Diabetes Care 26:1129-1136, 2003
© 2003 by the American Diabetes Association, Inc.
Emerging Treatments and Technologies Original Article |
Long-Term Beneficial Effect of Islet Transplantation on Diabetic Macro-/Microangiopathy in Type 1 Diabetic Kidney-Transplanted Patients
Paolo Fiorina, MD1,
Franco Folli, MD1,
Federico Bertuzzi, MD1,
Paola Maffi, MD1,
Giovanna Finzi, MB2,
Massimo Venturini, MD3,
Carlo Socci, MD4,
Alberto Davalli, MD1,
Elena Orsenigo, MD4,
Lucilla Monti, MD1,
Luca Falqui, MD1,
Silvia Uccella, MD2,
Stefano La Rosa, MD2,
Luciana Usellini, MB2,
Giuliana Properzi, MD5,
Valerio Di Carlo, MD4,6,
Alessandro Del Maschio, MD3,6,
Carlo Capella, MD2 and
Antonio Secchi, MD1,6
1 Department of Internal Medicine I, San Raffaele Scientific Institute, Milan, Italy
2 Department of Pathology, Insubria University, Varese, Italy
3 Department of Radiology, San Raffaele Scientific Institute, Milan, Italy
4 Department of General Surgery, San Raffaele Scientific Institute, Milan, Italy
5 Department of Medicine, LAquila University, LAquila, Italy
6 Vita e Salute-San Raffaele University, Milan, Italy
OBJECTIVEOur aim was to evaluate the long-term effects of transplanted islets on diabetic macro-/microangiopathy in type 1 diabetic kidney-transplanted patients.
RESEARCH DESIGN AND METHODSA total of 34 type 1 diabetic kidney-transplanted patients underwent islet transplantation and were divided into two groups: successful islet-kidney transplantation (SI-K; 21 patients, fasting C-peptide serum concentration >0.5 ng/ml for >1 year) and unsuccessful islet-kidney transplantation (UI-K; 13 patients, fasting C-peptide serum concentration <0.5 ng/ml). Patients cumulative survival, cardiovascular death rate, and atherosclerosis progression were compared in the two groups. Skin biopsies, endothelial dependent dilation (EDD), nitric oxide (NO) levels, and atherothrombotic risk factors [von Willebrand factor (vWF) and D-dimer fragment (DDF)] were studied cross-sectionally.
RESULTSThe SI-K group showed a significant better patient survival rate (SI-K 100, 100, and 90% vs. UI-K 84, 74, and 51% at 1, 4, and 7 years, respectively, P = 0.04), lower cardiovascular death rate (SI-K 1/21 vs. UI-K 4/13, 2 = 3.9, P = 0.04), and lower intima-media thickness progression than the UI-K group (SI-K group: 13 years -13 ± 30 µm vs. UI-K group: 13 years 245 ± 20 µm, P = 0.03) with decreased signs of endothelial injuring at skin biopsy. Furthermore, the SI-K group showed a higher EDD than the UI-K group (EDD: SI-K 7.8 ± 4.5% vs. UI-K 0.5 ± 2.7%, P = 0.02), higher basal NO (SI-K 42.9 ± 6.5 vs. UI-K 20.2 ± 6.8 µmol/l, P = 0.02), and lower levels of vWF (SI-K 138.6 ± 15.3 vs. UI-K 180.6 ± 7.0%, P = 0.02) and DDF (SI-K 0.61 ± 0.22 vs. UI-K 3.07 ± 0.68 µg/ml, P < 0.01). C-peptide-to-creatinine ratio correlated positively with EDD and NO and negatively with vWF and DDF.
CONCLUSIONSSuccessful islet transplantation improves survival, cardiovascular, and endothelial function in type 1 diabetic kidney-transplanted patients.
Abbreviations: DBP, diastolic blood pressure DDF, D-dimer fragment ecNOs, endothelial constitutive nitric oxide synthase EDD, endothelial dependent dilation IMT, intima-media thickness SBP, systolic blood pressure SI-K, successful islet-kidney transplantation UI-K, unsuccessful islet-kidney transplantation vWF, von Willebrand factor

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Copyright © 2003 by the American Diabetes Association.
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