Evidence map›Paper›PMID 33374697›Full record

ArticleJournal of personalized medicine2020

A 33-mRNA Classifier Is Able to Produce Inflammopathic, Adaptive, and Coagulopathic Endotypes with Prognostic Significance: The Outcomes of Metabolic Resuscitation Using Ascorbic Acid, Thiamine, and Glucocorticoids in the Early Treatment of Sepsis (ORANGES) Trial.

Jose Iglesias, Andrew V Vassallo, Oliver Liesenfeld, Jerrold S Levine, Vishal V Patel, Jesse B Sullivan, Joseph B Cavanaugh, Yasmine Elbaga, Timothy E Sweeney

Open access · goldAbstract read
In one paragraph

Article in Journal of personalized medicine, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
2.2field-weighted citation impact, top 13% of its field
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

12 citing papers in PubMed, 21 citations in OpenAlex.

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  10. Sepsis as a Challenge for Personalized Medicine.Journal of personalized medicine · 2022
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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

9 authors at 4 institutions in 1 country.

Jose IglesiasDepartment of Critical Care, Department of Nephrology, Community Medical Center, Toms River, NJ 08755, USA.ORCID 0000-0001-7851-0498
Andrew V VassalloDepartment of Pharmacy, Community Medical Center, Toms River, NJ 08755, USA.
Oliver LiesenfeldInflammatix, Inc., Burlingame, CA 94010, USA.ORCID 0000-0002-4348-5509
Jerrold S LevineDepartment of Medicine Section of Nephrology, University of Illinois at Chicago, Chicago, IL 60612, USA.
Vishal V PatelDepartment of Pharmacy, Community Medical Center, Toms River, NJ 08755, USA.ORCID 0000-0002-0886-5063
Jesse B SullivanSchool of Pharmacy & Health Sciences, Fairleigh Dickinson University, Florham Park, NJ 07932, USA.
Joseph B CavanaughDepartment of Pharmacy, Community Medical Center, Toms River, NJ 08755, USA.
Yasmine ElbagaDepartment of Pharmacy, Monmouth Medical Center Southern Campus, Lakewood, NJ 08701, USA.
Timothy E SweeneyInflammatix, Inc., Burlingame, CA 94010, USA.ORCID 0000-0002-3596-1093
Community Medical Center · USFairleigh Dickinson University · USMonmouth Medical Center · USUniversity of Illinois Chicago · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundRetrospective analysis of the transcriptomic host response in sepsis has demonstrated that sepsis can be separated into three endotypes-inflammatory (IE), adaptive (AE), and coagulopathic (CE), which have demonstrated prognostic significance. We undertook a prospective transcriptomic host response analysis in a subgroup of patients enrolled in the Outcomes of Metabolic Resuscitation Using Ascorbic Acid, Thiamine, and Glucocorticoids in the Early Treatment of Sepsis (ORANGES) trial.

methodsBlood was obtained from 51 patients and profiled using a pre-established 33-mRNA classifier to determine sepsis endotypes. Endotypes were compared to therapy subgroups and clinical outcomes.

resultsWe redemonstrated a statistically significant difference in mortality between IE, AE, and CE patients, with CE patients demonstrating the highest mortality (40%), and AE patients the lowest mortality (5%,

conclusionThis subset of patients from the ORANGES trial confirmed previous retrospective findings that a 33-mRNA classifier can group patients into IE, AE, and CE endotypes having prognostic significance. A novel finding of this study identifying an association between endotype and corticosteroid therapy warrants further study in support of future diagnostic use of the endotyping classifier.

Indexed as

ascorbic acidcoagulopathicendotypingHAT therapyhydrocortisonesepsisseptic shockthiaminevitamin c

Identifiers

PMID33374697
PMCPMC7822486
OpenAlexW3115428705

What OpenQuestion holds

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Registered trials

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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.