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Unsupervised Analysis of Transcriptomics in Bacterial Sepsis Across Multiple Datasets Reveals Three Robust Clusters.
Sweeney, Timothy E; Azad, Tej D; Donato, Michele; Haynes, Winston A; Perumal, Thanneer M; Henao, Ricardo; Bermejo-Martin, Jesús F; Almansa, Raquel; Tamayo, Eduardo; Howrylak, Judith A; Choi, Augustine; Parnell, Grant P; Tang, Benjamin; Nichols, Marshall; Woods, Christopher W; Ginsburg, Geoffrey S; Kingsmore, Stephen F; Omberg, Larsson; Mangravite, Lara M; Wong, Hector R; Tsalik, Ephraim L; Langley, Raymond J; Khatri, Purvesh.
Affiliation
  • Sweeney TE; Stanford Institute for Immunity, Transplantation and Infection, Stanford University School of Medicine, Stanford, CA.
  • Azad TD; Biomedical Informatics Research, Department of Medicine, Stanford University School of Medicine, Stanford, CA.
  • Donato M; Stanford Institute for Immunity, Transplantation and Infection, Stanford University School of Medicine, Stanford, CA.
  • Haynes WA; Biomedical Informatics Research, Department of Medicine, Stanford University School of Medicine, Stanford, CA.
  • Perumal TM; Stanford Institute for Immunity, Transplantation and Infection, Stanford University School of Medicine, Stanford, CA.
  • Henao R; Biomedical Informatics Research, Department of Medicine, Stanford University School of Medicine, Stanford, CA.
  • Bermejo-Martin JF; Stanford Institute for Immunity, Transplantation and Infection, Stanford University School of Medicine, Stanford, CA.
  • Almansa R; Biomedical Informatics Research, Department of Medicine, Stanford University School of Medicine, Stanford, CA.
  • Tamayo E; Sage Bionetworks, Seattle, WA.
  • Howrylak JA; Center for Applied Genomics and Precision Medicine, Department of Medicine, Duke University, Durham, NC.
  • Choi A; Department of Electrical and Computer Engineering, Duke University, Durham, NC.
  • Parnell GP; Bio Sepsis, Hospital Clínico Universitario de Valladolid/IECSCYL, Valladolid, Spain.
  • Tang B; Bio Sepsis, Hospital Clínico Universitario de Valladolid/IECSCYL, Valladolid, Spain.
  • Nichols M; Bio Sepsis, Hospital Clínico Universitario de Valladolid/IECSCYL, Valladolid, Spain.
  • Woods CW; Division of Pulmonary, Allergy, and Critical Care Medicine, Department of Medicine, Penn State Milton S. Hershey Medical Center, Hershey, PA.
  • Ginsburg GS; Department of Medicine, Cornell Medical Center, New York, NY.
  • Kingsmore SF; Centre for Immunology and Allergy Research, Westmead Institute for Medical Research, Sydney, NSW, Australia.
  • Mangravite LM; Center for Applied Genomics and Precision Medicine, Department of Medicine, Duke University, Durham, NC.
  • Wong HR; Center for Applied Genomics and Precision Medicine, Department of Medicine, Duke University, Durham, NC.
  • Tsalik EL; Division of Infectious Diseases and International Health, Department of Medicine, Duke University, Durham, NC.
  • Langley RJ; Durham Veteran's Affairs Health Care System, Durham, NC.
  • Khatri P; Center for Applied Genomics and Precision Medicine, Department of Medicine, Duke University, Durham, NC.
Crit Care Med ; 46(6): 915-925, 2018 06.
Article in En | MEDLINE | ID: mdl-29537985
ABSTRACT

OBJECTIVES:

To find and validate generalizable sepsis subtypes using data-driven clustering.

DESIGN:

We used advanced informatics techniques to pool data from 14 bacterial sepsis transcriptomic datasets from eight different countries (n = 700).

SETTING:

Retrospective analysis.

SUBJECTS:

Persons admitted to the hospital with bacterial sepsis.

INTERVENTIONS:

None. MEASUREMENTS AND MAIN

RESULTS:

A unified clustering analysis across 14 discovery datasets revealed three subtypes, which, based on functional analysis, we termed "Inflammopathic, Adaptive, and Coagulopathic." We then validated these subtypes in nine independent datasets from five different countries (n = 600). In both discovery and validation data, the Adaptive subtype is associated with a lower clinical severity and lower mortality rate, and the Coagulopathic subtype is associated with higher mortality and clinical coagulopathy. Further, these clusters are statistically associated with clusters derived by others in independent single sepsis cohorts.

CONCLUSIONS:

The three sepsis subtypes may represent a unifying framework for understanding the molecular heterogeneity of the sepsis syndrome. Further study could potentially enable a precision medicine approach of matching novel immunomodulatory therapies with septic patients most likely to benefit.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Sepsis / Gene Expression Profiling Type of study: Observational_studies Limits: Adolescent / Adult / Aged / Female / Humans / Male / Middle aged Language: En Journal: Crit Care Med Year: 2018 Type: Article Affiliation country: Canada

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Sepsis / Gene Expression Profiling Type of study: Observational_studies Limits: Adolescent / Adult / Aged / Female / Humans / Male / Middle aged Language: En Journal: Crit Care Med Year: 2018 Type: Article Affiliation country: Canada