Evidence map›Paper›PMID 37233766›Full record

ArticleAnalytical and bioanalytical chemistry2023

Application of untargeted volatile profiling in inflammatory bowel disease research.

Natalia Arroyo-Manzanares, María García-Nicolás, Fuensanta Abellán-Alfocea, Laura Prieto-Baeza, Natalia Campillo, Blanca Del Val Oliver, José Zarauz-García, Luis Sáenz, Pilar Viñas

Abstract read
In one paragraph

Article in Analytical and bioanalytical chemistry, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

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

2 citing papers in PubMed.

  1. Article
  2. Review
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.

Natalia Arroyo-ManzanaresDepartment of Analytical Chemistry, Faculty of Chemistry, University of Murcia, Regional Campus of International Excellence "Campus Mare Nostrum", E-30100, Murcia, Spain.
María García-NicolásDepartment of Analytical Chemistry, Faculty of Chemistry, University of Murcia, Regional Campus of International Excellence "Campus Mare Nostrum", E-30100, Murcia, Spain.
Fuensanta Abellán-AlfoceaDepartment of Analytical Chemistry, Faculty of Chemistry, University of Murcia, Regional Campus of International Excellence "Campus Mare Nostrum", E-30100, Murcia, Spain.
Laura Prieto-BaezaDepartment of Analytical Chemistry, Faculty of Chemistry, University of Murcia, Regional Campus of International Excellence "Campus Mare Nostrum", E-30100, Murcia, Spain.
Natalia CampilloDepartment of Analytical Chemistry, Faculty of Chemistry, University of Murcia, Regional Campus of International Excellence "Campus Mare Nostrum", E-30100, Murcia, Spain.
Blanca Del Val OliverInternal Medicine Service - Gastroenterology and Hepatology Section, Hospital General Universitario Rafael Méndez, Lorca, Spain.
José Zarauz-GarcíaLaboratory Medicine Department, Hospital General Universitario Rafael Méndez, Lorca, Spain.
Luis SáenzLaboratory Medicine Department, Hospital General Universitario Rafael Méndez, Lorca, Spain.
Pilar ViñasDepartment of Analytical Chemistry, Faculty of Chemistry, University of Murcia, Regional Campus of International Excellence "Campus Mare Nostrum", E-30100, Murcia, Spain. pilarvir@um.es.ORCID http://orcid.org/0000-0001-5219-3711

Funding

Ministerio de Ciencia e Innovación PID2021-123201NB-I00
6 · The paper itself

Abstract

Inflammatory bowel disease (IBD) diagnosis depends on criteria based on histological, endoscopic, radiological, and clinical results. These studies show drawbacks as being expensive, invasive, and time-consuming. In this work, an untargeted metabolomic strategy based on the monitoring of volatile compounds in serum by headspace gas chromatography-mass spectrometry is proposed as a complementary, fast, and efficient test for IBD patient diagnosis. To develop the method and build a chemometric model that allows the IBD diagnosis, serum samples including IBD patients and healthy volunteers were collected. Analyses were performed by incubating 400 µL of serum for 10 min at 90 °C. For data processing, an untargeted metabolomic strategy was used. A total of 96 features were detected, of which a total of 10 volatile compounds could be identified and confirmed by means of the analysis of real standards. The chemometric treatment consisted of a discriminant analysis of orthogonal partial least squares (OPLS-DA) obtaining a 100% of classification rate, since all the analyzed samples were correctly classified.

Indexed as

Inflammatory Bowel DiseasesVolatile Organic CompoundsDiscriminant AnalysisGas Chromatography-Mass SpectrometryHumansLeast-Squares AnalysisMetabolomicsVolatile Organic CompoundsChemometricsGas chromatography–mass spectrometryHeadspaceInflammatory bowel diseaseUntargeted metabolomic strategy

Identifiers

PMID37233766
PMCPMC10289974

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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.