Pulmonary Disease, Chronic Obstructive
Conditions
Brief summary
This is a 3-year longitudinal study designed to establish a personalized prediction and prevention system for acute exacerbations of chronic obstructive pulmonary disease (AECOPD). Data will be prospectively collected from patients with chronic obstructive pulmonary disease (COPD) and healthy control participants, including clinical characteristics, pathophysiological parameters, etiological factors, and immunological information. These data will be analyzed using data mining approaches combined with Internet-based technologies.
Interventions
None listed
Sponsors
The First Affiliated Hospital of Guangzhou Medical University
Guangzhou Science and Technology Innovation Commission,China
Guangzhou Institute of Respiratory Disease
Study design
Observational model
COHORT
Time perspective
PROSPECTIVE
Eligibility
Sex/Gender
ALL
Age
40 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* Patients was diagnosed as COPD according to Global Initiative for Chronic Obstructive Lung Disease (GOLD) guidelines older than 40 years old. * A signed and dated written informed consent is obtained prior to participation. * Able to comply with the requirements of the protocol and be available for study visits over 3 years.
Exclusion criteria
* A COPD subject will not be eligible for inclusion in this study if any of the following criteria apply: * Known respiratory disorders, or disorders identified at screening/visit 1 (including identification on the first CT scan), other than COPD (e.g.: lung cancer, sarcoidosis, tuberculosis, lung fibrosis, cystic fibrosis) * Known history of significant inflammatory disease, other than COPD (e.g. rheumatoid arthritis and Lupus) * Known to be severely alpha-1-antitrypsin deficient * Has experienced a moderate or severe exacerbation (requiring oral corticosteroid, antibiotics or hospitalisation) within the last 4 weeks * Having undergone lung surgery (e.g. lung reduction, lung transplant) * Have cancer or have had cancer in the 5 years prior to study entry * Having received a blood transfusion in the 4 weeks prior to study start * Inability to walk * Taking part in a blinded drug study * Having therapy with systemic corticosteroids at inclusion.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Establishment of prediction platform for COPD exacerbation | 3 years | The patients with chronic obstruction pulmonary disease will be followed up at intervals of 3 months for 3 years by the Modified British Medical Research Council (mMRC) score scale,spirometric analysis, sputum smear,questionnaire and so on. An exacerbation of COPD was diagnosed according to GOLD guidelines. Time to the first acute exacerbation and average number of acute exacerbations per year in COPD subjects will be record.Research of AECOPD Risk factors based on complex network analysis.Identification and validation of COPD exacerbations risk stratification and predictive markers based on data mining. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Developing new protein chips for AECOPD | 3 years | Systemic and airway autoantibody profiles and cytokine profiles will be measured using commercial multiplex bead-based assay to screen out a set of ideal AECOPD-related markers. |
| Detection of immune repertoire in COPD/AECOPD | 3 years | Immune status of COPD patients will be investigated by using the immune repertoire technique and its relationship with the pathophysiology of AECOPD will be identified. |
| Pathogenic microorganism and drug resistance monitoring for COPD exacerbation | 3 years | Dynamics of pathogenic microorganism and drug resistance in natural course of COPD will be investigated by using the metagenome technique and the culture technique. |
Countries
China
Outcome results
None listed