Islet transplantation is associated with an improvement of cardiovascular function in type 1 diabetic kidney transplant patients
Articolo
Data di Pubblicazione:
2005
Abstract:
OBJECTIVE— Cardiovascular mortality and morbidity are major problems in type 1 diabetic
patients with end-stage renal disease (ESRD). The aim of this study was to determine whether
islet transplantation can improve cardiovascular function in these patients.
RESEARCH DESIGN AND METHODS— We assessed various markers of cardiac
function at baseline and 3 years later in a population of 42 type 1 diabetic patients with ESRD
who received a kidney transplant. Seventeen patients then received an islet transplant that had
persistent function as defined by long-term C-peptide secretion (kidney-islet group). Twentyfive
patients did not receive a functioning islet transplant (kidney-only group).
RESULTS— GHb levels were similar in the two groups, whereas the exogenous insulin
requirement was lower in the kidney-islet group with persistent C-peptide secretion. Overall,
cardiovascular parameters improved in the kidney-islet group, but not in the kidney-only group,
with an improvement of ejection fraction (from 68.2 3.5% at baseline to 74.9 2.1% at 3
years posttransplantation, P 0.05) and peak filling rate in end-diastolic volume (EDV) per
second (from 3.87 0.25 to 4.20 0.37 EDV/s, P 0.05). Time to peak filling rate remained
stable in the kidney-islet group but worsened in the kidney-only group (P 0.05). The kidneyislet
group also showed a reduction of both QT dispersion (53.5 4.9 to 44.6 2.9 ms, P
0.05) and corrected QT (QTc) dispersion (67.3 8.3 to 57.2 4.6 ms, P 0.05) with higher
erythrocytes Na-K-ATPase activity. In the kidney-islet group only, both atrial natriuretic
peptide and brain natriuretic peptide levels decreased during the follow-up, with a stabilization
of intima-media thickness.
CONCLUSIONS— Our study showed that type 1 diabetic ESRD patients receiving a kidney
transplant and a functioning islet transplant showed an improvement of cardiovascular function
for up to 3 years of follow-up compared with the kidney-only group, who experienced an early
failure of the islet graft or did not receive an islet graft.
patients with end-stage renal disease (ESRD). The aim of this study was to determine whether
islet transplantation can improve cardiovascular function in these patients.
RESEARCH DESIGN AND METHODS— We assessed various markers of cardiac
function at baseline and 3 years later in a population of 42 type 1 diabetic patients with ESRD
who received a kidney transplant. Seventeen patients then received an islet transplant that had
persistent function as defined by long-term C-peptide secretion (kidney-islet group). Twentyfive
patients did not receive a functioning islet transplant (kidney-only group).
RESULTS— GHb levels were similar in the two groups, whereas the exogenous insulin
requirement was lower in the kidney-islet group with persistent C-peptide secretion. Overall,
cardiovascular parameters improved in the kidney-islet group, but not in the kidney-only group,
with an improvement of ejection fraction (from 68.2 3.5% at baseline to 74.9 2.1% at 3
years posttransplantation, P 0.05) and peak filling rate in end-diastolic volume (EDV) per
second (from 3.87 0.25 to 4.20 0.37 EDV/s, P 0.05). Time to peak filling rate remained
stable in the kidney-islet group but worsened in the kidney-only group (P 0.05). The kidneyislet
group also showed a reduction of both QT dispersion (53.5 4.9 to 44.6 2.9 ms, P
0.05) and corrected QT (QTc) dispersion (67.3 8.3 to 57.2 4.6 ms, P 0.05) with higher
erythrocytes Na-K-ATPase activity. In the kidney-islet group only, both atrial natriuretic
peptide and brain natriuretic peptide levels decreased during the follow-up, with a stabilization
of intima-media thickness.
CONCLUSIONS— Our study showed that type 1 diabetic ESRD patients receiving a kidney
transplant and a functioning islet transplant showed an improvement of cardiovascular function
for up to 3 years of follow-up compared with the kidney-only group, who experienced an early
failure of the islet graft or did not receive an islet graft.
Tipologia CRIS:
1.1 Articolo in rivista
Elenco autori:
Fiorina, P; Gremizzi, C; Maffi, P; Caldara, R; Tavano, D; Monti, L; Socci, C; Folli, F; Fazio, F; Astorri, E; DEL MASCHIO, Alessandro; Secchi, Antonio
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