Department of Medicine, Division of General Internal Medicine, Hypertension Section, Southern Illinois University, Southern Illinois University School of Medicine, 801 North Rutledge Street, Carbondale, IL, 62702, USA.
Department of Medicine and the Center for Clinical Research, Southern Illinois University, Carbondale, IL, USA.
Curr Hypertens Rep. 2024 May;26(5):183-199. doi: 10.1007/s11906-023-01282-0. Epub 2024 Feb 16.
PURPOSE OF REVIEW: To define resistant hypertension (RHT), review its pathophysiology and disease burden, identify barriers to effective hypertension management, and to highlight emerging treatment options. RECENT FINDINGS: RHT is defined as uncontrolled blood pressure (BP) ≥ 130/80 mm Hg despite concurrent prescription of ≥ 3 or ≥ 4 antihypertensive drugs in different classes or controlled BP despite prescription of ≥ to 4 drugs, at maximally tolerated doses, including a diuretic. BP is regulated by a complex interplay between the renin-angiotensin-aldosterone system, the sympathetic nervous system, the endothelin system, natriuretic peptides, the arterial vasculature, and the immune system; disruption of any of these can increase BP. RHT is disproportionately manifest in African Americans, older patients, and those with diabetes and/or chronic kidney disease (CKD). Amongst drug-treated hypertensives, only one-quarter have been treated intensively enough (prescribed > 2 drugs) to be considered for this diagnosis. New treatment strategies aimed at novel therapeutic targets include inhibition of sodium-glucose cotransporter 2, aminopeptidase A, aldosterone synthesis, phosphodiesterase 5, xanthine oxidase, and dopamine beta-hydroxylase, as well as soluble guanylate cyclase stimulation, nonsteroidal mineralocorticoid receptor antagonism, and dual endothelin receptor antagonism. The burden of RHT remains high. Better use of currently approved therapies and integrating emerging therapies are welcome additions to the therapeutic armamentarium for addressing needs in high-risk aTRH patients.
目的综述:定义耐药性高血压(RHT),综述其病理生理学和疾病负担,确定有效高血压管理的障碍,并强调新兴的治疗选择。
最近的发现:RHT 被定义为尽管同时处方≥3 种或≥4 种不同类别的抗高血压药物,或尽管处方最大耐受剂量的≥4 种药物(包括利尿剂)控制血压,但血压仍不受控制(BP)≥130/80mmHg。BP 受肾素-血管紧张素-醛固酮系统、交感神经系统、内皮素系统、利钠肽、动脉血管和免疫系统之间复杂相互作用的调节;这些系统中的任何一个中断都可能增加 BP。RHT 在非裔美国人、老年患者以及患有糖尿病和/或慢性肾脏病(CKD)的患者中不成比例地表现出来。在接受药物治疗的高血压患者中,只有四分之一接受了足够强化的治疗(处方>2 种药物),以考虑进行这种诊断。旨在针对新治疗靶点的新治疗策略包括抑制钠-葡萄糖共转运蛋白 2、氨基肽酶 A、醛固酮合成、磷酸二酯酶 5、黄嘌呤氧化酶和多巴胺β-羟化酶,以及可溶性鸟苷酸环化酶刺激、非甾体类盐皮质激素受体拮抗剂和双重内皮素受体拮抗剂。RHT 的负担仍然很高。更好地利用目前批准的治疗方法和整合新兴治疗方法是为解决高危 aTRH 患者的需求而增加治疗手段的可喜补充。
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