Apparent treatment-resistant hypertension and chronic kidney disease: another cardiovascular-renal syndrome?


Autoria(s): Vemulapalli, S; Tyson, CC; Svetkey, LP
Data(s)

01/11/2014

Formato

489 - 499

Identificador

http://www.ncbi.nlm.nih.gov/pubmed/25443574

S1548-5595(14)00144-X

Adv Chronic Kidney Dis, 2014, 21 (6), pp. 489 - 499

http://hdl.handle.net/10161/10737

1548-5609

Relação

Adv Chronic Kidney Dis

10.1053/j.ackd.2014.08.006

Palavras-Chave #Aldosterone #Cardiovascular outcomes #Chronic kidney disease #Diuretic #Resistant hypertension #Aldosterone #Antihypertensive Agents #Blood Volume #Cardio-Renal Syndrome #Coronary Vasospasm #Diuretics #Drug Resistance #Electric Stimulation Therapy #Humans #Hypertension #Pressoreceptors #Receptors, Mineralocorticoid #Renal Insufficiency, Chronic #Renin-Angiotensin System #Sympathectomy #Sympathetic Nervous System
Tipo

Journal Article

Cobertura

United States

Resumo

To identify patients at increased risk of cardiovascular (CV) outcomes, apparent treatment-resistant hypertension (aTRH) is defined as having a blood pressure above goal despite the use of 3 or more antihypertensive therapies of different classes at maximally tolerated doses, ideally including a diuretic. Recent epidemiologic studies in selected populations estimated the prevalence of aTRH as 10% to 15% among patients with hypertension and that aTRH is associated with elevated risk of CV and renal outcomes. Additionally, aTRH and CKD are associated. Although the pathogenesis of aTRH is multifactorial, the kidney is believed to play a significant role. Increased volume expansion, aldosterone concentration, mineralocorticoid receptor activity, arterial stiffness, and sympathetic nervous system activity are central to the pathogenesis of aTRH and are targets of therapies. Although diuretics form the basis of therapy in aTRH, pathophysiologic and clinical data suggest an important role for aldosterone antagonism. Interventional techniques, such as renal denervation and carotid baroreceptor activation, modulate the sympathetic nervous system and are currently in phase III trials for the treatment of aTRH. These technologies are as yet unproven and have not been investigated in relationship to CV outcomes or in patients with CKD.

Idioma(s)

ENG