Background The multicenter double-blind, randomized BergamoNephrologic Diabetes Complications Trial (BENEDICT) was designedto assess whether angiotensin-convertingenzyme inhibitorsand non-dihydropyridine calcium-channel blockers, alone or incombination, prevent microalbuminuria in subjects with hypertension,type 2 diabetes mellitus, and normal urinary albumin excretion.
Methods We studied 1204 subjects, who were randomly assignedto receive at least three years of treatment with trandolapril(at a dose of 2 mg per day) plus verapamil (sustained-releaseformulation, 180 mg per day), trandolapril alone (2 mg per day),verapamil alone (sustained-release formulation, 240 mg per day),or placebo. The target blood pressure was 120/80 mm Hg. Theprimary end point was the development of persistent microalbuminuria(overnight albumin excretion, 20 µg per minute at twoconsecutive visits).
Results The primary outcome was reached in 5.7 percent of thesubjects receiving trandolapril plus verapamil, 6.0 percentof the subjects receiving trandolapril, 11.9 percent of thesubjects receiving verapamil, and 10.0 percent of control subjectsreceiving placebo. The estimated acceleration factor (whichquantifies the effect of one treatment relative to another inaccelerating or slowing disease progression) adjusted for predefinedbaseline characteristics was 0.39 for the comparison betweenverapamil plus trandolapril and placebo (P=0.01), 0.47 for thecomparison between trandolapril and placebo (P=0.01), and 0.83for the comparison between verapamil and placebo (P=0.54). Trandolaprilplus verapamil and trandolapril alone delayed the onset of microalbuminuriaby factors of 2.6 and 2.1, respectively. Serious adverse eventswere similar in all treatment groups.
Conclusions In subjects with type 2 diabetes and hypertensionbut with normoalbuminuria, the use of trandolapril plus verapamiland trandolapril alone decreased the incidence of microalbuminuriato a similar extent. The effect of verapamil alone was similarto that of placebo.
Source Information
From the Mario Negri Institute for Pharmacological Research, Clinical Research Center for Rare Diseases, Aldo e Cele Daccò, Villa Camozzi, Ranica, Bergamo (P.R., A.F., A.P.I., S.B., I.P.I., V.B., N.R., G.G., F.A., M.G., B.E.-I., F.G., A.P., G.R.); the Unit of Nephrology, Azienda Ospedaliera, Ospedali Riuniti, Bergamo (P.R., G.R.); the Unit of Diabetology of the Treviglio Hospital, Treviglio (A.B.); and the Unit of Diabetology of the Bergamo Hospital, Bergamo (R.T., A.R.D.) all in Italy.
Address reprint requests to Dr. Ruggenenti at the Mario Negri Institute for Pharmacological Research, Via Gavazzeni, 11, 24125 Bergamo, Italy, or at manuelap{at}marionegri.it.
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