Podocyte Number in Normotensive Type 1 Diabetic Patients With Albuminuria

Kathryn White(Newcastle University), Rudolf W. Bilous(Newcastle University), Sally M. Marshall(Newcastle University), Meguid El Nahas(Northern General Hospital), Giuseppe Remuzzi(Mario Negri Institute for Pharmacological Research), Giampiero Piras(Azienda Ospedaliera G. Brotzu), Salvatore De Cosmo(Casa Sollievo della Sofferenza), Giancarlo Viberti(Guy's Hospital), on behalf of the European Study for the Prevention of Renal Disease in Type 1 Diabetes (ESPRIT)
Diabetes
October 1, 2002
Cited by 312Open Access
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Abstract

We estimated glomerular cell number in 50 normotensive type 1 diabetic patients with raised albumin excretion rate (AER) and investigated any change after 3 years in a subgroup of 16 placebo-treated patients. Biopsies from 10 normal kidney donors were used as controls. Mesangial and endothelial cell number was increased in the 50 diabetic patients at the start of the study compared with control subjects. There was no difference in podocyte number. Glomerular volume was increased in diabetic patients, but surface area of glomerular basement membrane (GBM) underlying the podocytes did not differ between groups. AER correlated positively with mesangial cell number in microalbuminuric patients (r = 0.44, P = 0.012) and negatively with podocyte number in proteinuric patients (r = -0.48, P = 0.040). In the 16 placebo-treated patients, glomerular volume increased after 3 years owing to matrix accumulation and increased GBM surface area. Although overall cell number did not differ significantly from baseline, the decrease in podocyte number during follow-up correlated with AER at follow-up (r = -0.72, P = 0.002). In conclusion, cross-sectional analysis of podocyte number in type 1 diabetic patients with raised AER but normal blood pressure shows no significant reduction compared with nondiabetic control subjects. Longitudinal data provide evidence for an association between podocyte loss and AER, but whether cellular changes are a response to, a cause of, or concomitant with the progression of nephropathy remains uncertain.


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