TY - JOUR
T1 - Determinants of airway morphology in asthma
T2 - Inflammatory and noninflammatory factors
AU - Shimizu, Kaoruko
AU - Tanabe, Naoya
AU - Kimura, Hirokazu
AU - Miyata, Jun
AU - Chubachi, Shotaro
AU - Nakamaru, Yuji
AU - Oguma, Akira
AU - Wakazono, Nobuyasu
AU - Okada, Kazufumi
AU - Goudarzi, Houman
AU - Tsujino, Ichizo
AU - Makira, Hironi
AU - Nishimura, Masaharu
AU - Konno, Satoshi
N1 - Publisher Copyright:
© 2025 The Author(s)
PY - 2025/11
Y1 - 2025/11
N2 - Background: Patients with asthma may exhibit impaired airway tree morphology. The impact of difficult-to-treat traits on airway tree morphology remains unclear. Objective: We sought to identify determinants of total airway branch count (TAC) detectable via computed tomography and explore associated blood and sputum biomarkers in nonsmokers and smokers with asthma. Methods: Baseline computed tomography scans and pulmonary function tests (spirometry, diffusion capacity of carbon monoxide, and lung volume) were analyzed from the Hokkaido Severe Asthma Cohort (N = 190). TAC, segmental airway, visually evident mucus plugging and bronchiectasis, and parenchymal and extrapulmonary indices, such as the Lund-Mackay score, were evaluated. Relationships between TAC, difficult-to-treat traits, and blood/sputum biomarkers were analyzed using crude or multivariable regression models, adjusted for demographic factors. Results: Blood or sputum eosinophilia, mucus plugs, high body mass index (BMI), asthma duration, and higher Lund-Mackay score correlated with low TAC. Low TAC was linked to airflow obstruction and heterogeneous ventilation (low alveolar volume/total lung capacity). BMI was inversely associated with TAC, independent of age, sex, smoking status, sputum eosinophil ratio, and asthma duration. The presence of bronchiectasis correlated with an increase in TAC. Sputum IL-5, IL-6, RANTES, and circulating YKL-40 (chitinase-3-like-1 protein) and leptin also inversely correlated with TAC. Conclusions: BMI, asthma duration, sinusitis, and the presence of bronchiectasis are significant determinants of airway tree morphology in asthma, alongside inflammation and mucus plugs. Both inflammatory and noninflammatory biomarkers were associated with low TAC.
AB - Background: Patients with asthma may exhibit impaired airway tree morphology. The impact of difficult-to-treat traits on airway tree morphology remains unclear. Objective: We sought to identify determinants of total airway branch count (TAC) detectable via computed tomography and explore associated blood and sputum biomarkers in nonsmokers and smokers with asthma. Methods: Baseline computed tomography scans and pulmonary function tests (spirometry, diffusion capacity of carbon monoxide, and lung volume) were analyzed from the Hokkaido Severe Asthma Cohort (N = 190). TAC, segmental airway, visually evident mucus plugging and bronchiectasis, and parenchymal and extrapulmonary indices, such as the Lund-Mackay score, were evaluated. Relationships between TAC, difficult-to-treat traits, and blood/sputum biomarkers were analyzed using crude or multivariable regression models, adjusted for demographic factors. Results: Blood or sputum eosinophilia, mucus plugs, high body mass index (BMI), asthma duration, and higher Lund-Mackay score correlated with low TAC. Low TAC was linked to airflow obstruction and heterogeneous ventilation (low alveolar volume/total lung capacity). BMI was inversely associated with TAC, independent of age, sex, smoking status, sputum eosinophil ratio, and asthma duration. The presence of bronchiectasis correlated with an increase in TAC. Sputum IL-5, IL-6, RANTES, and circulating YKL-40 (chitinase-3-like-1 protein) and leptin also inversely correlated with TAC. Conclusions: BMI, asthma duration, sinusitis, and the presence of bronchiectasis are significant determinants of airway tree morphology in asthma, alongside inflammation and mucus plugs. Both inflammatory and noninflammatory biomarkers were associated with low TAC.
KW - Airway remodeling
KW - Lund-Mackay score
KW - asthma
KW - body mass index
KW - computed tomography
KW - eosinophils
KW - leptin
KW - mucus plugs
KW - obesity
KW - type 2 inflammation
UR - https://www.scopus.com/pages/publications/105014859728
UR - https://www.scopus.com/pages/publications/105014859728#tab=citedBy
U2 - 10.1016/j.jacig.2025.100555
DO - 10.1016/j.jacig.2025.100555
M3 - Article
AN - SCOPUS:105014859728
SN - 2772-8293
VL - 4
JO - Journal of Allergy and Clinical Immunology: Global
JF - Journal of Allergy and Clinical Immunology: Global
IS - 4
M1 - 100555
ER -