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通过整合宿主基因表达诊断实现细菌和病毒感染的稳健分类。

Robust classification of bacterial and viral infections via integrated host gene expression diagnostics.

作者信息

Sweeney Timothy E, Wong Hector R, Khatri Purvesh

机构信息

Stanford Institute for Immunity, Transplantation and Infection, Stanford University School of Medicine, Stanford, CA 94305, USA. Biomedical Informatics Research, Stanford University School of Medicine, Stanford, CA 94305, USA.

Division of Critical Care Medicine, Cincinnati Children's Hospital Medical Center and Cincinnati Children's Research Foundation, Cincinnati, OH 45223, USA. Department of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, OH 45267, USA.

出版信息

Sci Transl Med. 2016 Jul 6;8(346):346ra91. doi: 10.1126/scitranslmed.aaf7165.

Abstract

Improved diagnostics for acute infections could decrease morbidity and mortality by increasing early antibiotics for patients with bacterial infections and reducing unnecessary antibiotics for patients without bacterial infections. Several groups have used gene expression microarrays to build classifiers for acute infections, but these have been hampered by the size of the gene sets, use of overfit models, or lack of independent validation. We used multicohort analysis to derive a set of seven genes for robust discrimination of bacterial and viral infections, which we then validated in 30 independent cohorts. We next used our previously published 11-gene Sepsis MetaScore together with the new bacterial/viral classifier to build an integrated antibiotics decision model. In a pooled analysis of 1057 samples from 20 cohorts (excluding infants), the integrated antibiotics decision model had a sensitivity and specificity for bacterial infections of 94.0 and 59.8%, respectively (negative likelihood ratio, 0.10). Prospective clinical validation will be needed before these findings are implemented for patient care.

摘要

改进急性感染的诊断方法,可通过增加对细菌感染患者的早期抗生素治疗,并减少对非细菌感染患者不必要的抗生素使用,从而降低发病率和死亡率。有几个研究小组已使用基因表达微阵列构建急性感染的分类器,但这些方法受到基因集规模、过拟合模型的使用或缺乏独立验证的阻碍。我们采用多队列分析得出一组七个基因,用于可靠地区分细菌感染和病毒感染,随后在30个独立队列中进行了验证。接下来,我们将先前发表的11基因脓毒症MetaScore与新的细菌/病毒分类器相结合,构建了一个综合抗生素决策模型。在对来自20个队列(不包括婴儿)的1057个样本进行的汇总分析中,综合抗生素决策模型对细菌感染的敏感性和特异性分别为94.0%和59.8%(阴性似然比为0.10)。在将这些研究结果应用于患者护理之前,还需要进行前瞻性临床验证。

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