Left Ventricular Hypertrophy and Antihypertensive Therapy

Drugs ◽  
1988 ◽  
Vol 35 (Supplement 5) ◽  
pp. 27-33 ◽  
Author(s):  
Franz H. Messerli ◽  
Shmuel Oren ◽  
Ehud Grossman
2000 ◽  
Vol 41 (3) ◽  
pp. 339-348
Author(s):  
Sumino Hiroyuki ◽  
Nakamura Tetsuya ◽  
Kanda Tsugiyasu ◽  
Sakamaki Tetsuo ◽  
Sato Kunio ◽  
...  

2000 ◽  
Vol 18 ◽  
pp. S64
Author(s):  
A. Szyszka ◽  
A. Cieśliński ◽  
R. Ochotny ◽  
M. Waśniewski ◽  
E. Straburzyńska-Migaj ◽  
...  

2019 ◽  
Vol 8 (10) ◽  
pp. 1671 ◽  
Author(s):  
Beata Krasińska ◽  
Szczepan Cofta ◽  
Ludwina Szczepaniak-Chicheł ◽  
Piotr Rzymski ◽  
Tomasz Trafas ◽  
...  

The obstructive sleep apnea (OSA) is highly associated with various significant cardiovascular outcomes such as resistant hypertension (RAH). Despite this, as of now the relationship between high night-time blood pressure (BP) and left ventricular hypertrophy (LVH) in patients with OSA and RAH is not fully understood. The aim of this study was to assess the influence of the addition of eplerenone to a standard antihypertensive therapy on parameters of 24-h ambulatory blood pressure measurement (ABPM) as well as on the results of echocardiography and polysomnography in patients with OSA and RAH. The patients were randomly assigned to one of the two study groups: the treatment group, receiving 50 mg/d eplerenone orally for 6 months (n = 51) and the control group, remaining on their standard antihypertensive therapy (n = 51). After that period, a significant reduction in the night-time BP parameters in the treatment group including an increased night blood pressure fall from 4.6 to 8.9% was noted. Additionally, the number of non-dipper patients was reduced by 45.1%. The treatment group also revealed a decrease in left ventricular hypertrophy and in the apnea–hypopnea index (AHI) with a positive correlation being observed between these two parameters. This study is the first to report the improvement of the circadian BP profile and the improvement of the left ventricle geometry in patients with OSA and RAH following the addition of selective mineralocorticoid receptor antagonists to antihypertensive therapy.


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