Predictive Value of Combining Inflammatory Biomarkers and Rapid Decline of FEV1 for COPD in Chinese Population: A Prospective Cohort Study

Int J Chron Obstruct Pulmon Dis. 2019 Dec 5:14:2825-2833. doi: 10.2147/COPD.S223869. eCollection 2019.

Abstract

Background: In China, the high prevalence and mortality rate of Chronic Obstructive Pulmonary Disease (COPD) and the poor intervention effect makes it into a heavy social burden. The main reason is that the current diagnosis of COPD mainly based on the static lung function, which is difficult for early intervention. Through matching a predictive model for high-risk groups of COPD that rewards FEV1 rapid decline as the core, we will establish the early warning model and prove its validity and socio-economic value.

Methods: This is a multi-center, prospective, cohort study. A total of 10,000 people aged 40∼75 without lung disease will be recruited and followed for 3 years. Some questionnaires such as St George's Respiratory Questionnaire (SGRQ), income class, educational level, comorbidity, smoking habit, and biomass smoke exposure history will be collected. The baseline level of Interleukin 6 (IL-6), high-sensitivity C-reactive Protein (hs-CRP), microRNAs-23a (miR-23a) in peripheral blood and pH value in exhaled breath condensate (EBC) will be measured, lung spirometry will be tested in the first, second, and fourth years. Primary outcome is the incidence of COPD, multivariate regression analysis will be used to establish the predictive model for COPD in China.

Discussion: With the rapid decline of lung function as the core and the baseline inflammatory biomarkers in peripheral blood and pH of the exhaled breath condensate as affecting factors, a predictive model to achieve early detection of high-risk COPD groups will be established and promoted.

Trial registration: This study has been registered at www.ClinicalTrials.gov (registration identifier: NCT03532893) on 21 May 2018, https://register.clinicaltrials.gov.

Keywords: COPD; EBC; decline in FEV1; inflammatory biomarkers; microRNA-23a.

Publication types

  • Multicenter Study
  • Validation Study

MeSH terms

  • Adult
  • Aged
  • Biomarkers / blood
  • C-Reactive Protein / metabolism
  • China
  • Disease Progression
  • Female
  • Forced Expiratory Volume*
  • Humans
  • Inflammation Mediators / blood*
  • Interleukin-6 / blood
  • Lung / physiopathology*
  • Male
  • MicroRNAs / blood
  • Middle Aged
  • Predictive Value of Tests
  • Prognosis
  • Prospective Studies
  • Pulmonary Disease, Chronic Obstructive / blood
  • Pulmonary Disease, Chronic Obstructive / diagnosis*
  • Pulmonary Disease, Chronic Obstructive / physiopathology
  • Reproducibility of Results
  • Research Design
  • Time Factors

Substances

  • Biomarkers
  • IL6 protein, human
  • Inflammation Mediators
  • Interleukin-6
  • MIRN23a microRNA, human
  • MicroRNAs
  • C-Reactive Protein

Associated data

  • ClinicalTrials.gov/NCT03532893

Grants and funding

The study is supported by grant 2017YFC1309500 from the National Key Research and Development Plan sponsored by the Ministry of Science and Technology of the People’s Republic of China. It is a governmental funding and the study protocol has undergone peer-review by the funding body.