Podocyte Number in Normotensive Type 1 Diabetic Patients With Albuminuria

Author:

White Kathryn E.1,Bilous Rudolf W.1,Marshall Sally M.1,El Nahas Meguid2,Remuzzi Giuseppe3,Piras Giampiero4,De Cosmo Salvatore5,Viberti GianCarlo6,

Affiliation:

1. Department of Medicine, Medical School, University of Newcastle upon Tyne, Newcastle upon Tyne, U.K.

2. Sheffield Kidney Institute, Northern General Hospital Trust, Sheffield, U.K.

3. Mario Negri Institute for Pharmacological Research, Bergamo, Italy

4. Diabetes Unit, Hospital Brotzu, Cagliari, Italy

5. Division and Research Unit of Endocrinology, “Casa Sollievo della Sofferenza” Hospital, San Giovanni Rotondo, Italy

6. Department of Diabetes, Endocrinology & Internal Medicine, Guy’s Hospital, King’s College London, London, U.K.

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.

Publisher

American Diabetes Association

Subject

Endocrinology, Diabetes and Metabolism,Internal Medicine

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