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Chinese Journal of Lung Diseases(Electronic Edition) ›› 2025, Vol. 18 ›› Issue (06): 955-960. doi: 10.3877/cma.j.issn.1674-6902.2025.06.017

• Original Article • Previous Articles    

Sttudy on relationship between blood eosinophil count and alveolar damage in patients and chronic obstructive pulmonary disease with emphysema

Miaomiao Yang1, Xiang Gu2, Liu Yang1, Tianyu Sun1, Menglin Wang1, Tuo Zhang1,(), Ting Wang2   

  1. 1Department of Laboratory, Jiangsu Provincial People′s Hospital Suqian Hospital, Suqian 223800, China
    2Department of Respiratory Medicine, Jiangsu Provincial People′s Hospital Suqian Hospital, Suqian 223800, China
  • Received:2025-09-09 Online:2025-12-25 Published:2026-01-12
  • Contact: Tuo Zhang

Abstract:

Objective

To investigate the relationship between eosinophil (EOS) count and alveolar damage in patients with chronic obstructive pulmonary disease (COPD) complicated with emphysema.

Methods

A total of 186 patients with COPD and emphysema admitted to our hospital from January 2021 to June 2025 were selected. EOS counts were measured, and patients underwent chest computerized tomography (CT) scans, pulmonary function tests, and cardiopulmonary exercise testing (CPET). Spearman analysis was used to analyze the correlations between EOS count and CT parameters, pulmonary function, and CPET parameters. Multiple linear regression was employed to adjust for confounding factors.

Results

Among the 186 patients, 82 were identified as the EOS phenotype (EOS ≥300/μl) and 104 as the non-EOS phenotype (EOS<300/μl). The use of bronchodilators was higher in the EOS phenotype group 63 cases( 76.83%) compared to the non-EOS phenotype group 56 cases(53.85%) (P=0.001), and the neutrophil count was lower in the EOS phenotype group (P=0.027). Spearman correlation analysis showed that in the EOS phenotype group, EOS count was positively correlated with the expiratory to inspiratory ratio of mean lung density (E/I) (rs=0.484, P=0.000), the wall area percentage of the 5th generation apical segment bronchus (B1 5th WA%) (rs=0.396, P=0.000), and the wall thickness of the 5th generation apical segment airway (B1 5th WT) (rs=0.245, P=0.041). It was negatively correlated with the peak of minute ventilation (VEpeak) (rs=-0.239, P=0.030), maximum voluntary ventilation (MVV) (rs=-0.442, P=0.000), peak heart rate (HRpeak) (rs=-0.336, P=0.002), oxygen saturation (SpO2) (rs=-0.230, P=0.037), Z score of forced expiratory volume in one second (FEV1 Z-score) (rs=-0.484, P=0.000), Z score of FEV1 to forced vital capacity ratio (FEV1/FVCZ-score) (rs=-0.488, P=0.000), Z score of diffusion capacity for carbon monoxide of the lung (DLCO Z-score) (rs=-0.230, P=0.038), and Z score of alveolar ventilation (VAZ-score) (rs=-0.231, P=0.037). In the non-EOS phenotype group, EOS count was negatively correlated with diffusion capacity for carbon monoxide per liter of alveolar volume (KCO) (rs=-0.200, P=0.042). Multiple linear regression showed that in the EOS phenotype group, EOS count was associated with E/I (P=0.000), B1 5th WA% (P=0.000), B1 5th WT (P=0.041), VEpeak (P=0.008), MVV (P=0.000), VR (P=0.004), FEV1 Z-score (P=0.000), FEV1/FVCZ-score (P=0.000), and VAZ-score(P=0.029). No such associations were found in non-EOS patients.

Conclusion

Alveolar damage in patients with COPD and emphysema is associated with airway eosinophilic inflammation. The EOS phenotype is associated with more severe emphysema and alveolar damage.

Key words: Chronic obstructive pulmonary disease, Emphysema, Eosinophils, Alveolar damage, Lung function

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