Dual Blockade of the Renin-Angiotensin System in Diabetic Nephropathy

A randomized double-blind crossover study

  1. Kasper Rossing, MD,
  2. Per K. Christensen, MD,
  3. Berit R. Jensen and
  4. Hans-Henrik Parving, Prof., MD, DMSC
  1. Steno Diabetes Center, Gentofte, Denmark

    Abstract

    OBJECTIVE—Many patients with diabetic nephropathy (DN) have levels of albuminuria >1 g/day and blood pressure >135/85 mmHg, despite antihypertensive combination therapy, including recommended doses of ACE inhibitors, e.g., lisinopril/enalapril at 20 mg daily. We tested the concept that such patients might benefit from dual blockade of the renin-angiotensin system (RAS).

    RESEARCH DESIGN AND METHODS—We performed a randomized double-blind crossover study of 2 months treatment with candesartan cilexetil 8 mg once daily and placebo in addition to previous antihypertensive treatment. We included 18 type 2 diabetic patients with DN fulfilling the above-mentioned criteria. All received recommended doses of ACE inhibitor and, in addition, 15 patients received diuretics, 11 received a calcium channel antagonist, and 3 received a β-blocker. At the end of each treatment period, we measured the glomerular filtration rate (GFR), 24-h blood pressure, albuminuria, and IgGuria .

    RESULTS—The addition of candesartan to usual antihypertensive therapy induced a mean (95% CI) reduction in albuminuria of 25% (2–58), P = 0.036 (geometric mean [95% CI] from 1,764 mg/24 h [1,225–2,540] to 1,334 mg/24 h [890–1,998]). It also produced a mean reduction of 35% (9–53) in the fractional clearance of albumin (P = 0.016), a reduction of 32% (1–54) in fractional clearance of IgG (P = 0.046), a reduction in 24-h systolic blood pressure of 10 mmHg (2–18) (P = 0.019) (mean ± ± SE) from 148 ± 3 to 138 ± 5 mmHg, and a mean reduction in GFR of 5 ml · min−1 · 1.73 m−2 (0.1–9) (P = 0.045).

    CONCLUSIONS—Dual blockade of the RAS reduces albuminuria and blood pressure in type 2 diabetic patients with DN responding insufficiently to previous antihypertensive therapy, including ACE inhibitors in recommended doses.

    Footnotes

    • Address correspondence and reprint requests to Kasper Rossing, Steno Diabetes Center, Niels Steensens Vej 2, Dk-2820 Gentofte, Denmark. E-mail: krossing{at}dadlnet.dk.

      Received for publication 20 June 2001 and accepted in revised form 21 September 2001.

      H.-H.P. has received honoraria or consulting fees from Merck, AstraZeneca, BMS, Sanofi-Synthelabo, and Pfizer, and he has received grant/research support from Merck and Sanofi-Synthelabo.

      A table elsewhere in this issue shows conventional and Systéme International (SI) units and conversion factors for many substances.

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