Rh. Fagard et al., OPPOSITE ASSOCIATIONS OF CIRCULATING ALDOSTERONE AND ATRIAL-NATRIURETIC-PEPTIDE WITH LEFT-VENTRICULAR DIASTOLIC FUNCTION IN ESSENTIAL-HYPERTENSION, Journal of human hypertension, 12(3), 1998, pp. 195-202
It has been shown in animal experiments that angiotensin II and aldost
erone have mitogenic effects on the cardiovascular system, whereas atr
ial natriuretic peptide has antimitogenic properties. The aim of the p
resent study was to relate plasma renin activity, angiotensin II, aldo
sterone and atrial natriuretic peptide to left ventricular structure a
nd function, assessed by use of imaging echocardiography and transmitr
al Doppler velocimetry in 73 patients with essential hypertension, Wor
ld Health Organization stages I-II, aged 43 +/- 10(s.d.) years. Left v
entricular mass, wall thickness and internal diameter were not indepen
dently related to the biochemical variables, except for a weak and pos
itive association of wall thickness with plasma aldosterone (P = 0.06)
. However, left ventricular early inflow peak velocity and deceleratio
n were independently and inversely related to age (P < 0.001) and to p
lasma aldosterone (P < 0.01), and positively to plasma atrial natriure
tic peptide (P < 0.05). Peak flow velocity during atrial contraction w
as positively related to plasma atrial natriuretic peptide both before
(P < 0.001) and after (P < 0.05) controlling for significant covariat
es (age, sex and blood pressure). We conclude that circulating renin,
angiotensin II, aldosterone and atrial natriuretic peptide are not ind
ependently related to left ventricular mass in essential hypertension.
The inverse association of plasma aldosterone with indices of diastol
ic function is compatible with a stimulating effect of aldosterone on
myocardial fibrosis, which is opposed by atrial natriuretic peptide. T
he apparently conflicting positive association of this peptide with at
rial peak velocity is most likely due to stimulation of its secretion
by atrial involvement.