ElEVATE: an innovative study design to assess the efficacy, safety, and evolution of cardiovascular parameters in de novo kidney transplant recipients after early conversion from a calcineurin inhibitor to everolimus

IF 1.4 Q4 MEDICINE, RESEARCH & EXPERIMENTAL
M. Giet, J. Cruzado, J. W. Fijter, H. Holdaas, Z. Wang, A. Speziale, G. Junge
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引用次数: 2

Abstract

Progressive decline in allograft function and cardiovascular mortality after kidney transplantation remain major clinical challenges that can potentially be addressed by the mammalian target of rapamycin (mTOR) inhibitors, everolimus and sirolimus. mTOR inhibitors maintain immunosuppressive efficacy after minimization of calcineurin inhibitor (CNI) therapy and can achieve significant long-term improvements in renal function. Recently, data have accumulated that suggest mTOR inhibitors may offer cardioprotective effects. In animal models, inhibition of mTOR leads to regression of cardiac hypertrophy, and the limited data consistently point to a remodeling benefit following heart transplantation. Experimentally, mTOR inhibitors restrict atherogenesis, confirmed clinically by intravascular ultrasound data demonstrating lower rates of transplant vasculopathy in heart transplant recipients on everolimus. Lastly, mTOR inhibitors appear to ameliorate arterial stiffness, a known risk factor for post-transplant cardio- vascular events, but data remain sparse. The ELEVATE study will examine the renal effect of early conversion from CNI therapy to everolimus after kidney transplantation. Key secondary endpoints include the change in left ventricular mass index, the first time this endpoint has been included in a prospective study of an mTOR inhibitor. The occurrence of cardiovascular events will be rigorously documented and pulse wave velocity is being measured in a subpopulation of patients. Results from this innovative trial are awaited with interest.
ElEVATE:一项创新研究,旨在评估从钙调磷酸酶抑制剂早期转换为依维莫司后新肾移植受者心血管参数的有效性、安全性和演变
同种异体移植功能的逐渐下降和肾移植后心血管死亡率仍然是主要的临床挑战,可以通过雷帕霉素(mTOR)抑制剂依维莫司和西罗莫司的哺乳动物靶点来解决。在减少钙调磷酸酶抑制剂(CNI)治疗后,mTOR抑制剂仍能保持免疫抑制效果,并能显著改善肾功能。最近,越来越多的数据表明mTOR抑制剂可能具有心脏保护作用。在动物模型中,抑制mTOR导致心肌肥厚消退,有限的数据一致表明心脏移植后重构获益。实验中,mTOR抑制剂抑制动脉粥样硬化,临床证实血管内超声数据显示依维莫司心脏移植受者移植血管病变发生率较低。最后,mTOR抑制剂似乎可以改善动脉僵硬,这是移植后心血管事件的已知危险因素,但数据仍然很少。ELEVATE研究将检查肾移植后早期从CNI治疗转向依维莫司的肾脏效应。关键的次要终点包括左心室质量指数的变化,这是mTOR抑制剂的前瞻性研究首次纳入该终点。将严格记录心血管事件的发生,并测量患者亚群的脉搏波速度。人们饶有兴趣地等待着这一创新试验的结果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Open Access Journal of Clinical Trials
Open Access Journal of Clinical Trials MEDICINE, RESEARCH & EXPERIMENTAL-
CiteScore
3.90
自引率
0.00%
发文量
2
审稿时长
16 weeks
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