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HEARTBiT:一种用于排除成人心脏移植患者急性细胞排斥的转录组学特征。

HEARTBiT: A Transcriptomic Signature for Excluding Acute Cellular Rejection in Adult Heart Allograft Patients.

机构信息

Prevention of Organ Failure (PROOF) Centre of Excellence, Vancouver, British Columbia, Canada.

Prevention of Organ Failure (PROOF) Centre of Excellence, Vancouver, British Columbia, Canada.

出版信息

Can J Cardiol. 2020 Aug;36(8):1217-1227. doi: 10.1016/j.cjca.2019.11.017. Epub 2019 Nov 25.

Abstract

BACKGROUND

Nine mRNA transcripts associated with acute cellular rejection (ACR) in previous microarray studies were ported to the clinically amenable NanoString nCounter platform. Here we report the diagnostic performance of the resulting blood test to exclude ACR in heart allograft recipients: HEARTBiT.

METHODS

Blood samples for transcriptomic profiling were collected during routine post-transplantation monitoring in 8 Canadian transplant centres participating in the Biomarkers in Transplantation initiative, a large (n = 1622) prospective observational study conducted between 2009 and 2014. All adult cardiac transplant patients were invited to participate (median age = 56 [17 to 71]). The reference standard for rejection status was histopathology grading of tissue from endomyocardial biopsy (EMB). All locally graded ISHLT ≥ 2R rejection samples were selected for analysis (n = 36). ISHLT 1R (n = 38) and 0R (n = 86) samples were randomly selected to create a cohort approximately matched for site, age, sex, and days post-transplantation, with a focus on early time points (median days post-transplant = 42 [7 to 506]).

RESULTS

ISHLT ≥ 2R rejection was confirmed by EMB in 18 and excluded in 92 samples in the test set. HEARTBiT achieved 47% specificity (95% confidence interval [CI], 36%-57%) given ≥ 90% sensitivity, with a corresponding area under the receiver operating characteristic curve of 0.69 (95% CI, 0.56-0.81).

CONCLUSIONS

HEARTBiT's diagnostic performance compares favourably to the only currently approved minimally invasive diagnostic test to rule out ACR, AlloMap (CareDx, Brisbane, CA) and may be used to inform care decisions in the first 2 months post-transplantation, when AlloMap is not approved, and most ACR episodes occur.

摘要

背景

在先前的微阵列研究中,与急性细胞排斥(ACR)相关的 9 个 mRNA 转录本被移植到临床可行的 NanoString nCounter 平台上。在这里,我们报告了该血液检测排除心脏移植受者 ACR 的诊断性能:HEARTBiT。

方法

在参与移植生物标志物倡议的 8 个加拿大移植中心进行的常规移植后监测中采集用于转录组分析的血液样本,这是一项在 2009 年至 2014 年期间进行的大型前瞻性观察研究(n=1622)。所有成年心脏移植患者均被邀请参与(中位年龄 56[17 至 71]岁)。排斥状态的参考标准是心肌活检(EMB)组织的组织病理学分级。选择所有局部分级 ISHLT≥2R 排斥样本进行分析(n=36)。随机选择 ISHLT 1R(n=38)和 0R(n=86)样本以创建一个大约与部位、年龄、性别和移植后天数匹配的队列,重点是早期时间点(中位移植后天数 42[7 至 506]天)。

结果

在测试集中,18 份 EMB 证实 ISHLT≥2R 排斥,92 份排除。HEARTBiT 的特异性为 47%(95%置信区间 [CI],36%-57%),灵敏度≥90%,相应的受试者工作特征曲线下面积为 0.69(95%CI,0.56-0.81)。

结论

HEARTBiT 的诊断性能与目前唯一批准的排除 ACR 的微创诊断测试 AlloMap(CareDx,Brisbane,CA)相当,并且可能用于在移植后 2 个月内告知护理决策,当 AlloMap 未获得批准且大多数 ACR 发作发生时。

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