Key result
Early conversion from cyclosporine A to everolimus in renal transplant recipients showed no clinically relevant effect on cardiac function or morphology after 3 years of follow-up.
Why the study?
Does early conversion from cyclosporine A to everolimus improve cardiac function in de novo renal transplant recipients?
RCT (n=39)
randomized
Does early conversion from cyclosporine A to everolimus improve cardiac function in de novo renal transplant recipients?
Early conversion from cyclosporine A to everolimus does not significantly affect long-term cardiac function or morphology in renal transplant recipients.
No cardiac benefit from early CsA-to-everolimus conversion; leaves open whether larger trials confirm effects in renal transplant recipients.
BACKGROUND: In transplant recipients, calcineurin inhibitors (CNIs) are associated with adverse cardiac effects while mTOR inhibitors have been reported to be beneficial. We performed a randomized controlled trial (RCT) in de novo renal transplant recipients examining cardiac responses of everolimus vs. CNI. METHODS: This was a substudy of the three-yr CENTRAL study, an RCT on safety and efficacy of early (week 7 post-engraftment) conversion from cyclosporine A (CsA) to everolimus vs. continued CsA. Thirty-nine recipients [median age 64 yr, (range 31-81)] completed echocardiographic evaluations at baseline, one, and three yr. RESULTS: After three yr, there was no difference between groups in left ventricle (LV) diastolic function, LV systolic function, LV morphology, and blood pressure response. We observed a relevant decrease in LV mass (CsA; 9.6%, p = 0.008, vs. everolimus; 7.0% reduction, p = 0.15), stabilized LV diastolic function, and a trend toward lower systolic blood pressure with 6 mmHg decrease in both arms (CsA, p = 0.08; everolimus, p = 0.14). Diastolic blood pressure was significantly reduced (8 mmHg decrease, p = 0.002) only in everolimus patients. CONCLUSIONS: After three-yr follow-up, no clinically relevant effect on cardiac function of an early conversion from CsA to an everolimus-based immunosuppressive regimen was detected in de novo renal transplant recipients.
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Murbræch et al. (2015) conducted an RCT in de novo renal transplant recipients (n=39). Early conversion to everolimus vs. Continued cyclosporine A (CsA) was evaluated on Left ventricle (LV) diastolic function, LV systolic function, LV morphology, and blood pressure response. Early conversion from cyclosporine A to everolimus in renal transplant recipients showed no clinically relevant effect on cardiac function or morphology after 3 years of follow-up.
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