Evidence map›Paper›PMID 39192974›Full record

ArticleFrontiers in immunology2024

Genomic insights into pediatric intestinal inflammatory and eosinophilic disorders using single-cell RNA-sequencing.

Marissa R Keever-Keigher, Lisa Harvey, Veronica Williams, Carrie A Vyhlidal, Atif A Ahmed, Jeffery J Johnston, Daniel A Louiselle, Elin Grundberg, Tomi Pastinen, Craig A Friesen and 3 more

Abstract read
In one paragraph

Article in Frontiers in immunology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Review
  2. Review
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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

13 authors.

Marissa R Keever-KeigherChildren's Mercy Kansas City, Kansas, MO, United States.
Lisa HarveyChildren's Mercy Kansas City, Kansas, MO, United States.
Veronica WilliamsNemours Children's Health, Jacksonville, FL, United States.
Carrie A VyhlidalKCAS Bioanalytical & Biomarker Services, Shawnee, KS, United States.
Atif A AhmedSeattle Children's Hospitals, University of Washington, Seattle, WA, United States.
Jeffery J JohnstonChildren's Mercy Kansas City, Kansas, MO, United States.
Daniel A LouiselleChildren's Mercy Kansas City, Kansas, MO, United States.
Elin GrundbergChildren's Mercy Kansas City, Kansas, MO, United States.
Tomi PastinenChildren's Mercy Kansas City, Kansas, MO, United States.
Craig A FriesenChildren's Mercy Kansas City, Kansas, MO, United States.
Rachel ChevalierChildren's Mercy Kansas City, Kansas, MO, United States.
Craig Smail *Children's Mercy Kansas City, Kansas, MO, United States.
Valentina Shakhnovich *Children's Mercy Kansas City, Kansas, MO, United States.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Chronic inflammation of the gastrointestinal tissues underlies gastrointestinal inflammatory disorders, leading to tissue damage and a constellation of painful and debilitating symptoms. These disorders include inflammatory bowel diseases (Crohn's disease and ulcerative colitis), and eosinophilic disorders (eosinophilic esophagitis and eosinophilic duodenitis). Gastrointestinal inflammatory disorders can often present with overlapping symptoms necessitating the use of invasive procedures to give an accurate diagnosis. Methods: This study used peripheral blood mononuclear cells from individuals with Crohn's disease, ulcerative colitis, eosinophilic esophagitis, and eosinophilic duodenitis to better understand the alterations to the transcriptome of individuals with these diseases and identify potential markers of active inflammation within the peripheral blood of patients that may be useful in diagnosis. Single-cell RNA-sequencing was performed on peripheral blood mononuclear cells isolated from the blood samples of pediatric patients diagnosed with gastrointestinal disorders, including Crohn's disease, ulcerative colitis, eosinophilic esophagitis, eosinophilic duodenitis, and controls with histologically healthy gastrointestinal tracts. Results: We identified 730 (FDR < 0.05) differentially expressed genes between individuals with gastrointestinal disorders and controls across eight immune cell types. Discussion: There were common patterns among GI disorders, such as the widespread upregulation of

Indexed as

EosinophiliaSingle-Cell AnalysisAdolescentBiomarkersChildChild, PreschoolColitis, UlcerativeCrohn DiseaseEnteritisEosinophilic EsophagitisFemaleGastritisGene Expression ProfilingGenomicsHumansLeukocytes, MononuclearBiomarkersgastrointestinal disordergenomicspediatricsRNA-seqsingle-cell

Identifiers

PMID39192974
PMCPMC11347318

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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.