Evidence map›Paper›PMID 29883053›Full record

ArticleInternational forum of allergy & rhinology2018

Mucus T helper 2 biomarkers predict chronic rhinosinusitis disease severity and prior surgical intervention.

Justin H Turner, Ping Li, Rakesh K Chandra

Open access · greenAbstract read
In one paragraph

Article in International forum of allergy & rhinology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
3.9field-weighted citation impact, top 6% 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

26 citing papers in PubMed, 49 citations in OpenAlex.

  1. Article
  2. Establishing the PMThe Journal of allergy and clinical immunology · 2026
    Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Observational
  8. Article
  9. Article
  10. Article
  11. Inflammatory characteristics of central compartment atopic disease.International forum of allergy & rhinology · 2023
    Article
  12. Review
  13. Article
  14. Review
  15. [Research progress of biomarkers in nasal secretions in endotypes diagnosis and clinical application of chronic rhinosinusitis].Lin chuang er bi yan hou tou jing wai ke za zhi = Journal of clinical otorhinolaryngology head and neck surgery · 2022
    Review
  16. Article
  17. Review
  18. Review
  19. Inflammatory heterogeneity in aspirin-exacerbated respiratory disease.The Journal of allergy and clinical immunology · 2021
    Article
  20. 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

3 authors at 1 institution in 1 country.

Justin H TurnerDepartment of Otolaryngology-Head and Neck Surgery, Vanderbilt University School of Medicine, Nashville, TN.
Ping LiDepartment of Otolaryngology-Head and Neck Surgery, Vanderbilt University School of Medicine, Nashville, TN.
Rakesh K ChandraDepartment of Otolaryngology-Head and Neck Surgery, Vanderbilt University School of Medicine, Nashville, TN.
Vanderbilt University · US

Funding

The Vanderbilt Institute for Clinical and Translational Research (VICTR)UL1TR000445 · NCATS · VANDERBILT UNIVERSITY MEDICAL CENTER · PI BERNARD, GORDON RAPHAEL · 2012 to 2016
$41.4M
The Mechanism of Inflammation-mediated Olfactory Dysfunction in Chronic RhinosinusitisR03DC014809 · NIDCD · VANDERBILT UNIVERSITY MEDICAL CENTER · PI TURNER, JUSTIN H · 2015 to 2017
$473k
NCATS NIH HHS UL1 TR000445NIAID NIH HHS L30 AI113795NIDCD NIH HHS R03 DC014809
6 · The paper itself

Abstract

backgroundChronic rhinosinusitis (CRS) is a diverse clinical syndrome with a heterogeneous pathophysiology. Early attempts to identify CRS endotypes and biomarkers have largely relied on analysis of surgically obtained tissue, thus limiting their practical utility. This study examined the ability of mucus T helper 2 (Th2) biomarkers to predict CRS disease severity and clinical characteristics.

methodsCRS (n = 90) and healthy control subjects (n = 17) were prospectively enrolled prior to surgical intervention and mucus levels of interleukin (IL)-4, IL-5, and IL-13 were determined using a multiplex cytometric bead assay. Data for relevant cytokines was then scaled, normalized, and later combined to develop standardized metrics indicative of Th2-associated inflammation. Th2-high and Th2-low subgroups were consequently identified and validated against factors associated with disease severity and clinical outcomes.

resultsMucus levels of IL-5 and IL-13 were elevated in CRS subjects compared to controls, while no significant difference was noted for IL-4. IL-5 and IL-13 high CRS were associated with worse objective measures of disease severity and greater rates of revision surgery. Similar relationships were noted for both cytokines when CRS with nasal polyps (CRSwNP) patients were analyzed separately. Th2-high CRS and Th2-low CRS were then categorized using a scaled IL-5/IL-13 metric. Th2-high CRS was characterized by an increased number of subjects with nasal polyps and comorbid asthma, and worse symptom and computed tomography (CT) scores.

conclusionThe Th2-associated cytokines, IL-5 and IL-13, are detectable in sinonasal mucus and their levels can be used to define Th2-high and Th2-low CRS. Identification of Th2-high and Th2-low endotypes using mucus-based biomarkers could facilitate stratification of CRS subgroups and guide personalized therapies.

Indexed as

BiomarkersChronic DiseaseFemaleHumansInterleukin-13Interleukin-5MaleMiddle AgedMucusNasal MucosaNasal PolypsProspective StudiesRhinitisSinusitisTh2 CellsBiomarkersIL13 protein, humanIL5 protein, humanInterleukin-13Interleukin-5biomarkerendotypeeosinophilsmucusrhinosinusitisTh2 cell

Identifiers

PMID29883053
PMCPMC6168400
OpenAlexW2806837647

What OpenQuestion holds

Textmetadata
LicenceTDM
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.