Evidence map›Paper›PMID 29537985›Full record

ArticleCritical care medicine2018

Unsupervised Analysis of Transcriptomics in Bacterial Sepsis Across Multiple Datasets Reveals Three Robust Clusters.

Timothy E Sweeney, Tej D Azad, Michele Donato, Winston A Haynes, Thanneer M Perumal, Ricardo Henao, Jesús F Bermejo-Martin, Raquel Almansa, Eduardo Tamayo, Judith A Howrylak and 13 more

Abstract read
In one paragraph

Article in Critical care medicine, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 209 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
209citing papers in PubMed, 3 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

209 citing papers in PubMed, 3 syntheses or guidelines pooled it.

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149 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

23 authors.

Timothy E SweeneyStanford Institute for Immunity, Transplantation and Infection, Stanford University School of Medicine, Stanford, CA.
Tej D AzadStanford Institute for Immunity, Transplantation and Infection, Stanford University School of Medicine, Stanford, CA.
Michele DonatoStanford Institute for Immunity, Transplantation and Infection, Stanford University School of Medicine, Stanford, CA.
Winston A HaynesStanford Institute for Immunity, Transplantation and Infection, Stanford University School of Medicine, Stanford, CA.
Thanneer M PerumalSage Bionetworks, Seattle, WA.
Ricardo HenaoCenter for Applied Genomics and Precision Medicine, Department of Medicine, Duke University, Durham, NC.
Jesús F Bermejo-MartinBio Sepsis, Hospital Clínico Universitario de Valladolid/IECSCYL, Valladolid, Spain.
Raquel AlmansaBio Sepsis, Hospital Clínico Universitario de Valladolid/IECSCYL, Valladolid, Spain.
Eduardo TamayoBio Sepsis, Hospital Clínico Universitario de Valladolid/IECSCYL, Valladolid, Spain.
Judith A HowrylakDivision of Pulmonary, Allergy, and Critical Care Medicine, Department of Medicine, Penn State Milton S. Hershey Medical Center, Hershey, PA.
Augustine ChoiDepartment of Medicine, Cornell Medical Center, New York, NY.
Grant P ParnellCentre for Immunology and Allergy Research, Westmead Institute for Medical Research, Sydney, NSW, Australia.
Benjamin Tang
Marshall NicholsCenter for Applied Genomics and Precision Medicine, Department of Medicine, Duke University, Durham, NC.
Christopher W WoodsCenter for Applied Genomics and Precision Medicine, Department of Medicine, Duke University, Durham, NC.
Geoffrey S GinsburgCenter for Applied Genomics and Precision Medicine, Department of Medicine, Duke University, Durham, NC.
Stephen F KingsmoreRady Children's Institute for Genomic Medicine, San Diego, CA.
Larsson OmbergSage Bionetworks, Seattle, WA.
Lara M MangraviteSage Bionetworks, Seattle, WA.
Hector R WongDivision of Critical Care Medicine, Cincinnati Children's Hospital Medical Center and Cincinnati Children's Research Foundation, Cincinnati, OH.
Ephraim L TsalikCenter for Applied Genomics and Precision Medicine, Department of Medicine, Duke University, Durham, NC.
Raymond J LangleyDepartment of Pharmacology, University of South Alabama, Mobile, AL.
Purvesh KhatriStanford Institute for Immunity, Transplantation and Infection, Stanford University School of Medicine, Stanford, CA.

Funding

Using a tonsil organoid system to probe conditions for the induction of protective antibody and T cell responses to influenza.U19AI057229 · NIAID · STANFORD UNIVERSITY · PI Mark Morris Davis · 2003 to 2026
$88.5M
ZUNI HEALTH INITIATIVE-PILOT STUDYP20RR016480 · NCRR · NEW MEXICO STATE UNIVERSITY LAS CRUCES · PI ZHANG, PENG F · 2001 to 2011
$33.7M
UAB Center for Clinical and Translational Science (CCTS)UL1TR001417 · NCATS · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI KIMBERLY, ROBERT P. · 2015 to 2018
$31.4M
Translational Incubator CoreU19AI109662 · NIAID · STANFORD UNIVERSITY · PI GLENN, JEFFREY S · 2014 to 2019
$28.6M
POSTDOCTORAL TRAINING IN MEDICAL INFORMATION SCIENCEST15LM007033 · NLM · STANFORD UNIVERSITY · PI SYLVIA KATINA PLEVRITIS · 1985 to 2026
$25.5M
Penn State Clinical and Translational Science InstituteUL1TR000127 · NCATS · PENNSYLVANIA STATE UNIV HERSHEY MED CTR · PI SINOWAY, LAWRENCE I · 2012 to 2015
$17.1M
TrainingU54AI117925 · NIAID · STANFORD UNIVERSITY · PI MUSEN, MARK A · 2014 to 2018
$12.9M
Penn State Clinical and Translational Science InstituteKL2TR000126 · NCATS · PENNSYLVANIA STATE UNIV HERSHEY MED CTR · PI SINOWAY, LAWRENCE I · 2012 to 2015
$3.2M
Plasma Protein Biomarker-Based Diagnostics Of Outcome In Sepsis and CAPU01AI066569 · NIAID · NATIONAL CENTER FOR GENOME RESOURCES · PI KINGSMORE, STEPHEN FRANCIS · 2005 to 2010
$2.9M
Novel diagnostic and stratification tools for septic shockR01GM108025 · NIGMS · CINCINNATI CHILDRENS HOSP MED CTR · PI WONG, HECTOR R. · 2014 to 2017
$2.3M
Stratification of pediatric septic shockR01GM099773 · NIGMS · CINCINNATI CHILDRENS HOSP MED CTR · PI WONG, HECTOR R. · 2012 to 2015
$1.5M
NCATS NIH HHS KL2 TR000126NCATS NIH HHS UL1 TR000127NCATS NIH HHS UL1 TR001417NCRR NIH HHS P20 RR016480NIAID NIH HHS U01 AI066569NIAID NIH HHS U19 AI057229NIAID NIH HHS U19 AI109662NIAID NIH HHS U54 AI117925NIGMS NIH HHS R01 GM099773NIGMS NIH HHS R01 GM108025NLM NIH HHS T15 LM007033
6 · The paper itself

Abstract

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

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

settingRetrospective analysis. SUBJECTS: Persons admitted to the hospital with bacterial sepsis.

interventionsNone. MEASUREMENTS AND MAIN

resultsA 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.

conclusionsThe 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.

Indexed as

Gene Expression ProfilingAdaptive ImmunityAdolescentAdultAgedBlood Coagulation DisordersCluster AnalysisDatasets as TopicFemaleHumansImmunity, InnateInflammationMaleMiddle AgedRetrospective StudiesSepsis

Identifiers

PMID29537985
PMCPMC5953807

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.