C. Alli et al., ALBUMINURIA AND TRANSFERRINURIA IN ESSENTIAL-HYPERTENSION - EFFECTS OF ANTIHYPERTENSIVE THERAPY, American journal of hypertension, 9(11), 1996, pp. 1068-1076
The objectives of this study were to evaluate the effects of an ACE in
hibitor (fosinopril) and a calcium antagonist (amlodipine) on the urin
ary albumin and transferrin excretion and their relationship to the bl
ood pressure in essential hypertension. Twenty-four never-treated pati
ents (mean age, 46.4 +/- 8.9 years) with a diastolic blood pressure be
tween 90 and 114 mm Hg and normal renal function, randomly received am
lodipine or fosinopril and, if the diastolic blood pressure was not no
rmalized, doxazosin was added to the therapy. Twenty-four-hour ambulat
ory blood pressure monitoring and 24-h urine collection for albumin an
d transferrin measurements were performed before and after 3 and 6 mon
ths of therapy. Diastolic blood pressure was normalized in 23 patients
(96%). Before treatment, microalbuminuria was present in 50% of patie
nts. In the amlodipine and fosinopril group, antihypertensive therapy
significantly decreased blood pressure and, only in the fosinopril gro
up, albuminuria, Transferrinuria did not change significantly in both
groups. Fosinopril lowered albuminuria in all patients, whereas amlodi
pine only in half of patients, Albuminuria, but not transferrinuria, w
as significantly correlated to the ambulatory blood pressure. This cor
relation was more pronounced for systolic than for diastolic pressure.
In essential hypertensive patients with normal renal function, a high
prevalence of microalbuminuria can be observed. Albuminuria appears t
o correlate with ambulatory blood pressure, particularly with systolic
pressure. Intrarenal hemodynamic changes seem to play a more importan
t role than systemic blood pressure decrease in the reduction of album
inuria. Transferrinuria does not seem a useful marker to follow-up non
diabetic hypertensive patients with early signs of glomerular dysfunct
ion.