Effect of 3 Years of Antihypertensive Therapy on Renal Structure in Type 1 Diabetic Patients With Albuminuria

The European Study for the Prevention of Renal Disease in Type 1 Diabetes (ESPRIT)

  1. The European Study for the Prevention of Renal Disease in Type 1 Diabetes ESPRIT Study Group

    Abstract

    In the treatment of diabetic nephropathy, ACE inhibitor therapy reduces albumin excretion and slows the rate of decline in glomerular filtration rate (GFR). Our study was designed to investigate whether these effects lay in amelioration of the underlying glomerular structural abnormalities. A total of 54 type 1 diabetic patients with albuminuria and blood pressure (BP) <150/90 mmHg were randomized to receive 10 mg enalapril once daily, 10 mg nifedipine retard twice daily, or placebo in a multicenter double-blind study of 3 years’ duration. Renal biopsy was performed at baseline and follow-up, and tissue was analyzed by standard morphometric methods. BP, GFR, albumin excretion rate (AER), and HbA1c were measured every 6 months. Enalapril lowered AER after 6 months by 26% (P < 0.05); however, this reduction was not sustained at 3 years. There was no significant effect of nifedipine or placebo on AER. GFR decreased by a similar average rate of 4.1 ml · min–1 · year–1 (95% CI 2.6–5.6) in all three groups. BP and HbA1c were unchanged throughout the study in all groups. At baseline, nearly all biopsies showed classic appearances of diabetic glomerulopathy. There was no detectable effect of enalapril compared with either nifedipine or placebo on renal structure over 3 years. However, we found that patients with increased AER have established glomerulopathy and a progressive average decline in GFR of 4.1 ml · min–1 · year–1 in the absence of overt hypertension, and baseline AER appeared predictive of subsequent mesangial volume fraction (r2 = 0.20, P = 0.0018). In this small cohort of nonhypertensive patients studied for 3 years, disease evolution appears unaffected by treatment with either enalapril or nifedipine.

    Footnotes

    • Address correspondence and reprint requests to Dr. Laura A. Baines, Audrey Collins Teaching Centre, South Cleveland Hospital, Marton Road, Middlesbrough TS4 3BW, U.K. E-mail: l.a.baines{at}ncl.ac.uk.

      Received for publication 19 January 2000 and accepted in revised form 11 December 2000.

      †A complete list of centers and investigators is listed in the appendix.

      Helen Tate has received consulting fees from Merck, Sharp, and Dohme. R. W. Bilous and L. A. Baines have received grant and research funds from Merck, Sharp, and Dohme.

    « Previous | Next Article »Table of Contents