Evidence map›Paper›PMID 26217105›Full record

ArticleGenomics insights2012

Transcriptional Changes of Blood Eosinophils After Methacholine Inhalation Challenge in Asthmatics.

Scott J Tebbutt, Jian-Qing He, Amrit Singh, Casey P Shannon, Jian Ruan, Chris Carlsten

Open access · bronzeAbstract read
In one paragraph

Article in Genomics insights, 2012. 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
0.3field-weighted citation impact, top 38% 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

3 citing papers in PubMed, 4 citations in OpenAlex.

  1. CCR3 deficiency shifts adaptive to innate-driven immunity in asthma.The journal of allergy and clinical immunology. Global · 2025
    Article
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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

6 authors at 2 institutions in 1 country.

Scott J TebbuttJames Hogg Research Centre, St. Paul's Hospital, University of British Columbia, Vancouver, British Columbia, Canada. ; Institute for HEART+LUNG Health, Vancouver, BC, Canada. ; Department of Medicine, Division of Respiratory Medicine, University of British Columbia, Vancouver, BC, Canada.
Jian-Qing HeJames Hogg Research Centre, St. Paul's Hospital, University of British Columbia, Vancouver, British Columbia, Canada. ; Institute for HEART+LUNG Health, Vancouver, BC, Canada.
Amrit SinghJames Hogg Research Centre, St. Paul's Hospital, University of British Columbia, Vancouver, British Columbia, Canada. ; Institute for HEART+LUNG Health, Vancouver, BC, Canada.
Casey P ShannonJames Hogg Research Centre, St. Paul's Hospital, University of British Columbia, Vancouver, British Columbia, Canada. ; Institute for HEART+LUNG Health, Vancouver, BC, Canada.
Jian RuanJames Hogg Research Centre, St. Paul's Hospital, University of British Columbia, Vancouver, British Columbia, Canada. ; Institute for HEART+LUNG Health, Vancouver, BC, Canada.
Chris CarlstenInstitute for HEART+LUNG Health, Vancouver, BC, Canada. ; Department of Medicine, Division of Respiratory Medicine, University of British Columbia, Vancouver, BC, Canada. ; Vancouver Coastal Health Research Institute, Vancouver General Hospital, Vancouver, BC, Canada.
University of British Columbia · CAVancouver Coastal Health Research Institute · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMethacholine challenge is commonly used within the asthma diagnostic algorithm. Methacholine challenge has recently been shown to induce airway remodelling in asthma via bronchoconstriction, without additional airway inflammation. We evaluated the effect of methacholine-induced bronchoconstriction on the peripheral whole-blood transcriptome.

methodsFourteen males with adult-onset, occupational asthma, 26-77 years of age, underwent methacholine inhalation challenges. The concentration of methacholine eliciting a ≥20% fall in FEV1 (PC20) was determined. Blood was collected immediately prior to and two hours after challenge. Complete blood counts and leukocyte differentials were obtained. Transcriptome analysis was performed using Affymetrix GeneChip(®) Human Gene 1.0 ST arrays. Data were analyzed using robust LIMMA and SAM. The cell-specific Significance Analysis of Microarrays (csSAM) algorithm was used to deconvolute the gene expression data according to cell type.

resultsMicroarray pathway analysis indicated that inflammatory processes were differentially affected. CsSAM identified 1,559 transcripts differentially expressed (all down-regulated) between pre- and post-methacholine in eosinophils at a false discovery cutoff of 10%. Notable changes included the GOLGA5 and METTL2B genes and the protein ubiquitination and CCR3 pathways.

conclusionsWe demonstrated significant changes in the peripheral blood eosinophil-specific transcriptome of asthmatics two hours after methacholine challenge. CCR3 and protein ubiquitination pathways are both significantly down-regulated.

Indexed as

asthmaCCR3gene expressionmicroarrayperipheral bloodprotein ubiquitination

Identifiers

PMID26217105
PMCPMC4510604
OpenAlexW2024545478

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.