M. Hausberg et al., ACE inhibitor versus beta-blocker for the treatment of hypertension in renal allograft recipients, HYPERTENSIO, 33(3), 1999, pp. 862-868
Citations number
41
Categorie Soggetti
Cardiovascular & Respiratory Systems","Cardiovascular & Hematology Research
Angiotensin-converting enzyme (ACE) inhibitors have been shown to slow the
progression of chronic renal failure. However, the value of ACE inhibitors
for the treatment of hypertension in renal allograft recipients has not bee
n established. ACE inhibitors dilate the efferent glomerular arteriole, an
effect that may aggravate the decrease in glomerular filtration rate result
ing from cyclosporine-induced vasoconstriction at the afferent glomerular a
rteriole. Therefore, the goal of this double-blind, randomized study was to
compare the antihypertensive and renal effects of the ACE inhibitor quinap
ril with those of the beta-blocker atenolol in renal allograft recipients i
n whom hypertension developed 6 to 12 weeks after transplantation. All pati
ents received cyclosporine as an immunosuppressant and had stable graft fun
ction (serum creatinine concentration, <220 mu mol/L) at entry into the stu
dy. Twenty-nine patients who received quinapril (daily dose titrated betwee
n 2.5 and 20 mg) and 30 patients who received atenolol (daily dose titrated
between 12.5 and 100 mg) completed the 24-month study. The two groups did
not differ in age, sex ratio, height, and weight before entry into the stud
y. Quinapril decreased diastolic blood pressure from 96+/-1 to 84+/-1 mm Hg
(average throughout treatment period), and atenolol decreased diastolic bl
ood pressure from 96+/-1 to 83+/-1 mm Hg. The serum creatinine concentratio
n did not change significantly in either group after 24 months (129+/-8 mu
mol/L at entry and 148+/-19 mu mol/L after 24 months in the quinapril group
and 131+/-6 mu mol/L at entry and 152+/-15 mu mol/L after 24 months in the
atenolol group; P=NS for both groups). After 23 months, the change in urin
ary albumin excretion from baseline was -10+/-15 mg/d in the quinapril grou
p and 52+/-32 mg/d in the atenolol group (P = 0.03). These results show tha
t quinapril and atenolol are effective antihypertensive drugs when used aft
er renal transplantation. Moreover, compared with atenolol, quinapril has n
o adverse effects on graft function. The relative reduction in albuminuria
observed with quinapril as compared with atenolol could indicate a benefici
al effect of quinapril on long-term graft function.