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移植心脏血管病的虚拟组织学评估:依维莫司的应用——一项多中心试验的结果。

Virtual histology assessment of cardiac allograft vasculopathy following introduction of everolimus--results of a multicenter trial.

机构信息

Department of Cardiology, Oslo University Hospital Rikshospitalet, Oslo, Norway.

出版信息

Am J Transplant. 2012 Oct;12(10):2700-9. doi: 10.1111/j.1600-6143.2012.04234.x. Epub 2012 Sep 7.

Abstract

In this 12-month multicenter Scandinavian study, 78 maintenance heart transplant (HTx) recipients randomized to everolimus with reduced calcineurin inhibitor (CNI) exposure or continued standard CNI-therapy underwent matched virtual histology (VH) examination to evaluate morphological progression of cardiac allograft vasculopathy (CAV). Parallel measurement of a range of inflammatory markers was also performed. A similar rate of quantitative CAV progression was observed in the everolimus (n = 30) and standard CNI group (n = 48) (plaque index 1.9 ± 3.8% and 1.6 ± 3.9%, respectively; p = 0.65). However, VH analysis revealed a significant increase in calcified (2.4 ± 4.0 vs. 0.3 ± 3.1%; p = 0.02) and necrotic component (6.5 ± 8.5 vs. 1.1 ± 8.6%; p = 0.01) among everolimus patients compared to controls. The increase in necrotic and calcified components was most prominent in everolimus patients with time since HTx >5.1 years and was accompanied by a significant increase in levels of von Willebrand (vWF) factor (p = 0.04) and vascular cell adhesion molecule (VCAM) (p = 0.03). Conversion to everolimus and reduced CNI is associated with a significant increase in calcified and necrotic intimal components and is more prominent in patients with a longer time since HTx. A significant increase in vWF and VCAM accompanied these qualitative changes and the prognostic implication of these findings requires further investigation.

摘要

在这项为期 12 个月的斯堪的纳维亚多中心研究中,78 名接受维持性心脏移植(HTx)的患者被随机分为依维莫司联合降低钙调神经磷酸酶抑制剂(CNI)暴露组或继续标准 CNI 治疗组,进行匹配的虚拟组织学(VH)检查,以评估心脏移植血管病(CAV)的形态学进展。同时平行测量了一系列炎症标志物。依维莫司组(n = 30)和标准 CNI 组(n = 48)的定量 CAV 进展率相似(斑块指数分别为 1.9 ± 3.8%和 1.6 ± 3.9%,p = 0.65)。然而,VH 分析显示,依维莫司组的钙化(2.4 ± 4.0%比 0.3 ± 3.1%;p = 0.02)和坏死成分(6.5 ± 8.5%比 1.1 ± 8.6%;p = 0.01)显著增加。与对照组相比,依维莫司组中坏死和钙化成分的增加在 HTx 后时间>5.1 年的患者中最为显著,同时 von Willebrand(vWF)因子(p = 0.04)和血管细胞黏附分子(VCAM)(p = 0.03)水平显著升高。转换为依维莫司和降低 CNI 与钙化和坏死内膜成分的显著增加相关,在 HTx 后时间较长的患者中更为显著。vWF 和 VCAM 的显著增加伴随着这些定性变化,这些发现的预后意义需要进一步研究。

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