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Clustering lung function and symptom profiles for asthma risk stratification

Clustering lung function and symptom profiles for asthma risk stratification
Clustering lung function and symptom profiles for asthma risk stratification
Asthma is a heterogeneous condition often studied through wheeze alone, yet the interplay between lung function and reported symptoms remains underexplored. To capture this heterogeneity, we applied Bayesian Profile Regression to data from school-age children in two prospective birth cohorts, integrating airway hyperresponsiveness, lung function, bronchodilator reversibility, allergic sensitisation, reported symptoms, and physician diagnosis. In the Manchester Allergy and Asthma Study (discovery cohort), five reproducible clusters were identified: HA-LLF (high asthma-low lung function), HA-NLF (high asthma normal lung function), LA-RLF (low asthma-reduced lung function), LA-NLF (low asthma normal lung function), and MA-NLF (moderate asthma normal lung function). The HA-LLF and HA-NLF clusters had very high asthma prevalence (80–100%), but differed markedly in lung function, airway responsiveness, bronchodilator reversibility, sensitisation, and symptom burden. The LA-RLF and LA-NLF clusters with low asthma prevalence (< 5%) displayed contrasting lung function profiles, while MA-NLF (~ 50% asthma prevalence) was largely defined by prominent symptoms such as chest tightness and shortness of breath. These subtypes were replicated in an independent cohort, Isle of Wight. Our findings demonstrate that integrating physiological, immunological, and symptom-based measures yields clinically meaningful asthma subtypes beyond wheeze-based definitions and may support more precise disease classification.
Asthma, Bayesian Profile regression, Birth cohorts, Childhood, Disease subtyping
2045-2322
Cucco, Alex
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Simpson, Angela
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Murray, Clare
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Roberts, Graham C.
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Holloway, John W.
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Arshad, S. Hasan
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Custovic, Adnan
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Fontanella, Sara
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Cucco, Alex
572ce496-405d-49e6-bc2f-585a4f3c55e3
Simpson, Angela
5591f945-0ead-46a3-a866-b7bea84a2a83
Murray, Clare
aca69df6-149c-401c-842f-5b2d8042edf1
Roberts, Graham C.
ea00db4e-84e7-4b39-8273-9b71dbd7e2f3
Holloway, John W.
4bbd77e6-c095-445d-a36b-a50a72f6fe1a
Arshad, S. Hasan
917e246d-2e60-472f-8d30-94b01ef28958
Custovic, Adnan
17d8d092-73b8-44fb-bf48-5cea7b29e3fc
Fontanella, Sara
6c29b69f-edd6-4414-a8fd-c47241976aa5

Cucco, Alex, Simpson, Angela, Murray, Clare, Roberts, Graham C., Holloway, John W., Arshad, S. Hasan, Custovic, Adnan and Fontanella, Sara (2026) Clustering lung function and symptom profiles for asthma risk stratification. Scientific Reports, 16 (1), [3110]. (doi:10.1038/s41598-025-32977-w).

Record type: Article

Abstract

Asthma is a heterogeneous condition often studied through wheeze alone, yet the interplay between lung function and reported symptoms remains underexplored. To capture this heterogeneity, we applied Bayesian Profile Regression to data from school-age children in two prospective birth cohorts, integrating airway hyperresponsiveness, lung function, bronchodilator reversibility, allergic sensitisation, reported symptoms, and physician diagnosis. In the Manchester Allergy and Asthma Study (discovery cohort), five reproducible clusters were identified: HA-LLF (high asthma-low lung function), HA-NLF (high asthma normal lung function), LA-RLF (low asthma-reduced lung function), LA-NLF (low asthma normal lung function), and MA-NLF (moderate asthma normal lung function). The HA-LLF and HA-NLF clusters had very high asthma prevalence (80–100%), but differed markedly in lung function, airway responsiveness, bronchodilator reversibility, sensitisation, and symptom burden. The LA-RLF and LA-NLF clusters with low asthma prevalence (< 5%) displayed contrasting lung function profiles, while MA-NLF (~ 50% asthma prevalence) was largely defined by prominent symptoms such as chest tightness and shortness of breath. These subtypes were replicated in an independent cohort, Isle of Wight. Our findings demonstrate that integrating physiological, immunological, and symptom-based measures yields clinically meaningful asthma subtypes beyond wheeze-based definitions and may support more precise disease classification.

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s41598-025-32977-w - Version of Record
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Accepted/In Press date: 15 December 2025
e-pub ahead of print date: 24 December 2025
Published date: 23 January 2026
Keywords: Asthma, Bayesian Profile regression, Birth cohorts, Childhood, Disease subtyping

Identifiers

Local EPrints ID: 509323
URI: http://eprints.soton.ac.uk/id/eprint/509323
ISSN: 2045-2322
PURE UUID: 6d8b65d8-95eb-4431-a726-71e4454c2f31
ORCID for Graham C. Roberts: ORCID iD orcid.org/0000-0003-2252-1248
ORCID for John W. Holloway: ORCID iD orcid.org/0000-0001-9998-0464

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Date deposited: 18 Feb 2026 17:43
Last modified: 19 Feb 2026 02:39

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Contributors

Author: Alex Cucco
Author: Angela Simpson
Author: Clare Murray
Author: S. Hasan Arshad
Author: Adnan Custovic
Author: Sara Fontanella

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