4.7 Article

The Combined Value of Type2 Inflammatory Markers in Chronic Obstructive Pulmonary Disease

Journal

JOURNAL OF CLINICAL MEDICINE
Volume 11, Issue 10, Pages -

Publisher

MDPI
DOI: 10.3390/jcm11102791

Keywords

COPD; exacerbation; fraction of exhaled nitric oxide; eosinophil; type2 immune response

Funding

  1. National Natural Science Foundation of China [81871100, 81600056]
  2. National Key R&D Program of China [2020YFC2009000, 2020YFC2009001]
  3. Scientific Research Project of Shanghai Science and Technology Commission [21140902500]
  4. Scientific the Research Project of Shanghai Municipal Health Commission [202140036]
  5. Shanghai Municipal Key Clinical Specialty [shslczdzk02801]
  6. Bethune Research and Development Fund Project [BJ-RW2020002J]
  7. Investigator-Initiated Clinical Trials Foundation of the Huadong Hospital [HDLC2022018]
  8. Shanghai Health System Young Talent Fund Project Hengjie-Special Support Program [2022-020]

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The combined use of fraction of exhaled nitric oxide (FeNO) level and blood eosinophil count strengthens their association with acute exacerbation in chronic obstructive pulmonary disease (COPD). Simultaneously increased FeNO level and blood eosinophil count can predict mild and moderate acute exacerbation in COPD.
The roles of type2 inflammatory markers in chronic airway diseases have been assessed in previous studies. However, the relationship between the combined value of these biomarkers and chronic obstructive pulmonary disease (COPD) has not been fully elucidated. We aimed to investigate the roles of the combined value of the fraction of exhaled nitric oxide (FeNO) level and blood eosinophil count in COPD and the predictive capability of these biomarkers. In total, 266 patients were included in our analysis. When the two type2 biomarkers were assessed separately, there were limited correlations between either increased FeNO level or blood eosinophil count and decreased incidence of total exacerbation or frequency of mild exacerbation. Combining these two biomarkers strengthened their association with both incidence and frequency of acute exacerbation. In addition, during further assessment, simultaneously increased FeNO level and blood eosinophil count were associated with both mild and moderate acute exacerbation. Among the subjects included in this analysis, although the predictive capability was improved when these two biomarkers were combined, the improvement was not statistically significant, indicating the need to increase the sample size. The combination of FeNO level and blood eosinophil count exhibited strong and independent additive value in the assessment of acute exacerbation in COPD; simultaneously increased FeNO level and blood eosinophil count played a protective role in progression of COPD.

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