Longitudinal analysis to better characterize Asthma-COPD overlap syndrome: Findings from an adult asthma cohort in Korea (COREA)

Clin Exp Allergy. 2019 May;49(5):603-614. doi: 10.1111/cea.13339. Epub 2019 Feb 14.

Abstract

Background: Asthma-chronic obstructive pulmonary disease (COPD) overlap syndrome (ACOS), which has received much attention, has not been unanimously defined.

Objective: In this study, we tried to demonstrate that longitudinally defined ACOS is more useful in the real world than blending patients with asthma and COPD.

Methods: The study patients had undergone two consecutive pulmonary function tests measured at least 3 months apart (n = 1889). We selected the patients who had positive bronchodilator response or methacholine provocation tests (n = 959). Next, we defined ACOS as a patient with a persistent airflow obstruction [forced expiratory volume in 1 second (FEV1)/forced vital capacity <0.7] that was identified twice consecutively by an interval of at least 3 months (n = 228).

Results: The proportions of patients who were older, male and smokers were significantly higher, and baseline lung function was lower in patients with ACOS. In the longitudinal analysis, the mean change in lung function was high, and a greater decline in FEV1 was observed in patients with ACOS. In addition, we compared ACOS and severe asthma, and we also performed a cluster analysis and compared the results with our definition of ACOS. According to our definition, ACOS is an independent subtype with distinctive characteristics. Finally, a genome-wide association study (GWAS) was performed to identify genetic variations associated with ACOS, but no significant single nucleotide polymorphisms were identified.

Conclusion: Our findings suggest that ACOS should be defined longitudinally and considered as an independent subgroup distinguished by inherited environmental factors rather than as a genetically distinct independent group.

Keywords: asthma; asthma-chronic obstructive pulmonary disease overlap syndrome; cluster analysis; genome-wide association study; longitudinal studies.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Age Factors
  • Aged
  • Asthma-Chronic Obstructive Pulmonary Disease Overlap Syndrome / diagnosis
  • Asthma-Chronic Obstructive Pulmonary Disease Overlap Syndrome / epidemiology*
  • Asthma-Chronic Obstructive Pulmonary Disease Overlap Syndrome / etiology
  • Asthma-Chronic Obstructive Pulmonary Disease Overlap Syndrome / therapy
  • Biomarkers
  • Cluster Analysis
  • Disease Management
  • Disease Susceptibility
  • Female
  • Genome-Wide Association Study
  • Humans
  • Longitudinal Studies
  • Male
  • Middle Aged
  • Phenotype
  • Public Health Surveillance
  • Republic of Korea / epidemiology
  • Respiratory Function Tests
  • Severity of Illness Index

Substances

  • Biomarkers