Awosika Ayoola, Khan Anosh, Adabanya Uzochukwu, Omole Adekunle E, Millis Richard M
College of Medicine, University of Illinois Chicago, Chicago, USA.
Internal Medicine, Spartan Health Sciences University School of Medicine, Vieux Fort, LCA.
Cureus. 2023 Mar 15;15(3):e36184. doi: 10.7759/cureus.36184. eCollection 2023 Mar.
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.
系统性高血压(HTN)是心血管疾病的标志,也是心力衰竭的先兆。这些关联是在对原发性高血压进行数十年研究后确立的。对于被诊断为HTN的患者,其治疗方法包括使用α或β肾上腺素能受体阻滞剂、钙通道阻滞剂、血管紧张素转换酶抑制剂、噻嗪类药物或被称为抗盐皮质激素的醛固酮受体阻滞剂,无论是否采用低钠盐饮食,往往都无法充分控制血压以预防发病和死亡。低钠盐饮食在控制HTN方面成效有限,因为低钠摄入与肾素-血管紧张素-醛固酮系统上调有关。因此,醛固酮分泌、钠和水潴留上调,作为一种代偿机制,进而使血压回升至压力感受器重置值所决定的HTN范围,尤其是在顽固性HTN中。一类名为醛固酮合酶抑制剂的新型药物的出现,可能有效规避了这些HTN血压控制方面的障碍,以巴多司他为代表。巴多司他作为醛固酮合酶抑制剂的作用机制表明了钠与血压调节之间存在着紧密联系。从理论上讲,将低钠盐饮食与这种醛固酮合成抑制剂的作用相结合,应能减轻肾素-血管紧张素-醛固酮系统上调的不良影响。醛固酮合成抑制还应能降低与HTN相关的氧化应激和内皮功能障碍,促使更多内皮一氧化氮合成、释放并引起血管舒张。据我们所知,这是第一篇系统综述,总结了与使用新型药物(醛固酮合酶抑制剂)治疗HTN和心血管疾病相关的循证文章。使当前关于巴多司他和其他醛固酮合酶抑制剂的相关信息数据库易于获取,无疑将有助于医生和其他医学从业者在决定是否使用醛固酮合酶抑制剂治疗患者时做出决策。