Evidence map›Paper›PMID 36140740›Full record

ArticleGenes2022

Unexpected Actors in Inflammatory Bowel Disease Revealed by Machine Learning from Whole-Blood Transcriptomic Data.

Jan K Nowak, Cyntia J Szymańska, Aleksandra Glapa-Nowak, Rémi Duclaux-Loras, Emilia Dybska, Jerzy Ostrowski, Jarosław Walkowiak, Alex T Adams

Open access · goldAbstract read
In one paragraph

Article in Genes, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.3field-weighted citation impact, top 18% 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, 7 citations in OpenAlex.

  1. Article
  2. Review
  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

8 authors at 4 institutions in 3 countries.

Jan K NowakDepartment of Pediatric Gastroenterology and Metabolic Diseases, Poznan University of Medical Sciences, 60572 Poznan, Poland.ORCID 0000-0003-0953-2188
Cyntia J SzymańskaDepartment of Pediatric Gastroenterology and Metabolic Diseases, Poznan University of Medical Sciences, 60572 Poznan, Poland.
Aleksandra Glapa-NowakDepartment of Pediatric Gastroenterology and Metabolic Diseases, Poznan University of Medical Sciences, 60572 Poznan, Poland.ORCID 0000-0002-3017-0524
Rémi Duclaux-LorasINSERM U1111, Centre International de Recherche en Infectiologie, Université Claude Bernard Lyon 1, 69364 Lyon, France.
Emilia DybskaDepartment of Pediatric Gastroenterology and Metabolic Diseases, Poznan University of Medical Sciences, 60572 Poznan, Poland.ORCID 0000-0003-2692-2487
Jerzy OstrowskiDepartment of Genetics, Maria Skłodowska-Curie National Research Institute of Oncology, 02781 Warsaw, Poland.
Jarosław WalkowiakDepartment of Pediatric Gastroenterology and Metabolic Diseases, Poznan University of Medical Sciences, 60572 Poznan, Poland.ORCID 0000-0001-5813-5707
Alex T AdamsTranslational Gastroenterology Unit, Nuffield Department of Medicine, Experimental Medicine Division, University of Oxford, John Radcliffe Hospital, Oxford OX3 9DU, UK.
Poznan University of Medical Sciences · PLJohn Radcliffe Hospital · GBPostgraduate School of Molecular Medicine · PLUniversité Claude Bernard Lyon 1 · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Although big data from transcriptomic analyses have helped transform our understanding of inflammatory bowel disease (IBD), they remain underexploited. We hypothesized that the application of machine learning using lasso regression to transcriptomic data from IBD patients and controls can help identify previously overlooked genes. Transcriptomic data provided by Ostrowski et al. (ENA PRJEB28822) were subjected to a two-stage process of feature selection to discriminate between IBD and controls. First, a principal component analysis was used for dimensionality reduction. Second, the least absolute shrinkage and selection operator (lasso) regression was employed to identify genes potentially involved in the pathobiology of IBD. The study included data from 294 participants: 100 with ulcerative colitis (48 adults and 52 children), 99 with Crohn's disease (45 adults and 54 children), and 95 controls (46 adults and 49 children). IBD patients presented a wide range of disease severity. Lasso regression preceded by principal component analysis successfully selected interesting features in the IBD transcriptomic data and yielded 12 models. The models achieved high discriminatory value (range of the area under the receiver operating characteristic curve 0.61-0.95) and identified over 100 genes as potentially associated with IBD.

Indexed as

Colitis, UlcerativeInflammatory Bowel DiseasesAdultChildHumansMachine LearningTranscriptomeTransforming Growth Factor betaTransforming Growth Factor betaCrohn’s diseaseexpressioninflammatory bowel diseaseTGF-betaulcerative colitis

Identifiers

PMID36140740
PMCPMC9498489
OpenAlexW4294151360

What OpenQuestion holds

Textmetadata
LicenceCC BY
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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.