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Clinical Trial
. 2000 Dec 9;321(7274):1440-4.
doi: 10.1136/bmj.321.7274.1440.

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

Affiliations
Clinical Trial

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

C E Mogensen et al. BMJ. .

Abstract

Objectives: To assess and compare the effects of candesartan or lisinopril, or both, on blood pressure and urinary albumin excretion in patients with microalbuminuria, hypertension, and type 2 diabetes.

Design: Prospective, randomised, parallel group, double blind study with four 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 centres).

Participants: 199 patients aged 30-75 years.

Interventions: Candesartan 16 mg once daily, lisinopril 20 mg once daily.

Main outcome measures: Blood pressure and urinary albumin:creatinine ratio.

Results: At 12 weeks mean (95% confidence interval) reductions in diastolic blood pressure were 9.5 mm Hg (7.7 mm Hg to 11.2 mm Hg, P<0.001) and 9.7 mm Hg (7.9 mm Hg to 11.5 mm Hg, P<0.001), respectively, and in urinary albumin: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 mm Hg to 13.5 mm Hg, P<0.001). Furthermore, the reduction in urinary albumin:creatinine ratio with combination treatment (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 treatments 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.

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Figures

Figure 1
Figure 1
Distribution of participants in study. Doses were: candesartan 16 mg once daily, lisinopril 20 mg once daily, or their combination
Figure 2
Figure 2
Mean (SE) seated systolic and diastolic blood pressure in patients with type 2 diabetes mellitus, hypertension, and microalbuminuria before and during treatment with candesartan 16 mg once daily (n=49), lisinopril 20 mg once daily (n=46), or combination of candesartan and lisinopril (n=49). Combination group received monotherapy with either candesartan or lisinopril for first 12 weeks

Comment in

References

    1. Cooper ME. Pathogenesis, prevention and treatment of diabetic nephropathy. Lancet. 1998;352:213–219. - PubMed
    1. Mathiesen ER, Hommel E, Hansen HP, Smidt UH, Parving HH. Randomised controlled trial of long term efficacy of captopril on preservation of kidney function in normotensive patients with insulin dependent diabetes and microalbuminuria. BMJ. 1999;319:24–25. - PMC - PubMed
    1. Mogensen CE, Keane WF, Bennett PH, Jerums G, Parving HH, Passa P, et al. Prevention of diabetic renal disease with special reference to microalbuminuria. Lancet. 1995;346:1080–1084. - PubMed
    1. Azizi M, Chatellier G, Guyene TT, Murietageoffroy D, Menard J. Additive effects of combined angiotensin-converting enzyme inhibition and angiotensin II antagonism on blood pressure and renin release in sodium-depleted normotensives. Circulation. 1995;92:825–834. - PubMed
    1. Hollenberg NK, Fisher NDL, Price DA. Pathways for angiotensin II generation in intact human tissue—evidence from comparative pharmacological interruption of the renin system. Hypertension. 1998;32:387–392. - PubMed