Evidence map›Paper›PMID 31583479›Full record

ArticleMetabolomics : Official journal of the Metabolomic Society2019

In vitro profiling of endothelial volatile organic compounds under resting and pro-inflammatory conditions.

V Longo, A Forleo, S Capone, E Scoditti, M A Carluccio, P Siciliano, M Massaro

Abstract read
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In one paragraph

Article in Metabolomics : Official journal of the Metabolomic Society, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed, 1 pooled it
0.4field-weighted citation impact, top 40% 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

4 citing papers in PubMed, 1 synthesis or guideline pooled it, 11 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Article
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 2 institutions in 1 country.

V LongoNational Research Council of Italy, Institute for Microelectronics and Microsystems, Lecce, Italy. valentina.longo@le.imm.cnr.it.ORCID 0000-0002-5763-8879
A ForleoNational Research Council of Italy, Institute for Microelectronics and Microsystems, Lecce, Italy.ORCID 0000-0003-2291-8675
S CaponeNational Research Council of Italy, Institute for Microelectronics and Microsystems, Lecce, Italy.ORCID 0000-0001-6448-9261
E ScodittiNational Research Council of Italy, Institute of Clinical Physiology, Lecce, Italy.ORCID 0000-0003-2753-8487
M A CarluccioNational Research Council of Italy, Institute of Clinical Physiology, Lecce, Italy.ORCID 0000-0002-8307-1829
P SicilianoNational Research Council of Italy, Institute for Microelectronics and Microsystems, Lecce, Italy.ORCID 0000-0001-9748-0925
M MassaroNational Research Council of Italy, Institute of Clinical Physiology, Lecce, Italy. marika.massaro@ifc.cnr.it.ORCID 0000-0001-6124-5077
National Research Council · ITIstituto di Fisiologia Clinica · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionThe evaluation of volatile organic compounds(VOCs) emitted by human body offers a unique tool to set up new non-invasive devices for early diagnosis and long-lasting monitoring of most human diseases. However, their cellular origin and metabolic fate have not been completely elucidated yet, thus limiting their clinical application. Endothelium acts as an interface between blood and surrounding tissues. As such, it adapts its physiology in response to different environmental modifications thus playing a role in the pathogenesis of many metabolic and inflammatory diseases.

objectivesSince endothelium specifically reshapes its physiologic functions upon environmental changes the objective of this study was to evaluate if and how pro-inflammatory stimuli affect VOC metabolism in endothelial cell in culture.

methodsGas chromatography with mass spectrometric detection was applied to profile VOCs in the headspace of cultured endothelial cells (EC) in the absence or presence of the pro-inflammatory stimulus lipopolysaccharide (LPS).

resultsWe observed that, under resting conditions, EC affected the amount of 58 VOCs belonging to aldehyde, alkane and ketone families. Among these, LPS significantly altered the amount of 15 VOCs. ROC curves show a perfect performance (AUC = 1) for 10 metabolites including 1-butanol, 3-methyl-1-butanol and 2-ethyl-1-hexanol. DISCUSSION: The emission and uptake of the aforementioned VOCs disclose potential unexplored metabolic pathways for EC that deserve to be investigated. Overall, we identified new candidate VOC potentially exploitable, upon experimental confirm in in vivo model of disease, as potential biomarkers of sepsis and pro-inflammatory clinical settings.

Indexed as

Adaptation, PhysiologicalBiomarkersEndotheliumHumansLipopolysaccharidesMetabolomicsUmbilical VeinsVolatile Organic CompoundsBiomarkersLipopolysaccharidesVolatile Organic CompoundsBiomarkersEndothelial cellsGC–MSInflammationSepsisVOCsVolatile organic compounds

Identifiers

PMID31583479
OpenAlexW2977824644

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.