Plasma Cell-free RNA Signatures of Inflammatory Syndromes in Children

Conor J Loy, Venice Servellita, Alicia Sotomayor-Gonzalez, Andrew Bliss, Joan Lenz, Emma Belcher, Will Suslovic, Jenny Nguyen, Meagan Williams, Miriam Oseguera, Michael Gardiner, Pediatric Emergency Medicine Kawasaki Disease Research Group (PEMKDRG), The CHARMS Study Group, Jong-Ha Choi, Hui-Mien Hsiao, Hao Wang, Jihoon Kim, Chisato Shimizu, Adrianna Tremoulet, Meghan Delaney, Roberta DeBiasi, Christina Rostad, Jane Burns, Charles Chiu, Iwijn De Vlaminck
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Abstract

Inflammatory syndromes, including those caused by infection, are a major cause of hospital admissions among children and are often misdiagnosed because of a lack of advanced molecular diagnostic tools. In this study, we explored the utility of circulating cell-free RNA (cfRNA) in plasma as an analyte for the differential diagnosis and characterization of pediatric inflammatory syndromes. We profiled cfRNA in 370 plasma samples from pediatric patients with a range of inflammatory conditions, including Kawasaki disease (KD), Multisystem Inflammatory Syndrome in Children (MIS-C), viral infections and bacterial infections. We developed machine learning models based on these cfRNA profiles, which effectively differentiated KD from MIS-C - two conditions presenting with overlapping symptoms - with high performance (Test Area Under the Curve (AUC) = 0.97). We further extended this methodology into a multiclass machine learning framework that achieved 81% accuracy in distinguishing among KD, MIS-C, viral, and bacterial infections. We further demonstrated that cfRNA profiles can be used to quantify injury to specific tissues and organs, including the liver, heart, endothelium, nervous system, and the upper respiratory tract. Overall, this study identified cfRNA as a versatile analyte for the differential diagnosis and characterization of a wide range of pediatric inflammatory syndromes.
儿童炎症综合征的血浆无细胞 RNA 信号
炎症综合征,包括由感染引起的炎症综合征,是儿童入院治疗的一个主要原因,但由于缺乏先进的分子诊断工具,常常被误诊。在这项研究中,我们探讨了血浆中循环无细胞 RNA(cfRNA)作为一种分析物对儿科炎症综合征的鉴别诊断和特征描述的作用。我们分析了 370 份儿科炎症患者血浆样本中的 cfRNA,这些炎症患者包括川崎病(KD)、儿童多系统炎症综合征(MIS-C)、病毒感染和细菌感染。我们根据这些 cfRNA 图谱开发了机器学习模型,该模型能有效区分 KD 和 MIS-C(这两种疾病的症状相互重叠),而且性能很高(测试曲线下面积 (AUC) = 0.97)。我们进一步将这一方法扩展到多类机器学习框架中,其区分 KD、MIS-C、病毒和细菌感染的准确率达到 81%。我们进一步证明,cfRNA 图谱可用于量化特定组织和器官的损伤,包括肝脏、心脏、内皮、神经系统和上呼吸道。总之,这项研究发现 cfRNA 是一种多功能分析物,可用于鉴别诊断和描述各种儿科炎症综合征。
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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