School of Mathematics and Statistics, University of Sydney, Sydney, NSW, Australia.
Centre for Kidney Research, The Children's Hospital at Westmead, Sydney, NSW, Australia.
Transplantation. 2021 Jun 1;105(6):1225-1237. doi: 10.1097/TP.0000000000003516.
Noninvasive biomarkers may predict adverse events such as acute rejection after kidney transplantation and may be preferable to existing methods because of superior accuracy and convenience. It is uncertain how these biomarkers, often derived from a single study, perform across different cohorts of recipients.
Using a cross-validation framework that evaluates the performance of biomarkers, the aim of this study was to devise an integrated gene signature set that predicts acute rejection in kidney transplant recipients. Inclusion criteria were publicly available datasets of gene signatures that reported acute rejection episodes after kidney transplantation. We tested the predictive probability for acute rejection using gene signatures within individual datasets and validated the set using other datasets. Eight eligible studies of 1454 participants, with a total of 512 acute rejections episodes were included.
All sets of gene signatures had good positive and negative predictive values (79%-96%) for acute rejection within their own cohorts, but the predictability reduced to <50% when tested in other independent datasets. By integrating signature sets with high specificity scores across all studies, a set of 150 genes (included CXCL6, CXCL11, OLFM4, and PSG9) which are known to be associated with immune responses, had reasonable predictive values (varied between 69% and 90%).
A set of gene signatures for acute rejection derived from a specific cohort of kidney transplant recipients do not appear to provide adequate prediction in an independent cohort of transplant recipients. However, the integration of gene signature sets with high specificity scores may improve the prediction performance of these markers.
非侵入性生物标志物可预测肾移植后的急性排斥反应等不良事件,并且由于准确性和便利性更高,可能优于现有方法。这些生物标志物通常来自单一研究,其在不同受者队列中的表现尚不确定。
本研究使用交叉验证框架评估生物标志物的性能,旨在设计一个综合基因特征集,以预测肾移植受者的急性排斥反应。纳入标准为公开的基因特征数据集,这些数据集报告了肾移植后急性排斥反应发作。我们使用单个数据集中的基因特征测试了急性排斥反应的预测概率,并使用其他数据集验证了该特征集。共纳入了 8 项符合条件的研究,共纳入了 1454 名患者,总计 512 例急性排斥反应。
所有基因特征集在各自的队列中对急性排斥反应都具有良好的阳性和阴性预测值(79%-96%),但在其他独立数据集中测试时,预测能力降低至<50%。通过整合所有研究中特异性评分较高的特征集,一组 150 个基因(包括 CXCL6、CXCL11、OLFM4 和 PSG9),已知与免疫反应相关,具有合理的预测值(在 69%-90%之间变化)。
从特定队列的肾移植受者中得出的一组急性排斥反应基因特征似乎无法在独立队列的移植受者中提供充分的预测。然而,整合特异性评分较高的基因特征集可能会提高这些标志物的预测性能。