Validation of diagnostic gene sets to identify critically ill patients with sepsis

被引:30
作者
Maslove, David M. [1 ,2 ,3 ]
Shapira, Tal [4 ]
Tyryshkin, Kathrin [5 ]
Veldhoen, Richard A. [2 ]
Marshall, John C. [6 ,7 ]
Muscedere, John [1 ,3 ]
机构
[1] Queens Univ, Dept Crit Care Med, Kingston, ON, Canada
[2] Queens Univ, Dept Med, Kingston, ON, Canada
[3] Queens Univ, Kingston Hlth Sci Ctr, Kingston, ON, Canada
[4] Queens Univ, Sch Comp, Kingston, ON, Canada
[5] Queens Univ, Dept Pathol & Mol Med, Kingston, ON, Canada
[6] St Michaels Hosp, Li Ka Shing Knowledge Inst, Crit Illness & Injury Res Ctr, Toronto, ON, Canada
[7] Univ Toronto, Dept Surg, Toronto, ON, Canada
关键词
Sepsis; Critical care; Gene expression; Precision medicine; Validation studies; CARE; DEFINITIONS; INFECTION;
D O I
10.1016/j.jcrc.2018.10.028
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
Purpose: Gene expression diagnostics have been proposed to identify critically ill patients with sepsis. Three expression-based scores have been developed, but have not been compared in a prospective validation. We sought to validate these scores using an independent dataset and analysis. Methods: We generated gene expression profiles from 61 critically ill patients. We validated the performance of 3 expression-based sepsis scores including 1) the Sepsis MetaScore (SMS); 2) the SeptiCyte (TM) Lab; and 3) the FAIM3:PLAC8 ratio. Sepsis was identified as the presence of definite. probable, or possible infection in the setting of organ dysfunction (SOFA score >= 2). Results: For all 3 models, scores were significantly different between patients with and without sepsis. Discrimination was highest for the SMS (area under the receiver operating characteristics curve [AUROC 0.80 [95% Cl 0.67-0.92]), with greater confidence in the presence of infection resulting in better model performance (max AUROC 0.93 [0.87-1.0]). Conclusions: All three scores distinguished septic from non-septic ICU patients, with the SMS showing the best performance overall in our cohort. Our results suggest that models developed from the co-analysis of multiple cohorts are more generalizable. Further work is needed to identify expression-based biomarkers of response to specific therapies. (C) 2018 Elsevier Inc. All rights reserved.
引用
收藏
页码:92 / 98
页数:7
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