Evidence map›Paper›PMID 34728474›Full record

ArticleBMJ open respiratory research2021

Enhanced airway sensory nerve reactivity in non-eosinophilic asthma.

Hajar Ali, Collin Brooks, Julian Crane, Richard Beasley, Stephen Holgate, Peter Gibson, Philip Pattemore, Yu-Chieh Tzeng, Thorsten Stanley, Neil Pearce and 1 more

Open access · goldAbstract read
In one paragraph

Article in BMJ open respiratory research, 2021. 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
0.6field-weighted citation impact, top 33% 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, 9 citations in OpenAlex.

  1. Neuroplasticity and neuroimmune interactions with type 2 inflammation in asthma.European respiratory review : an official journal of the European Respiratory Society · 2026
    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

11 authors at 6 institutions in 3 countries.

Hajar AliCentre for Public Health Research, Massey University, Wellington, New Zealand.
Collin BrooksCentre for Public Health Research, Massey University, Wellington, New Zealand c.r.brooks@massey.ac.nz.
Julian CraneSchool of Medicine and Health Sciences, University of Otago, Wellington, New Zealand.
Richard BeasleyMedical Research Institute of New Zealand, Wellington, New Zealand.
Stephen HolgateUniversity of Southampton, Southampton, UK.
Peter GibsonDepartment of Respiratory and Sleep Medicine, John Hunter Hospital, Newcastle, New South Wales, Australia.
Philip PattemoreDepartment of Paediatrics, University of Otago, Christchurch, New Zealand.
Yu-Chieh TzengCentre for Translational Physiology, University of Otago, Wellington, New Zealand.
Thorsten StanleyDepartment of Paediatrics and Child Health, University of Otago, Wellington, New Zealand.
Neil PearceDepartment of Non-communicable Disease Epidemiology and Medical Statistics, London School of Hygiene and Tropical Medicine, London, UK.
Jeroen DouwesCentre for Public Health Research, Massey University, Wellington, New Zealand.
University of Otago · NZMassey University · NZJohn Hunter Hospital · AULondon School of Hygiene & Tropical Medicine · GBMedical Research Institute of New Zealand · NZUniversity of Southampton · GB

Funding

Medical Research Council G0800766
6 · The paper itself

Abstract

backgroundNeural mechanisms may play an important role in non-eosinophilic asthma (NEA). This study compared airway sensory nerve reactivity, using capsaicin challenge, in eosinophilic asthma (EA) and NEA and non-asthmatics.

methodsThirty-eight asthmatics and 19 non-asthmatics (aged 14-21 years) underwent combined hypertonic saline challenge/sputum induction, fractional exhaled nitric oxide, atopy and spirometry tests, followed by capsaicin challenge. EA and NEA were defined using a sputum eosinophil cut-point of 2.5%. Airway hyperreactivity was defined as a ≥15% drop in FEV

resultsNon-eosinophilic asthmatics (n=20) had heightened capsaicin sensitivity (lower C5) compared with non-asthmatics (n=19) (geometric mean C5: 58.3 µM, 95% CI 24.1 to 141.5 vs 193.6 µM, 82.2 to 456.0; p<0.05). NEA tended to also have greater capsaicin sensitivity than EA, with the difference in capsaicin sensitivity between NEA and EA being of similar magnitude (58.3 µM, 24.1 to 141.5 vs 191.0 µM, 70.9 to 514.0) to that observed between NEA and non-asthmatics; however, this did not reach statistical significance (p=0.07). FEV

conclusionNEA, but not EA, showed enhanced capsaicin sensitivity compared with non-asthmatics. Sensory nerve reactivity may therefore play an important role in the pathophysiology of NEA.

Indexed as

AsthmaPulmonary EosinophiliaEosinophilsFractional Exhaled Nitric Oxide TestingHumansSputumasthmaasthma epidemiologyasthma mechanismspaediatric asthma

Identifiers

PMID34728474
PMCPMC8565536
OpenAlexW3208739820

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.