TY - JOUR
T1 - Association between aldosterone induced by antihypertensive medication and arterial stiffness reduction
T2 - The J-CORE study
AU - Matsui, Yoshio
AU - Eguchi, Kazuo
AU - O'Rourke, Michael F.
AU - Ishikawa, Joji
AU - Shimada, Kazuyuki
AU - Kario, Kazuomi
N1 - Funding Information:
The J-CORE study was supported by a grant from Jichi Medical University School of Medicine .
PY - 2011/3
Y1 - 2011/3
N2 - Objective: Excess aldosterone has a detrimental effect on large artery stiffness. We aimed to investigate the association of the change in plasma aldosterone concentration (PAC) by antihypertensive medication with the change in aortic pulse wave velocity (aPWV). Methods: We conducted a prospective, randomized, open-label, blinded end-point study in 207 hypertensive patients. Patients received olmesartan monotherapy for 12 weeks, followed by add-on use of hydrochlorothiazide (HCTZ; n= 104) or azelnidipine (n= 103) for 24 weeks after randomization. The aPWV, which was determined by measuring the carotid to femoral PWV, and laboratory data were assessed at baseline and 24 weeks later. Results: PAC in the HCTZ group increased more than that in the azelnidipine group, while aPWV and mean arterial pressure in the azelnidipine group decreased more than those in the HCTZ group. In univariable analyses, the change in PAC was significantly and positively correlated with the change in aPWV in the total population (r= 0.26, P< 0.001) and the HCTZ group (r= 0.28, P= 0.004), but not in the azelnidipine group (r= 0.17, P= 0.09). In multivariable analyses, a positive association of the change in PAC with the change in aPWV was observed in the total population (standardized regression coefficient β= 0.18, P< 0.001) and the HCTZ group (β= 0.23, P= 0.004), independently of the changes in covariates, but not in the azelnidipine group (β= 0.13, P= 0.06). Conclusion: The change in PAC was significantly and positively associated with the change in aPWV in patients treated with HCTZ. These findings may partly explain why thiazide diuretics have little effect on large artery stiffness.
AB - Objective: Excess aldosterone has a detrimental effect on large artery stiffness. We aimed to investigate the association of the change in plasma aldosterone concentration (PAC) by antihypertensive medication with the change in aortic pulse wave velocity (aPWV). Methods: We conducted a prospective, randomized, open-label, blinded end-point study in 207 hypertensive patients. Patients received olmesartan monotherapy for 12 weeks, followed by add-on use of hydrochlorothiazide (HCTZ; n= 104) or azelnidipine (n= 103) for 24 weeks after randomization. The aPWV, which was determined by measuring the carotid to femoral PWV, and laboratory data were assessed at baseline and 24 weeks later. Results: PAC in the HCTZ group increased more than that in the azelnidipine group, while aPWV and mean arterial pressure in the azelnidipine group decreased more than those in the HCTZ group. In univariable analyses, the change in PAC was significantly and positively correlated with the change in aPWV in the total population (r= 0.26, P< 0.001) and the HCTZ group (r= 0.28, P= 0.004), but not in the azelnidipine group (r= 0.17, P= 0.09). In multivariable analyses, a positive association of the change in PAC with the change in aPWV was observed in the total population (standardized regression coefficient β= 0.18, P< 0.001) and the HCTZ group (β= 0.23, P= 0.004), independently of the changes in covariates, but not in the azelnidipine group (β= 0.13, P= 0.06). Conclusion: The change in PAC was significantly and positively associated with the change in aPWV in patients treated with HCTZ. These findings may partly explain why thiazide diuretics have little effect on large artery stiffness.
KW - Aldosterone
KW - Aortic pulse wave velocity
KW - Calcium channel blocker
KW - Mean arterial pressure
KW - Thiazide diuretic
UR - https://www.scopus.com/pages/publications/79952102598
U2 - 10.1016/j.atherosclerosis.2010.12.022
DO - 10.1016/j.atherosclerosis.2010.12.022
M3 - Article
C2 - 21241987
AN - SCOPUS:79952102598
SN - 0021-9150
VL - 215
SP - 184
EP - 188
JO - Atherosclerosis
JF - Atherosclerosis
IS - 1
ER -