PMID- 21094806 OWN - NLM STAT- MEDLINE DCOM- 20110307 LR - 20211203 IS - 1873-2623 (Electronic) IS - 0041-1345 (Linking) VI - 42 IP - 9 DP - 2010 Nov TI - Low-dose calcineurin inhibitor regimen combined with mammalian target of rapamycin inhibitors preserves kidney functions in renal transplant recipients without allograft nephropathy. PG - 3513-6 LID - 10.1016/j.transproceed.2010.08.043 [doi] AB - OBJECTIVE: The present study was designed to investigate the effect of low-dose calcineurin inhibitor (CNI) tacrolimus combined with a mammalian target of rapamycin (mTOR) inhibitor on renal function in transplant recipients without allograft nephropathy. PATIENTS AND METHODS: Twelve patients including seven men (58.3%) of overall mean age of 34.8 +/- 14.1 years underwent renal transplantation and were switched to a new second-line treatment of low-dose CNI combined with an mTOR inhibitor, either sirolimus or everolimus. RESULTS: The underlying cause of renal failure was not clear in half of the cases; for the others it was chronic glomerulonephritis, diabetic nephropathy, polycystic kidney disease, or hypovolemia. After 6 months of the new therapy, there was a significant increase in calculated creatinine clearance levels compared to baseline (75.5 +/- 21.9 vs 89.6 +/- 19.1 mL/min; P < .001), but no significant change in serum creatinine (1.3 +/- 0.4 vs 1.2 +/- 0.3 mg/dL) or urinary protein excretion (187.5 +/- 142.0 vs 394.0 +/- 326.4 mg/g). For almost all patients, proteinuria remained stable, but in two patients, it developed but responded to enalapril treatment. Dose decrement was required for four patients with hyperlipidemia (50%); one patient experienced new-onset hyperlipidemia that responded to treatment. One patient developed a urinary tract infection that responded to antibiotic treatment. None of the patients developed an acute rejection episode. CONCLUSION: Low-dose CNI combined with an mTOR inhibitor, as a replacement for mycophenolate mofetil or enteric-coated mycophenolate sodium, seemed to prevent renal dysfunction for at least 6 months among renal transplant patients without allograft nephropathy. CI - Copyright (c) 2010. Published by Elsevier Inc. FAU - Kacar, S AU - Kacar S AD - Kent Hospital, Izmir, Turkey. hilmiserdar@superonline.com FAU - Gurkan, A AU - Gurkan A FAU - Karaca, C AU - Karaca C FAU - Varilsuha, C AU - Varilsuha C FAU - Tilif, S AU - Tilif S LA - eng PT - Journal Article PL - United States TA - Transplant Proc JT - Transplantation proceedings JID - 0243532 RN - 0 (Biomarkers) RN - 0 (Calcineurin Inhibitors) RN - 0 (Immunosuppressive Agents) RN - 9HW64Q8G6G (Everolimus) RN - AYI8EX34EU (Creatinine) RN - EC 2.7.1.1 (MTOR protein, human) RN - EC 2.7.11.1 (TOR Serine-Threonine Kinases) RN - W36ZG6FT64 (Sirolimus) RN - WM0HAQ4WNM (Tacrolimus) SB - IM MH - Adult MH - Biomarkers/blood MH - *Calcineurin Inhibitors MH - Creatinine/blood MH - Drug Substitution MH - Drug Therapy, Combination MH - Everolimus MH - Female MH - Humans MH - Hyperlipidemias/etiology MH - Immunosuppressive Agents/*administration & dosage/adverse effects MH - Kidney/*drug effects/metabolism/physiopathology MH - *Kidney Transplantation/adverse effects MH - Male MH - Middle Aged MH - Proteinuria/etiology MH - Sirolimus/administration & dosage/adverse effects/*analogs & derivatives MH - TOR Serine-Threonine Kinases/*antagonists & inhibitors MH - Tacrolimus/*administration & dosage/adverse effects MH - Time Factors MH - Transplantation, Homologous MH - Treatment Outcome MH - Turkey MH - Urinary Tract Infections/etiology MH - Young Adult EDAT- 2010/11/26 06:00 MHDA- 2011/03/08 06:00 CRDT- 2010/11/25 06:00 PHST- 2010/03/22 00:00 [received] PHST- 2010/06/04 00:00 [revised] PHST- 2010/08/26 00:00 [accepted] PHST- 2010/11/25 06:00 [entrez] PHST- 2010/11/26 06:00 [pubmed] PHST- 2011/03/08 06:00 [medline] AID - S0041-1345(10)01270-4 [pii] AID - 10.1016/j.transproceed.2010.08.043 [doi] PST - ppublish SO - Transplant Proc. 2010 Nov;42(9):3513-6. doi: 10.1016/j.transproceed.2010.08.043.