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Related Concept Videos

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Related Experiment Video

Updated: May 14, 2025

Author Spotlight: Development and Characterization of an In Vitro Model to Study Chronic Cigarette Smoke Exposure and Its Impact on Airway Epithelial Cells in COPD Research
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Author Spotlight: Development and Characterization of an In Vitro Model to Study Chronic Cigarette Smoke Exposure and Its Impact on Airway Epithelial Cells in COPD Research

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Lung Function Decline and Airflow Limitation Risk in Preserved Ratio Impaired Spirometry Subtypes by Smoking Status.

Cuiqiong Dai1, Fan Wu2, Jia Tian3

  • 1State Key Laboratory of Respiratory Disease & National Clinical Research Center for Respiratory Disease & Guangzhou Institute of Respiratory Health & National Center for Respiratory Medicine & Department of Pulmonary and Critical Care Medicine, The First Affiliated Hospital of Guangzhou Medical University, Guangzhou Medical University, Guangzhou, Guangdong, China.

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PubMed
Summary

Pre-respiratory illness syndrome (PRISm) may precede COPD in both smokers and never-smokers. Both never-smokers with PRISm (NS-PRISm) and ever-smokers with PRISm (ES-PRISm) show increased airflow limitation risk.

Keywords:
PRISmairflow limitationlung function declinesmoking status

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Area of Science:

  • Pulmonary Medicine
  • Respiratory Health
  • Epidemiology

Background:

  • Pre-respiratory illness syndrome (PRISm) is recognized as a precursor to Chronic Obstructive Pulmonary Disease (COPD).
  • However, the influence of smoking status on the progression from PRISm to COPD remains incompletely understood.

Purpose of the Study:

  • To investigate whether annual lung function decline and the risk of developing airflow limitation differ among subtypes of PRISm based on smoking status.
  • To compare these outcomes between never-smokers with PRISm (NS-PRISm), ever-smokers with PRISm (ES-PRISm), and a healthy control group.

Main Methods:

  • Analysis of a 15-year population-based prospective cohort study involving 2850 participants.
  • Categorization of participants into three groups: normal controls (never-smokers with normal spirometry), NS-PRISm, and ES-PRISm.
  • Comparison of annual lung function decline rates and the incidence of airflow limitation across the defined groups.

Main Results:

  • The ES-PRISm group exhibited a significantly faster annual lung function decline and a higher risk of developing airflow limitation compared to the NS-PRISm group.
  • Both NS-PRISm and ES-PRISm groups demonstrated an increased risk of airflow limitation compared to the normal control group.
  • Further analysis of ES-PRISm revealed that current and former smokers with PRISm showed accelerated lung function decline and elevated airflow limitation risk relative to NS-PRISm.

Conclusions:

  • Findings suggest that both NS-PRISm and ES-PRISm are potential precursors to COPD.
  • PRISm should be considered in both smoking and non-smoking populations for COPD risk assessment.
  • Early identification and intervention for PRISm are crucial for preventing COPD development.