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Introduction <p>Asthma is a heterogenous disease shaped by different inflammatory pathways. The aim is to investigate transcriptomic profiles in asthmatic patients and associate these with inflammation, airway damage and lung function.</p> Methods <p>Adult asthma patients attending the outpatient pneumology clinic in our tertiary center, underwent diagnostic sputum induction and upon consent remaining sputum RNA was used for bulk RNA-sequencing (<i>n</i> = 56) coupled with unsupervised clustering. A retrospective analysis of comorbidities was performed. Sputum cytokine mRNA levels were determined via qPCR. Airway damage markers were determined in sputum supernatant</p> Results <p>Unsupervised clustering subdivided all asthmatic patients in one of three clusters. Cluster 1 contained most of the pauci-granulocytic asthma patients in whom oxidative stress was upregulated and TLR-signalling and several cytokine pathways down-regulated. Cluster 2 had upregulated S100 family signalling pathway genes, was mostly associated to type 2 inflammation with elevated sputum eosinophils, epithelial damage, IL-4 mRNA levels and allergy. Asthma patients in cluster 3 had worse lung function, upregulated inflammatory genes, increased sputum neutrophils and calprotectin levels.</p> Conclusion <p>Three different asthma clusters could be identified bridging over the classical type 2/non-type 2 classification.</p> Clinical trial <p>ClinicalTrials.gov Identifier: NCT01224938 registered on 19 October 2010.</p>

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Sputum Transcriptomic Analysis and Clustering Reveals Insight Into Asthma Heterogeneity

  • 期刊论文

  • 发表日期：

    2025年8月20日

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  • Janne Goossens,
  • Anne-Charlotte Jonckheere,
  • Sien De Boodt,
  • Ellen Dilissen,
  • Nora Marain,
  • Tatjana Decaesteker,
  • Alvaro Cortes,
  • Jeroen A. Vanoirbeek,
  • Sven F. Seys,
  • Lieven Dupont,
  • Dominique M.A. Bullens

摘要

Introduction

Asthma is a heterogenous disease shaped by different inflammatory pathways. The aim is to investigate transcriptomic profiles in asthmatic patients and associate these with inflammation, airway damage and lung function.

Methods

Adult asthma patients attending the outpatient pneumology clinic in our tertiary center, underwent diagnostic sputum induction and upon consent remaining sputum RNA was used for bulk RNA-sequencing (n = 56) coupled with unsupervised clustering. A retrospective analysis of comorbidities was performed. Sputum cytokine mRNA levels were determined via qPCR. Airway damage markers were determined in sputum supernatant

Results

Unsupervised clustering subdivided all asthmatic patients in one of three clusters. Cluster 1 contained most of the pauci-granulocytic asthma patients in whom oxidative stress was upregulated and TLR-signalling and several cytokine pathways down-regulated. Cluster 2 had upregulated S100 family signalling pathway genes, was mostly associated to type 2 inflammation with elevated sputum eosinophils, epithelial damage, IL-4 mRNA levels and allergy. Asthma patients in cluster 3 had worse lung function, upregulated inflammatory genes, increased sputum neutrophils and calprotectin levels.

Conclusion

Three different asthma clusters could be identified bridging over the classical type 2/non-type 2 classification.

Clinical trial

ClinicalTrials.gov Identifier: NCT01224938 registered on 19 October 2010.