Heart and Lung Transplant Unit, St. Vincent's Hospital, Sydney, Australia.
Heart and Lung Transplant Unit, St. Vincent's Hospital, Sydney, Australia; Victor Chang Cardiac Research Institute.
JACC Heart Fail. 2021 Apr;9(4):301-313. doi: 10.1016/j.jchf.2021.01.007.
This study aimed to determine the safety and efficacy of combined low-dose everolimus and low-dose tacrolimus compared with standard-dose tacrolimus in attenuating left ventricular hypertrophy (LVH) after orthotopic heart transplantation (OHT).
Calcineurin inhibitors (CNIs) such as tactrolimus are important in preventing cardiac allograft rejection and reducing mortality after OHT. However CNIs are causatively linked to the development of LVH, and are associated with nephrotoxicity and vasculopathy. CNI-sparing agents such as everolimus have been hypothesized to inhibit adverse effects of CNIs.
In this prospective, randomized, open-label study, OHT recipients were randomized at 12 weeks after OHT to a combination of low-dose everolimus and tacrolimus (the RADTAC group) or standard-dose tacrolimus (the TAC group), with both groups coadministered mycophenolate and prednisolone. The primary endpoint was LVH indexed as the change in left ventricular mass (ΔLVM) by cardiovascular magnetic resonance (CMR) imaging from 12 to 52 weeks. Secondary endpoints included CMR-based myocardial performance, T1 fibrosis mapping, blood pressure, and renal function. Safety endpoints included episodes of allograft rejection and infection.
Forty stable OHT recipients were randomized. Recipients in the RADTAC group had significantly lower tacrolimus levels compared with the TAC group (6.5 ± 3.5 μg/l vs. 8.6 ± 2.8 μg/l; p = 0.02). The mean everolimus level in the RADTAC group was 4.2 ± 1.7 μg/l. A significant reduction in LVM was observed in the RADTAC group compared with an increase in LVM in the TAC group (ΔLVM = -13.0 ± 16.8 g vs. 2.1 ± 8.4 g; p < 0.001). Significant differences were also noted in secondary endpoints measuring function and fibrosis (Δ circumferential strain = -2.9 ± 2.8 vs. 2.1 ± 2.3; p < 0.001; ΔT1 mapping values = -32.7 ± 51.3 ms vs. 26.3 ± 90.4 ms; p = 0.003). No significant differences were observed in blood pressure (Δ mean arterial pressure = 4.2 ± 18.8 mm Hg vs. 2.8 ± 13.8 mm Hg; p = 0.77), renal function (Δ creatinine = 3.1 ± 19.9 μmol/l vs. 9 ± 21.8 μmol/l; p = 0.31), frequency of rejection episodes (p = 0.69), or frequency of infections (p = 0.67) between groups.
The combination of low-dose everolimus and tacrolimus compared with standard-dose tacrolimus safely attenuates LVH in the first year after cardiac transplantation with an observed reduction in CMR-measured fibrosis and an improvement in myocardial strain.
本研究旨在确定与标准剂量他克莫司相比,小剂量依维莫司联合小剂量他克莫司在减轻原位心脏移植(OHT)后左心室肥厚(LVH)方面的安全性和有效性。
钙调神经磷酸酶抑制剂(CNIs)如他克莫司在预防心脏移植物排斥和降低 OHT 后死亡率方面非常重要。然而,CNIs 与 LVH 的发生有因果关系,并与肾毒性和血管病变有关。依维莫司等 CNI 节约剂被假设可以抑制 CNI 的不良反应。
在这项前瞻性、随机、开放标签研究中,OHT 受者在 OHT 后 12 周时随机分为低剂量依维莫司联合他克莫司(RADTAC 组)或标准剂量他克莫司(TAC 组),两组均联合使用吗替麦考酚酯和泼尼松龙。主要终点是通过心血管磁共振(CMR)成像从 12 周到 52 周的左心室质量(ΔLVM)变化来评估 LVH。次要终点包括基于 CMR 的心肌性能、T1 纤维化映射、血压和肾功能。安全性终点包括移植物排斥和感染发作。
40 例稳定的 OHT 受者被随机分组。RADTAC 组的他克莫司水平明显低于 TAC 组(6.5±3.5μg/l 比 8.6±2.8μg/l;p=0.02)。RADTAC 组的平均依维莫司水平为 4.2±1.7μg/l。与 TAC 组的 LVM 增加相比,RADTAC 组的 LVM 显著减少(ΔLVM=-13.0±16.8 g 比 2.1±8.4 g;p<0.001)。在测量功能和纤维化的次要终点中也观察到显著差异(Δ圆周应变=-2.9±2.8 比 2.1±2.3;p<0.001;ΔT1 映射值=-32.7±51.3 ms 比 26.3±90.4 ms;p=0.003)。两组之间的血压(Δ平均动脉压=4.2±18.8 mm Hg 比 2.8±13.8 mm Hg;p=0.77)、肾功能(Δ肌酐=3.1±19.9 μmol/l 比 9±21.8 μmol/l;p=0.31)、排斥发作频率(p=0.69)或感染频率(p=0.67)均无显著差异。
与标准剂量他克莫司相比,小剂量依维莫司联合小剂量他克莫司在心脏移植后第一年安全地减轻 LVH,并观察到 CMR 测量的纤维化减少和心肌应变改善。