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Nephrol Dial Transplant (1996) 11: 673-678
© 1996 European Renal Association-European Dialysis and Transplant Association


research-article

Angiotensin converting enzyme inhibition and chronic cyclosporine-induced renal dysfunction in type 1 diabetes

Thierry P. Hannedouche, Svetlozar Natov, Christian Boitard, Bernard Lacour and Jean-Pierre Grünfeld

Département de Néphrologie, Hôpital Necker Paris, France

Correspondence and offprint requests to: Correspondence and offprint requests to: Prof. T. Hannedouche, Département de Néphrologie, Hôpitaux Universitaires de Strasbourg, BP 426, 67091 Strasbourg, France

AIM.: This study was designed to evaluate whether the angiotensin converting enzyme inhibitor enalapril could prevent cyclosporine-induced renal dysfunction in diabetic patients treated with CsA in monotherapy.

DESIGN.: Twenty-four recent onset insulin-dependent diabetic patients without prior renal involvement were randomized to receive a 3 month course of either cyclosporine (CsA) alone (7.5 mg/kg. b.i.d. in olive oil) or CsA$enalapril (20 mg p.o. oad.).

END POINTS.: were mean arterial pressure, plasma creatinine, GFR, renal plasma flow, renal vascular resistance, sodium and lithium clearances measured before and after 3 months of treatment.

RESULTS.: Baseline values were identical in both groups except for mean arterial pressure which was slightly higher in the subjects subsequently receiving CsA$enalapril. Three month treatment with CsA increased significantly mean arterial pressure and renal vascular resistance by 9 and 24% respectively, while decreasing significantly glomerular filtration rate and renal plasma flow by 17 and 14% respectively. Enalapril was able to prevent the decline in GFR and the increase in blood pressure induced by CsA. This effect was demonstrated despite a similar increase in renal vascular resistance suggesting a dissociation between changes in glomerular filtration rate and renal vascular resistance during angiotensin converting-enzyme inhibition.

CONCLUSION.: Chronic angiotensin converting-enzyme inhibition could afford some degree of protection against CsA-induced renal dysfunction. Whether these results can be extrapolated to transplant recipients in whom CsA is usually associated to treatment by glucocorticosteroids, deserves further evaluation.

Keywords: cyclosporine A; diabetes mellitus; glomerular filtration rate; renal haemodynamics; kidney tubule; lithium clearance; angiotensin converting enzyme inhibition


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