TY - JOUR
T1 - Conversion from cyclosporine to tacrolimus improves quality-of-life indices, renal graft function and cardiovascular risk profile
AU - Artz, Marika A.
AU - Boots, Johannes M.M.
AU - Ligtenberg, Gerry
AU - Roodnat, Joke I.
AU - Christiaans, Maarten H.L.
AU - Vos, Pieter F.
AU - Moons, Philip
AU - Borm, George
AU - Hilbrands, Luuk B.
PY - 2004/6
Y1 - 2004/6
N2 - Long-term use of cyclosporine after renal transplantation results in nephrotoxicity and an increased cardiovascular risk profile. Tacrolimus may be more favorable in this respect. In this randomized controlled study in 124 renal-transplant patients, the effects of conversion from cyclosporine to tacrolimus on renal function, cardiovascular risk factors, and perceived side-effects were investigated after a follow-up of 2 years. After conversion from cyclosporine to tacrolimus renal function remained stable, whereas continuation of cyclosporine was accompanied by a rise in serum creatinine from 142 ± 48 μmol/L to 157 ± 62 μmol/L (p < 0.05 comparing both groups). Conversion to tacrolimus resulted in a sustained reduction in systolic and diastolic blood pressure, and a sustained improvement in the serum lipid profile, leading to a reduction in the Framingham risk score from 5.7 ± 4.3 to 4.8 ± 5.3 (p < 0.05). Finally, conversion to tacrolimus resulted in decreased scores for occurrence of and distress due to side-effects. In conclusion, conversion from cyclosporine to tacrolimus in stable renal-transplant patients is beneficial with respect to renal function, cardiovascular risk profile, and side-effects. Therefore, for most renal transplant patients tacrorimus will be the drug of choice when long-term treatment with a calcineurin inhibitor is indicated.
AB - Long-term use of cyclosporine after renal transplantation results in nephrotoxicity and an increased cardiovascular risk profile. Tacrolimus may be more favorable in this respect. In this randomized controlled study in 124 renal-transplant patients, the effects of conversion from cyclosporine to tacrolimus on renal function, cardiovascular risk factors, and perceived side-effects were investigated after a follow-up of 2 years. After conversion from cyclosporine to tacrolimus renal function remained stable, whereas continuation of cyclosporine was accompanied by a rise in serum creatinine from 142 ± 48 μmol/L to 157 ± 62 μmol/L (p < 0.05 comparing both groups). Conversion to tacrolimus resulted in a sustained reduction in systolic and diastolic blood pressure, and a sustained improvement in the serum lipid profile, leading to a reduction in the Framingham risk score from 5.7 ± 4.3 to 4.8 ± 5.3 (p < 0.05). Finally, conversion to tacrolimus resulted in decreased scores for occurrence of and distress due to side-effects. In conclusion, conversion from cyclosporine to tacrolimus in stable renal-transplant patients is beneficial with respect to renal function, cardiovascular risk profile, and side-effects. Therefore, for most renal transplant patients tacrorimus will be the drug of choice when long-term treatment with a calcineurin inhibitor is indicated.
UR - http://www.scopus.com/inward/record.url?scp=2942532619&partnerID=8YFLogxK
U2 - 10.1111/j.1600-6143.2004.00427.x
DO - 10.1111/j.1600-6143.2004.00427.x
M3 - Article
C2 - 15147428
SN - 1600-6135
VL - 4
SP - 937
EP - 945
JO - American Journal of Transplantation
JF - American Journal of Transplantation
IS - 6
ER -