Laboratory of Translational Hypertension and Vascular Research, Department of General Surgery, Wake Forest School of Medicine, Medical Center Blvd, Atrium Health Wake Forest Baptist, Winston Salem, NC, 27157, USA.
Department of Anesthesiology, Wake Forest School of Medicine, Medical Center Blvd, Atrium Health Wake Forest Baptist, Winston Salem, NC, 27157, USA.
Curr Hypertens Rep. 2022 Dec;24(12):709-721. doi: 10.1007/s11906-022-01229-x. Epub 2022 Oct 22.
To address contemporary hypertension challenges, a critical reexamination of therapeutic accomplishments using angiotensin converting enzyme inhibitors and angiotensin II receptor blockers, and a greater appreciation of evidence-based shortcomings from randomized clinical trials are fundamental in accelerating future progress.
Medications targeting angiotensin II mechanism of action are essential for managing primary hypertension, type 2 diabetes, heart failure, and chronic kidney disease. While the ability of angiotensin converting enzyme inhibitors and angiotensin II receptor blockers to control blood pressure is undisputed, practitioners, hypertension specialists, and researchers hold low awareness of these drugs' limitations in preventing or reducing the risk of cardiovascular events. Biases in interpreting gained knowledge from data obtained in randomized clinical trials include a pervasive emphasis on using relative risk reduction over absolute risk reduction. Furthermore, recommendations for clinical practice in international hypertension guidelines fail to address the significance of a residual risk several orders of magnitude greater than the benefits. We analyze the limitations of the clinical trials that have led to current recommended treatment guidelines. We define and quantify the magnitude of the residual risk in published hypertension trials and explore how activation of alternate compensatory bioprocessing components within the renin angiotensin system bypass the ability of angiotensin converting enzyme inhibitors and angiotensin II receptor blockers to achieve a significant reduction in total and cardiovascular deaths. We complete this presentation by outlining the current incipient but promising potential of immunotherapy to block angiotensin II pathology alone or possibly in combination with other antihypertensive drugs. A full appreciation of the magnitude of the residual risk associated with current renin angiotensin system-based therapies constitutes a vital underpinning for seeking new molecular approaches to halt or even reverse the cardiovascular complications of primary hypertension and encourage investigating a new generation of ACE inhibitors and ARBs with increased capacity to reach the intracellular compartments at which Ang II can be generated.
为应对当代高血压挑战,需要重新审视血管紧张素转换酶抑制剂和血管紧张素 II 受体阻滞剂的治疗效果,并更加重视随机临床试验的循证不足,这对于加速未来进展至关重要。
针对血管紧张素 II 作用机制的药物对于原发性高血压、2 型糖尿病、心力衰竭和慢性肾脏病的治疗至关重要。血管紧张素转换酶抑制剂和血管紧张素 II 受体阻滞剂控制血压的能力无可争议,但临床医生、高血压专家和研究人员对这些药物在预防或降低心血管事件风险方面的局限性认识不足。从随机临床试验中获得的知识的解释存在偏见,包括普遍强调用相对风险降低而不是绝对风险降低。此外,国际高血压指南中的临床实践建议未能解决比获益大几个数量级的残余风险的重要性。我们分析了导致当前推荐治疗指南的临床试验的局限性。我们定义并量化了已发表的高血压试验中残余风险的幅度,并探讨了肾素血管紧张素系统内替代补偿生物处理成分的激活如何绕过血管紧张素转换酶抑制剂和血管紧张素 II 受体阻滞剂实现总死亡率和心血管死亡率显著降低的能力。我们通过概述免疫疗法单独或可能与其他降压药物联合阻断血管紧张素 II 病理的当前初现但有前途的潜力来完成本报告。充分认识与当前基于肾素血管紧张素系统的治疗相关的残余风险的幅度,对于寻求阻止甚至逆转原发性高血压心血管并发症的新分子方法至关重要,并鼓励研究新一代 ACE 抑制剂和 ARB,以增加到达其中可以产生 Ang II 的细胞内隔室的能力。