Evidence map›Paper›PMID 37857423›Full record

ArticleThe European respiratory journal2023

Clinical remission in severe asthma with biologic therapy: an analysis from the UK Severe Asthma Registry.

P Jane McDowell, Ron McDowell, John Busby, M Chad Eastwood, Pujan H Patel, David J Jackson, Adel Mansur, Mitesh Patel, Hassan Burhan, Simon Doe and 7 more

Registry-linked trialOpen access · hybridAbstract read
In one paragraph

Article in The European respiratory journal, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT07328035 (Remission in Adults With Severe Asthma in Thailand), which is not on this map. Cited by 71 papers.

0numbers the graph read from it
0cells of the map it votes in
71citing papers in PubMed
22.8field-weighted citation impact, top 1% 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.

NCT07328035 recruitingnot on this mapstarted 2026, after this paper: background citation

Remission in Adults With Severe Asthma in Thailand

TypeobservationalSponsorThammasat UniversityRan2026 to 2026Enrolled230ConditionsSevere Asthma, Asthma Control LevelArmsGlobal Initiative for Asthma (GINA) and Asthma Control Test (ACT) questionnaires, Spirometry, Fractional exhaled nitric oxide (FeNO) test, Blood eosinophil count (BEC)
3 · Its place in the literature

Who cites it

71 citing papers in PubMed, 130 citations in OpenAlex.

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11 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

17 authors at 12 institutions in 1 country.

P Jane McDowellWellcome Wolfson Centre for Experimental Medicine, School of Medicine, Dentistry and Biomedical Sciences, Queen's University, Belfast, UK.ORCID 0000-0003-2063-7992
Ron McDowellCentre for Public Health, School of Medicine, Dentistry and Biomedical Sciences, Queen's University, Belfast, UK janemcdowell@doctors.org.uk.
John BusbyCentre for Public Health, School of Medicine, Dentistry and Biomedical Sciences, Queen's University, Belfast, UK.
M Chad EastwoodWellcome Wolfson Centre for Experimental Medicine, School of Medicine, Dentistry and Biomedical Sciences, Queen's University, Belfast, UK.
Pujan H PatelRoyal Brompton and Harefield Hospitals, London, UK.
David J JacksonGuy's Severe Asthma Centre, Guy's Hospital, School of Immunology and Microbial Sciences, King's College London, London, UK.
Adel MansurUniversity of Birmingham and Heartlands Hospital, Birmingham, UK.
Mitesh PatelDepartment of Respiratory Medicine, University Hospitals Plymouth NHS Trust, Derriford Hospital, Plymouth, UK.
Hassan BurhanRoyal Liverpool University Hospital, Liverpool, UK.
Simon DoeThe Newcastle upon Tyne Hospitals NHS Foundation Trust, Newcastle upon Tyne, UK.
Rekha ChaudhuriNHS Greater Glasgow and Clyde Health Board, Gartnavel Hospital, Glasgow, UK.
Robin GoreAddenbrooke's Hospital, Cambridge University Hospitals NHS Foundation Trust, Cambridge, UK.
James W DoddAcademic Respiratory Unit, University of Bristol, Bristol, UK.ORCID 0000-0003-4805-5759
Deepak SubramanianUniversity Hospitals of Derby and Burton NHS Foundation Trust, Derby, UK.
Thomas BrownPortsmouth Hospitals NHS Trust, Portsmouth, UK.
Liam G HeaneyWellcome Wolfson Centre for Experimental Medicine, School of Medicine, Dentistry and Biomedical Sciences, Queen's University, Belfast, UK.
UK Severe Asthma Registry
Queen's University Belfast · GBCambridge University Hospitals NHS Foundation Trust · GBDerriford Hospital · GBGuy's Hospital · GBHarefield Hospital · GBHeartlands Hospital · GBNewcastle upon Tyne Hospitals NHS Foundation Trust · GBNHS Greater Glasgow and Clyde · GBPortsmouth Hospitals NHS Trust · GBUniversity Hospitals of Derby and Burton NHS Foundation Trust · GBUniversity of Bristol · GBUniversity of Liverpool · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundNovel biologic therapies have revolutionised the management of severe asthma with more ambitious treatment aims. Here we analyse the definition of clinical remission as a suggested treatment goal and consider the characteristics associated with clinical remission in a large, real-world severe asthma cohort.

methodsThis was a retrospective analysis of severe asthma patients registered in the UK Severe Asthma Registry (UKSAR) who met strict national access criteria for biologics. Patients had a pre-biologics baseline assessment and annual review. The primary definition of clinical remission applied included Asthma Control Questionnaire (ACQ)-5 <1.5 and no oral corticosteroids for disease control and forced expiratory volume in 1 s above lower limit of normal or no more than 100 mL less than baseline.

results18.3% of patients achieved the primary definition of remission. The adjusted odds of remission on biologic therapy were 7.44 (95% CI 1.73-31.95)-fold higher in patients with type 2 (T2)-high biomarkers. The adjusted odds of remission were lower in patients who were female (OR 0.61, 95% CI 0.45-0.93), obese (OR 0.49, 95% CI 0.24-0.65) or had ACQ-5 ≥1.5 (OR 0.19, 95% CI 0.12-0.31) pre-biologic therapy. The likelihood of remission reduced by 14% (95% CI 0.76-0.97) for every 10-year increase in disease duration. 12-21% of the cohort attained clinical remission depending on the definition applied; most of those who did not achieve remission failed to meet multiple criteria.

conclusions18.3% of patients achieved the primary definition of clinical remission. Remission was more likely in T2-high biomarker patients with shorter duration of disease and less comorbidity. Further research on the optimum time to commence biologics in severe asthma is required.

Indexed as

Anti-Asthmatic AgentsAsthmaBiological ProductsBiological TherapyBiomarkersFemaleHumansMaleRegistriesRetrospective StudiesUnited KingdomAnti-Asthmatic AgentsBiological ProductsBiomarkers

Identifiers

PMID37857423
PMCPMC10719453
OpenAlexW4387781980

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Registered trials

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.