Introduction: Acute exacerbations of COPD are responsible for 60% of health costs, re-duce patients' quality of life, and accelerate disease progression. COPD endotypes are expected to provide new insights about clinical phenotypic variability and therapeutic response between indivi-duals through certain biomarker approaches. Objective: Our study aims to identify the relationship between COPD endotypes and exacerbation events. Methods: In this cross-sectional study design, participants with stable COPD (n=40) were recruit-ed from the outpatient clinic at Airlangga University Hospital in March-August 2022. Blood was obtained for endotype's biomarker examination, such as α1-antitrypsin (AAT), IL-17A, neutrophil, and eosinophil count. The relationship between COPD endotypes and exacerbation events was an-alyzed using a non-parametric statistical test. Result: The lower limit normal of AAT levels obtained was 12.85ng/ml; 47.5% of subjects have low AAT levels. The average IL-17A levels and blood neutrophil counts were 0.478 ± 0.426 pg/ml and 5,916.95 ± 3,581.08 cells/μl, respectively. The average blood eosinophil count was 298.35 ± 280.44 cells/μl, 16 of 40 (40%) subjects with blood eosinophil count > 300 cells/μl. No significant association was observed between AAT levels (p = 1.000), IL-17A levels (p = 0.944), and blood eosinophil count (p = 0.739) with exacerbation events-only blood neutrophil count (p = 0.033) found to have a significant association with exacerbation events in COPD. Conclusion: AAT levels, IL-17A levels, and blood eosinophil count were not significantly related to exacerbation events in COPD patients. In comparison, blood neutrophil count was the only one associated considerably with exacerbation events. Further research about COPD endotypes is needed to identify exacerbation susceptibility as a precision treatment strategy.

Original languageEnglish
Pages (from-to)31-37
Number of pages7
JournalCurrent Respiratory Medicine Reviews
Issue number1
Publication statusPublished - 2024


  • AAT
  • acute exacerbation
  • blood eosinophil
  • COPD endotype
  • eosinophilic inflammation
  • neutrophilic inflammation


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