence to direct synthase inhibition.
Systemic hypertension (HTN) is the hallmark of cardiovascular disease and the forerunner of heart failure. These associations have been established over decades of research on essential HTN. Advancements in the treatment of patients diagnosed with HTN, consisting of alpha- or beta-adrenergic receptor blockers, calcium channel blockers, angiotensin-converting enzyme inhibitors, thiazide, or aldosterone receptor blockers known as anti-mineralocorticoids, in the presence or absence of low sodium salt diets, often fail to control blood pressure adequately to prevent morbidity and mortality. Low sodium diets have had limited success in controlling HTN because low sodium intake is associated with renin-angiotensin-aldosterone system upregulation. Therefore, upregulating aldosterone secretion, sodium, and water retention which, in turn, moves the blood pressure back toward the range of HTN dictated by the baroreceptor reset value, as a compensatory mechanism, especially in resistant HTN. These impediments to blood pressure control in HTN may have been effectively circumvented by the advent of a new class of drugs known as aldosterone synthase inhibitors, represented by baxdrostat. The mechanism of action of baxdrostat as an aldosterone synthase inhibitor demonstrates the inextricable linkage between sodium and blood pressure regulation. Theoretically, combining a low sodium diet with the activity of this aldosterone synthesis inhibitor should alleviate the adverse effect of renin-angiotensin-aldosterone system upregulation. Aldosterone synthesis inhibition should also decrease the oxidative stress and endothelial dysfunction associated with HTN, causing more endothelial nitric oxide synthesis, release, and vasorelaxation. To the best of our knowledge, this is the first systematic review to summarize evidence-based articles relevant to the use of a novel drug (aldosterone synthase inhibitor) in the treatment of HTN and cardiovascular disease. Making the current database of relevant information on baxdrostat and other aldosterone synthase inhibitors readily available will, no doubt, aid physicians and other medical practitioners in their decision-making about employing aldosterone synthase inhibitors in the treatment of patients.
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Awosika et al. (2023) conducted a systematic review in Systemic hypertension and resistant hypertension. Aldosterone synthase inhibitors (LCI699, LY3045697, baxdrostat) vs. Placebo or active controls (e.g., eplerenone, spironolactone) was evaluated on Reduction in systolic and diastolic blood pressure, and reduction of aldosterone or cortisol. Aldosterone synthase inhibitors, particularly baxdrostat, effectively reduce systolic and diastolic blood pressure in patients with essential and resistant hypertension by selectively decreasing aldosterone levels.
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