Long‐term data on cardiovascular (CV) outcome of renal transplant recipients (RTR) on mTOR‐i (mammalian Target Of Rapamycin‐inhibitors) are scarce. In a sub‐study of the MECANO trial we investigated changes in… Click to show full abstract
Long‐term data on cardiovascular (CV) outcome of renal transplant recipients (RTR) on mTOR‐i (mammalian Target Of Rapamycin‐inhibitors) are scarce. In a sub‐study of the MECANO trial we investigated changes in intima media thickness (IMT), CV risk profile, Major Adverse CV Events (MACE) and survival in RTR on a mTORi versus CNI based regimen. Patients (enrolled 361) were treated with (basiliximab) and triple IS (CsA‐Cyclosporine A‐(C), MPS (M), prednisolone (P)). At M6 patients were randomized (n = 224) to the CsA group (C, P, N = 89), MPS group (M, P, N = 39) EVL group (Everolimus, P, N = 96). At week 2, M6 and M 24, IMT measurements of the Common Carotid Artery were performed. Cardiovascular risk factors were assessed at baseline, 6 and 24 months of follow‐up. Seven years survival and MACE‐free survival probability were calculated by the Cardiovascular Risk Calculator for RTR. After 7 years of follow‐up, incidence of cardiovascular events and patient survival were assessed. Mean IMT at baseline (N = 192), was 0.64 ± 0.14 mm. At M6 (N = 158), 0.66 ± 0.15, M24 IMT was 0.68 ± 0.15 (N = 95). No significant differences between groups concerning IMT, true CV events and mortality, CV risk profile, predicted MACE/Mortality were found between mTORi and CNI‐based regimen after 7 years of follow‐up.
               
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