[Changes in the pre-transplant bone-mineral metabolism do not affect the initial progress of the renal graft]. / Las alteraciones del metabolismo óseo-mineral pretrasplante no influyen en la evolución inicial del injerto renal.

BACKGROUND: Abnormalities in serum calcium, phosphate, and Parathyroid Hormone (PTH) concentrations are common in patients with chronic kidney disease and have been associated with increased morbidity and mortality. One of the most common problems in the first weeks after renal transplantation is Delayed Graft Function (DGF). There are several well-known risk factors for DGF development, but the role of calcium phosphate-PTH homeostasis as a risk factor for early graft dysfunction is controversial. This issue was addressed in the current study. METHODS: Pretransplant PTH, calcium and phosphate values were gathered in 449 patients that received a renal transplant in our center between 1994 and 2007. Other variables expected to influence the risk for delayed graft function were included from the clinical charts. RESULTS: The incidence of DGF was 27.3%. DGF development was significantly associated with recipient age, type and need of renal replacement therapy, peak panel reactive antibodies, transfusion number and donor age. There were no significant differences in the mean pretransplant values of calcium (9.4 +/- 1.0 vs. 9.5 +/- 0.9 mg/dl, p = 0.667), phosphate (5.7 +/- 1.8 vs. 5.5 +/- 1.5 mg/dl, p = 0.457), calcium-phosphate product (53.5 +/- 17.2 vs. 51.8 +/- 14.6 mg(2)/dl(2), p = 0.413) and PTH (315 +/- 312 vs. 340 +/- 350 pg/ml, p = 0.530) between patients with and without DGF. CONCLUSIONS: In our study population pretransplant serum PTH, calcium and phosphorus levels have no influence on the risk for DGF.

Las alteraciones del metabolismo óseo-mineral pretrasplante no influyen en la evolución inicial del injerto renal / No disponible

Antecedentes: el Retraso en la Función del Injerto (RFI) es uno delos problemas más frecuentes en las primeras semanas del trasplante renal, afectando a su evolución. Conocer los factores de riesgo de RFI puede ayudar a reducir su incidencia. Las alteraciones en los niveles séricos de calcio, fósforo y Hormona Paratiroidea (HPT) son muy frecuentes en los pacientes en lista de espera de trasplante y podrían favorecer la aparición de RFI. Sin embargo, diversos estudios que han analizado la relación entre los niveles pretrasplante de calcio, fósforo y HPT y el desarrollo de RFI han obtenido resultados dispares que no permiten confirmar ni descartar que influyan en el mismo. Métodos: estudiamos los valores pretrasplante de calcio, fósforo y HPT en 449 pacientes trasplantados renales realizados entre 1994 y 2007. Se definió RFI en aquellos pacientes que precisaron diálisis durante la primera semana postrasplante. De las historias clínicas se recogieron los datos clínicos y analíticos relacionados con RFI. Resultados: un 27,3%presentó RFI. Los factores significativos de riesgo para desarrollar RFI fueron la edad del receptor, el tipo y la necesidad de tratamiento sustitutivo renal, el título de anticuerpos anti-HLA máximos, el número de trasfusiones pretrasplante y la edad del donante. No detectamos diferencias significativas en los valores medios de calcio (9,4 ± 1,0 vs. 9,5 ± 0,9 mg/dl, p = 0,667), fósforo(5,7 ± 1,8 vs. 5,5 ± 1,5 mg/dl, p = 0,457), producto fosfocálcico (53,5± 17,2 vs. 51,8 ± 14,6 mg2/dl2, p = 0,413) y HPTi (315 ± 312 vs. 340± 350 pg/ml, p = 0,530) en los pacientes con y sin RFI. Conclusiones: en nuestro estudio, los parámetros séricos pretrasplante del metabolismo óseo-mineral no favorecen el desarrollo de RFI (AU)

Background: abnormalities in serum calcium, phosphate, and Parathyroid Hormone (HPT) concentrations are common in patients with chronic kidney disease and have been associated with increased morbidity and mortality. One of the most common problems in the first weeks after renal transplantation is Delayed Graft Function (DGF). There are several well-known risk factors for DGF development, but the role of calciumphosphate-HPT homeostasis as a risk factor for early graft dysfunction is controversial. This issue was addressed in the current study. Methods: Pretransplant HPT, calcium and phosphate values were gathered in 449patients that received a renal transplant in our center between 1994 and 2007. Other variables expected to influence the risk for delayed graft function wereincluded from the clinical charts. Results: The incidence of DGF was 27.3%. DGF development was significantly associated with recipient age, type and need of renal replacement therapy, peak panel reactive antibodies, transfusion number and donor age. There were no significant differences in the mean pretransplant values of calcium (9.4 ± 1.0 vs. 9.5 ± 0.9 mg/dl, p = 0.667),phosphate (5.7 ± 1.8 vs. 5.5 ± 1.5 mg/dl, p = 0.457),calcium-phosphate product (53.5 ± 17.2 vs. 51.8 ± 14.6mg2/dl2, p = 0.413) and HPT (315 ± 312 vs. 340 ± 350pg/ml, p = 0.530) between patients with and without DGF. Conclusions: In our study population pretransplant serum HPT, calcium and phosphorus levels have no influence on the risk for DGF (AU)

Prevention of murine lupus disease in (NZBxNZW)F1 mice by sirolimus treatment.

Sirolimus is a new immunosuppressive drug used to avoid allograft rejection. The immunosuppressive effect of sirolimus is due to inhibition of the mammalian target of rapamycin, necessary for the proliferation and clonal expansion of activated T-cells. Because T-cells play a central role in the pathogenesis of autoimmune disease developed in (NZBxNZW)F1 mice, we evaluated the therapeutic use of sirolimus in such mice. (NZBxNZW)F1 female mice received 1mg/kg/day of sirolimus from 12 to 37 weeks of age. The development of autoimmune disease was evaluated by measuring the serum levels of auto-antibodies (autoAbs) and their immunoglobulin isotypes, prevalence of glomerulonephritis and mortality rates. Sirolimus directly inhibited production of autoAbs, glomerular deposits of immunoglobulins and development of proteinuria; also the survival of these mice was prolonged. Our results demonstrate the beneficial effects of sirolimus in preventing the development of lupus disease in (NZBxNZW)F1 female mice.