Author
Listed:
- Timothy E. Sweeney
(Stanford University School of Medicine
Stanford University School of Medicine
Inflammatix Inc.)
- Thanneer M. Perumal
(Sage Bionetworks)
- Ricardo Henao
(Duke University
Duke University)
- Marshall Nichols
(Duke University)
- Judith A. Howrylak
(Penn State Milton S. Hershey Medical Center)
- Augustine M. Choi
(Cornell Medical Center)
- Jesús F. Bermejo-Martin
(Hospital Clínico Universitario de Valladolid/IECSCYL)
- Raquel Almansa
(Hospital Clínico Universitario de Valladolid/IECSCYL)
- Eduardo Tamayo
(Hospital Clínico Universitario de Valladolid/IECSCYL)
- Emma E. Davenport
(Harvard Medical School
Partners Center for Personalized Genetic Medicine
Broad Institute of MIT and Harvard)
- Katie L. Burnham
(University of Oxford)
- Charles J. Hinds
(Queen Mary University)
- Julian C. Knight
(University of Oxford)
- Christopher W. Woods
(Duke University
Duke University
Durham Veteran’s Affairs Health Care System)
- Stephen F. Kingsmore
(Rady Children’s Institute for Genomic Medicine)
- Geoffrey S. Ginsburg
(Duke University)
- Hector R. Wong
(Cincinnati Children’s Hospital Medical Center and Cincinnati Children’s Research Foundation
University of Cincinnati College of Medicine)
- Grant P. Parnell
(Westmead Institute for Medical Research)
- Benjamin Tang
(Westmead Institute for Medical Research
Nepean Hospital, Sydney, Australia
University of Sydney
Marie Bashir Institute for Infectious Diseases and Biosecurity)
- Lyle L. Moldawer
(University of Florida College of Medicine)
- Frederick E. Moore
(University of Florida College of Medicine)
- Larsson Omberg
(Sage Bionetworks)
- Purvesh Khatri
(Stanford University School of Medicine
Stanford University School of Medicine)
- Ephraim L. Tsalik
(Duke University
Duke University
Durham Veteran’s Affairs Health Care System)
- Lara M. Mangravite
(Sage Bionetworks)
- Raymond J. Langley
(University of South Alabama)
Abstract
Improved risk stratification and prognosis prediction in sepsis is a critical unmet need. Clinical severity scores and available assays such as blood lactate reflect global illness severity with suboptimal performance, and do not specifically reveal the underlying dysregulation of sepsis. Here, we present prognostic models for 30-day mortality generated independently by three scientific groups by using 12 discovery cohorts containing transcriptomic data collected from primarily community-onset sepsis patients. Predictive performance is validated in five cohorts of community-onset sepsis patients in which the models show summary AUROCs ranging from 0.765–0.89. Similar performance is observed in four cohorts of hospital-acquired sepsis. Combining the new gene-expression-based prognostic models with prior clinical severity scores leads to significant improvement in prediction of 30-day mortality as measured via AUROC and net reclassification improvement index These models provide an opportunity to develop molecular bedside tests that may improve risk stratification and mortality prediction in patients with sepsis.
Suggested Citation
Timothy E. Sweeney & Thanneer M. Perumal & Ricardo Henao & Marshall Nichols & Judith A. Howrylak & Augustine M. Choi & Jesús F. Bermejo-Martin & Raquel Almansa & Eduardo Tamayo & Emma E. Davenport & K, 2018.
"A community approach to mortality prediction in sepsis via gene expression analysis,"
Nature Communications, Nature, vol. 9(1), pages 1-10, December.
Handle:
RePEc:nat:natcom:v:9:y:2018:i:1:d:10.1038_s41467-018-03078-2
DOI: 10.1038/s41467-018-03078-2
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