Randomised controlled trial of dual blockade of renin-angiotensin system in patients with hypertension, microalbuminuria, and non-insulin dependent diabetes: the candesartan and Lisinopril microalbuminuria (CALM) study
Ce. Mogensen et al., Randomised controlled trial of dual blockade of renin-angiotensin system in patients with hypertension, microalbuminuria, and non-insulin dependent diabetes: the candesartan and Lisinopril microalbuminuria (CALM) study, BR MED J, 321(7274), 2000, pp. 1440-1444
Citations number
30
Categorie Soggetti
General & Internal Medicine","Medical Research General Topics
Objectives To assess and compare the effects of candesartan or lisinopril,
or both, on blood pressure and urinary albumin excretion in patients with m
icroalbuminuria, hypertension, and type 2 diabetes.
Design Prospective, randomised, parallel group, double blind study with fou
r week placebo run in period and 12 weeks' monotherapy with candesartan or
lisinopril followed by 12 weeks' monotherapy or combination treatment
Setting Tertiary hospitals and primary care centres in four countries (37 c
entres).
Participants 199 patients aged 30-75 years.
Interventions Candesartan 16 mp; once daily, lisinopril 20 mg once daily.
Main outcome measures Blood pressure and urinary albumin:creatinine ratio.
Results At 12 creeks mean (95% confidence interval) reductions in diastolic
blood pressure were 9.5 mm Hg (7.7 mm Hg to 11.2 mm Hg, P < 0.002) and 9.7
mm Hg (7.9 mm Hg to 115 mm Hg, P < 0.001), respectively, and in urinary al
bumin:creatinine ratio were 30% (15% to 42%, P < 0.001) and 46% (35% to 56%
, P < 0.001) for candesartan and lisinopril, respectively. At 24 weeks the
mean reduction in diastolic blood pressure with combination treatment (16.3
mm Hg, 13.6 mm Hg to 18.9 mm Hg, P < 0.001) was significantly greater than
that with candesartan (10.4 mm Hg, 7.7 mm Hg to 13.1 mm Hg, P < 0.001) or
lisinopril (mean 10.7 mm Hg. 8.0 nun Hg to 13.5 mm Hg, P < 0.001). Furtherm
ore, the reduction in urinary albumin:creatinine ratio with combination tre
atment (50%, 36% to 61%, P<0.001) was greater than with candesartan (24%, 0
% to 43%, P = 0.05) and lisinopril (39%, 20% to 54%, P < 0.001). All treatm
ents were generally well tolerated.
Conclusion Candesartan 16 mg once daily is as effective as lisinopril 20 mg
once daily in reducing blood pressure and microalbuminuria in hypertensive
patients with type 2 diabetes. Combination treatment is well tolerated and
more effective in reducing blood pressure.