Evidence map›Paper›PMID 29202821›Full record

ArticleBMC pulmonary medicine2017

Effects of treatment changes on asthma phenotype prevalence and airway neutrophil function.

Collin R Brooks, Christine J Van Dalen, Elizabeth Harding, Ian F Hermans, Jeroen Douwes

Open access · goldAbstract read
In one paragraph

Article in BMC pulmonary medicine, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.4field-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

10 citing papers in PubMed, 22 citations in OpenAlex.

  1. Article
  2. Article
  3. Phenotype overlap in the natural history of asthma.European respiratory review : an official journal of the European Respiratory Society · 2023
    Review
  4. Article
  5. Which Therapy for Non-Type(T)2/T2-Low Asthma.Journal of personalized medicine · 2021
    Review
  6. Article
  7. Article
  8. Review
  9. Article
  10. Non-eosinophilic asthma: current perspectives.Journal of asthma and allergy · 2018
    Review
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

5 authors at 2 institutions in 1 country.

Collin R BrooksCentre for Public Health Research, Massey University Wellington Campus, Private Box 756, Wellington, 6140, New Zealand. C.R.Brooks@massey.ac.nz.
Christine J Van DalenCentre for Public Health Research, Massey University Wellington Campus, Private Box 756, Wellington, 6140, New Zealand.
Elizabeth HardingCentre for Public Health Research, Massey University Wellington Campus, Private Box 756, Wellington, 6140, New Zealand.
Ian F HermansMalaghan Institute of Medical Research, Wellington, New Zealand.
Jeroen DouwesCentre for Public Health Research, Massey University Wellington Campus, Private Box 756, Wellington, 6140, New Zealand.
Massey University · NZMalaghan Institute of Medical Research · NZ

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAsthma inflammatory phenotypes are often defined by relative cell counts of airway eosinophils/neutrophils. However, the importance of neutrophilia remains unclear, as does the effect of ICS treatment on asthma phenotypes and airway neutrophil function. The purpose of this study was to assess asthma phenotype prevalence/characteristics in a community setting, and, in a nested preliminary study, determine how treatment changes affect phenotype stability and inflammation, with particular focus on airway neutrophils.

methodsFifty adult asthmatics and 39 non-asthmatics were assessed using questionnaires, skin prick tests, spirometry, exhaled nitric oxide (FENO) measurement, and sputum induction. Twenty-one asthmatics underwent further assessment following treatment optimisation (n = 11) or sub-optimisation (n = 10).

resultsForty percent (20/50) had eosinophilic asthma (EA) and 8% had neutrophilic asthma. EA was associated with increased FENO, bronchodilator reversibility (BDR) and reduced lung function (p < 0.05). Following optimisation/sub-optimisation, the EA/NEA (non-eosinophilic asthma) phenotype changed in 11/21 (52%) asthmatics. In particular, fewer subjects had EA post treatment optimisation, but this was not statistically significant. However, a significant (p < 0.05) reduction in FENO, ACQ7 score, and BDR was observed after treatment optimisation, as well as an increase in FEV

conclusionsIn this community based population, non-eosinophilic asthma was common, less severe than EA, and at baseline most asthmatics showed no evidence of inflammation. In the nested change in treatment study, treatment optimisation was associated with reduced sputum eosinophils, improved symptoms and lung function, and enhanced neutrophil function, but a significant reduction in EA could not be demonstrated.

trial registrationThe nested change in treatment component of this study is registered at the Australia and New Zealand Clinical Trial Registry ( www.ANZCTR.org.au ) ACTRN12617001356358 . Registration date 27/09/2017. Retrospectively registered.

Indexed as

PhenotypeAdministration, InhalationAdolescentAdrenal Cortex HormonesAdultAgedAsthmaBreath TestsBronchodilator AgentsEosinophiliaFemaleForced Expiratory VolumeHumansInflammationMaleMiddle AgedAdrenal Cortex HormonesBronchodilator AgentsNitric OxideAsthmaEosinophilsInduced sputumInflammatory phenotypeNeutrophils

Identifiers

PMID29202821
PMCPMC5715501
OpenAlexW2774178399

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.