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This study aims to investigate the clinical characteristics and heterogeneities of early chronic obstructive pulmonary disease (COPD), to determine the disease development of early COPD, and to establish a multidimensional model for predicting the outcomes of early COPD.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Preserved ratio impaired spirometry (PRISm) | People with post-bronchodilator forced expiratory volume in one second (FEV1)/forced vital capacity (FVC) ≥ 0.70 and FEV1 and/or FVC < 80% predicted, or FEV1/FVC ≥ lower limit of normal (LLN) and FEV1 < LLN. | ||
| COPD Stage 0 | People who had COPD-related risk factor exposure (e.g. cigarette smoke) and/or presented with respiratory symptoms (e.g. chronic cough, and/or sputum production) whereas with normal pulmonary function. | ||
| Pre-COPD | People (importantly, of any age) who had respiratory symptoms (e.g. cough, sputum production, dyspnea, and/or exacerbation) with or without detectable structural (e.g. thoracic computed tomography (CT) emphysema, small and/or large airway impairments) and/or functional (e.g. low diffusion capacity for carbon monoxide (DLCO), hyperinflation, small airway obstruction, and/or accelerated FEV1 decline) abnormalities, in the absence of airflow limitation, and who might (or not) develop persistent airflow limitation (i.e. COPD) over time. | ||
| Early COPD | People who were younger than 50 years with ten or more pack-years smoking history and any of these abnormalities: i) early airflow limitation (post-bronchodilator FEV1/FVC < LLN), ii) compatible thoracic CT abnormalities, iii) rapid decline in FEV1 (> 60 ml/year) that was accelerated relative to FVC. | ||
| Young COPD | COPD patients with post-bronchodilator FEV1/FVC < 0.70 diagnosed in the 20-50 year age range. |
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| Measure | Description | Time Frame |
|---|---|---|
| Number of participants with COPD exacerbation | COPD exacerbation refers to acute deterioration of respiratory symptoms (e.g. cough, sputum, wheeze, dyspnea), especially resulting in hospital visit or admission. | One year |
| Measure | Description | Time Frame |
|---|---|---|
| FEV1 | One year | |
| FVC | One year | |
| FEV1/FVC ratio |
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Inclusion Criteria:
Exclusion Criteria:
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This study plans to involve the individuals with different early COPD status, as well as comparable controls.
| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Jieping Lei, Ph.D. | Contact | +86 010 8420 6408 | jiepinglei@126.com |
| Name | Affiliation | Role |
|---|---|---|
| Jieping Lei, Ph.D. | China-Japan Friendship Hospital | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| China-Japan Friendship Hospital | Recruiting | Beijing | Beijing Municipality | 100029 | China |
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| ID | Term |
|---|---|
| D029424 | Pulmonary Disease, Chronic Obstructive |
| ID | Term |
|---|---|
| D008173 | Lung Diseases, Obstructive |
| D008171 | Lung Diseases |
| D012140 | Respiratory Tract Diseases |
| D002908 | Chronic Disease |
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Peripheral blood sample
| Mild COPD | COPD patients with post-bronchodilator FEV1/FVC < 0.70 and FEV1 ≥ 80% predicted. |
| Controls | People who were not belonged to any of above six early COPD status, and with pre- and post-bronchodilator FEV1/FVC ≥ 0·70, and with post-bronchodilator FEV1/FVC ≥ LLN. |
| One year |
| FEV1% predicted value | One year |
| FVC% predicted value | One year |
| The COPD Assessment Test scale | The COPD Assessment Test scores range from 0 to 40, with higher scores indicating worse symptoms. | One year |
| The modified Medical Research Council dyspnea scale | The modified Medical Research Council dyspnea scores range from 0 to 4, with higher scores indicating more severe dyspnea. | One year |
| D020969 |
| Disease Attributes |
| D010335 | Pathologic Processes |
| D013568 | Pathological Conditions, Signs and Symptoms |