Evidence map›Paper›PMID 32170472›Full record

ArticleMetabolomics : Official journal of the Metabolomic Society2020

New markers for sepsis caused by Pseudomonas aeruginosa during burn infection.

Moamen M Elmassry, Nithya S Mudaliar, Jane A Colmer-Hamood, Michael J San Francisco, John A Griswold, Sharmila Dissanaike, Abdul N Hamood

Open access · bronzeAbstract read
In one paragraph

Article in Metabolomics : Official journal of the Metabolomic Society, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed, 1 pooled it
1.8field-weighted citation impact, top 15% 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

24 citing papers in PubMed, 1 synthesis or guideline pooled it, 34 citations in OpenAlex.

  1. Pooled it
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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

7 authors at 1 institution in 1 country.

Moamen M ElmassryDepartment of Biological Sciences, Texas Tech University, Lubbock, TX, USA.ORCID 0000-0002-1193-7822
Nithya S MudaliarDepartment of Surgery, Texas Tech University Health Sciences Center, Lubbock, TX, USA.
Jane A Colmer-HamoodDepartment of Immunology and Molecular Microbiology, Texas Tech University Health Sciences Center, 3601 4th Street STOP 6591, Lubbock, TX, 79430-6591, USA.ORCID 0000-0002-3768-5168
Michael J San FranciscoDepartment of Biological Sciences, Texas Tech University, Lubbock, TX, USA.ORCID 0000-0002-1321-8522
John A GriswoldDepartment of Surgery, Texas Tech University Health Sciences Center, Lubbock, TX, USA.
Sharmila DissanaikeDepartment of Surgery, Texas Tech University Health Sciences Center, Lubbock, TX, USA.
Abdul N HamoodDepartment of Surgery, Texas Tech University Health Sciences Center, Lubbock, TX, USA. abdul.hamood@ttuhsc.edu.ORCID 0000-0001-7193-7827
Texas Tech University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionSepsis is a leading cause of mortality in burn patients. One of the major causes of sepsis in burn patients is Pseudomonas aeruginosa. We hypothesized that during dissemination from infected burn wounds and subsequent sepsis, P. aeruginosa affects the metabolome of the blood resulting in changes to specific metabolites that would serve as biomarkers for early diagnosis of sepsis caused by P. aeruginosa.

objectivesTo identify specific biomarkers in the blood after sepsis caused by P. aeruginosa infection of burns.

methodsGas chromatography with time-of-flight mass spectrometry was used to compare the serum metabolome of mice that were thermally injured and infected with P. aeruginosa (B-I) to that of mice that were neither injured nor infected, mice that were injured but not infected, and mice that were infected but not injured.

resultsSerum levels of 19 metabolites were significantly increased in the B-I group compared to controls while levels of eight metabolites were significantly decreased. Thymidine, thymine, uridine, and uracil (related to pyrimidine metabolism), malate and succinate (a possible sign of imbalance in the tricarboxylic acid cycle), 5-oxoproline (related to glutamine and glutathione metabolism), and trans-4-hydroxyproline (a major component of the protein collagen) were increased. Products of amino acid metabolism were significantly decreased in the B-I group, including methionine, tyrosine, indole-3-acetate, and indole-3-propionate.

conclusionIn all, 26 metabolites were identified, including a unique combination of five metabolites (trans-4-hydroxyproline, 5-oxoproline, glycerol-3-galactoside, indole-3-acetate, and indole-3-propionate) that could serve as a set of biomarkers for early diagnosis of sepsis caused by P. aeruginosa in burn patients.

Indexed as

AnimalsBiomarkersBurnsChromatography, GasDisease Models, AnimalFemaleMass SpectrometryMetabolomicsMicePseudomonas aeruginosaSepsisWound InfectionBiomarkersBurnGas chromatography with time-of-flight mass spectrometryInfectionMetabolomicsPseudomonas aeruginosaSepsis

Identifiers

PMID32170472
PMCPMC7223005
OpenAlexW3012514325

What OpenQuestion holds

Textmetadata
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.