Evidence map›Paper›PMID 28833810›Full record

Trial reportClinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology2018

Features of asthma which provide meaningful insights for understanding the disease heterogeneity.

M Deliu, T S Yavuz, M Sperrin, D Belgrave, U M Sahiner, C Sackesen, O Kalayci, A Custovic

Abstract readClinical TrialMulticenter Study
In one paragraph

Trial report in Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing 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

31 citing papers in PubMed.

  1. Longitudinal trajectories of severe wheeze exacerbations from infancy to school age and their association with early-life risk factors and late asthma outcomes.Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology · 2020
    Trial
  2. Features of asthma which provide meaningful insights for understanding the disease heterogeneity.Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology · 2018
    Trial
  3. Review
  4. Unsupervised Machine Learning Identifies Asthma Phenotypes in the Population-Based West Sweden Asthma Study.Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology · 2026
    Article
  5. Review
  6. Article
  7. Review
  8. Article
  9. Article
  10. Review
  11. Social inequalities in childhood asthma.The World Allergy Organization journal · 2024
    Review
  12. Review
  13. Article
  14. Machine learning: A modern approach to pediatric asthma.Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology · 2022
    Review
  15. Review
  16. Recurrent Severe Preschool Wheeze: From Prespecified Diagnostic Labels to Underlying Endotypes.American journal of respiratory and critical care medicine · 2021
    Article
  17. Review
  18. Review
  19. 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

8 authors.

M DeliuDivision of Informatics, Imaging and Data Sciences, Faculty of Biology, Medicine and Health, University of Manchester, Manchester, UK.ORCID 0000-0002-6254-2708
T S YavuzDepartment of Pediatric Allergy, Gulhane School of Medicine, Ankara, Turkey.
M SperrinDivision of Informatics, Imaging and Data Sciences, Faculty of Biology, Medicine and Health, University of Manchester, Manchester, UK.
D BelgraveDepartment of Medicine, Section of Paediatrics, Imperial College London, London, UK.
U M SahinerPediatric Allergy and Asthma Unit, Hacettepe University School of Medicine, Ankara, Turkey.
C SackesenSchool of Medicine, Pediatric Allergy Unit, Koc University, Istanbul, Turkey.
O KalayciPediatric Allergy and Asthma Unit, Hacettepe University School of Medicine, Ankara, Turkey.
A CustovicDepartment of Medicine, Section of Paediatrics, Imperial College London, London, UK.

Funding

Medical Research Council G1000758Medical Research Council MC_PC_13042Medical Research Council MR/K002449/1Medical Research Council MR/K002449/2Medical Research Council MR/K006665/1Medical Research Council MR/M015181/1
6 · The paper itself

Abstract

backgroundData-driven methods such as hierarchical clustering (HC) and principal component analysis (PCA) have been used to identify asthma subtypes, with inconsistent results.

objectiveTo develop a framework for the discovery of stable and clinically meaningful asthma subtypes.

methodsWe performed HC in a rich data set from 613 asthmatic children, using 45 clinical variables (Model 1), and after PCA dimensionality reduction (Model 2). Clinical experts then identified a set of asthma features/domains which informed clusters in the two analyses. In Model 3, we reclustered the data using these features to ascertain whether this improved the discovery process.

resultsCluster stability was poor in Models 1 and 2. Clinical experts highlighted four asthma features/domains which differentiated the clusters in two models: age of onset, allergic sensitization, severity, and recent exacerbations. In Model 3 (HC using these four features), cluster stability improved substantially. The cluster assignment changed, providing more clinically interpretable results. In a 5-cluster model, we labelled the clusters as: "Difficult asthma" (n = 132); "Early-onset mild atopic" (n = 210); "Early-onset mild non-atopic: (n = 153); "Late-onset" (n = 105); and "Exacerbation-prone asthma" (n = 13). Multinomial regression demonstrated that lung function was significantly diminished among children with "Difficult asthma"; blood eosinophilia was a significant feature of "Difficult," "Early-onset mild atopic," and "Late-onset asthma." Children with moderate-to-severe asthma were present in each cluster. CONCLUSIONS AND CLINICAL RELEVANCE: An integrative approach of blending the data with clinical expert domain knowledge identified four features, which may be informative for ascertaining asthma endotypes. These findings suggest that variables which are key determinants of asthma presence, severity, or control may not be the most informative for determining asthma subtypes. Our results indicate that exacerbation-prone asthma may be a separate asthma endotype and that severe asthma is not a single entity, but an extreme end of the spectrum of several different asthma endotypes.

Indexed as

Models, ImmunologicalSeverity of Illness IndexAdolescentAsthmaChildFemaleHumansMaleallergic sensitizationasthmachildhoodcluster analysisendotypesphenotypessevere asthma

Identifiers

PMID28833810
PMCPMC5763358

What OpenQuestion holds

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Registered trials

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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.