Evidence map›Paper›PMID 23884467›Full record

ArticleScience translational medicine2013

An integrated clinico-metabolomic model improves prediction of death in sepsis.

Raymond J Langley, Ephraim L Tsalik, Jennifer C van Velkinburgh, Seth W Glickman, Brandon J Rice, Chunping Wang, Bo Chen, Lawrence Carin, Arturo Suarez, Robert P Mohney and 28 more

Abstract read
In one paragraph

Article in Science translational medicine, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 296 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
296citing papers in PubMed, 2 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

296 citing papers in PubMed, 2 syntheses or guidelines pooled it.

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  5. A Multi-Omic Mosaic Model of Acetaminophen Induced Alanine Aminotransferase Elevation.Journal of medical toxicology : official journal of the American College of Medical Toxicology · 2023
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236 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

38 authors.

Raymond J LangleyNational Center for Genome Resources, Santa Fe, NM 87505, USA.
Ephraim L Tsalik
Jennifer C van Velkinburgh
Seth W Glickman
Brandon J Rice
Chunping Wang
Bo Chen
Lawrence Carin
Arturo Suarez
Robert P Mohney
Debra H Freeman
Mu Wang
Jinsam You
Jacob Wulff
J Will Thompson
M Arthur Moseley
Stephanie Reisinger
Brian T Edmonds
Brian Grinnell
David R Nelson
Darrell L Dinwiddie
Neil A Miller
Carol J Saunders
Sarah S Soden
Angela J Rogers
Lee Gazourian
Laura E Fredenburgh
Anthony F Massaro
Rebecca M Baron
Augustine M K Choi
G Ralph Corey
Geoffrey S Ginsburg
Charles B Cairns
Ronny M Otero
Vance G Fowler
Emanuel P Rivers
Christopher W Woods
Stephen F Kingsmore

Funding

ZUNI HEALTH INITIATIVE-PILOT STUDYP20RR016480 · NCRR · NEW MEXICO STATE UNIVERSITY LAS CRUCES · PI ZHANG, PENG F · 2001 to 2011
$33.7M
Mesenchymal Stromal Cell Conditioning by Carbon MonoxideP01HL108801 · NHLBI · BRIGHAM AND WOMEN'S HOSPITAL · PI CHOI, AUGUSTINE M · 2011 to 2015
$13.8M
The Role of HEME Oxygenase in Hyperoxic Lung InjuryR01HL055330 · NHLBI · YALE UNIVERSITY · PI CHOI, AUGUSTINE M, CHOI, MARY E · 1998 to 2021
$6.6M
ConProject-001U19HD077693 · NICHD · RADY PEDIATRIC GENOMICS & SYSTEMS MEDICINE INSTITUTE · PI KINGSMORE, STEPHEN FRANCIS · 2013 to 2018
$6.2M
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
Heme oxygenase-1: Regulation and Function in CaveolaeR01HL079904 · NHLBI · WEILL MEDICAL COLL OF CORNELL UNIV · PI CHOI, MARY E · 2005 to 2014
$2.9M
The Inflammasome: A Novel Biomarker in ALI/ARDSR01HL112747 · NHLBI · BRIGHAM AND WOMEN'S HOSPITAL · PI BARON, REBECCA M · 2012 to 2015
$1.8M
NCRR NIH HHS P20 RR016480NCRR NIH HHS P20RR016480NHLBI NIH HHS HL05530NHLBI NIH HHS HL112747NHLBI NIH HHS P01 HL108801NHLBI NIH HHS R01 HL055330NHLBI NIH HHS R01 HL079904NHLBI NIH HHS R01 HL112747NIAID NIH HHS U01 AI066569NIAID NIH HHS U01AI066569NICHD NIH HHS U19 HD077693PHS HHS HHSN266200400064C
6 · The paper itself

Abstract

Sepsis is a common cause of death, but outcomes in individual patients are difficult to predict. Elucidating the molecular processes that differ between sepsis patients who survive and those who die may permit more appropriate treatments to be deployed. We examined the clinical features and the plasma metabolome and proteome of patients with and without community-acquired sepsis, upon their arrival at hospital emergency departments and 24 hours later. The metabolomes and proteomes of patients at hospital admittance who would ultimately die differed markedly from those of patients who would survive. The different profiles of proteins and metabolites clustered into the following groups: fatty acid transport and β-oxidation, gluconeogenesis, and the citric acid cycle. They differed consistently among several sets of patients, and diverged more as death approached. In contrast, the metabolomes and proteomes of surviving patients with mild sepsis did not differ from survivors with severe sepsis or septic shock. An algorithm derived from clinical features together with measurements of five metabolites predicted patient survival. This algorithm may help to guide the treatment of individual patients with sepsis.

Indexed as

Models, TheoreticalAgedAlgorithmsFemaleHumansMaleMetabolomicsMiddle AgedProteomicsSepsis

Identifiers

PMID23884467
PMCPMC3924586

What OpenQuestion holds

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LicenceTDM
Read underepoch 390

Registered trials

None linked

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.