Asthma, Bronchial
Conditions
Brief summary
The study is to establish a standardized asthma cohort study, build an information network platform system and a biospecimen bank for asthma cohort, establish clear follow-up standards and norms, observe the asthma outcomes and identify biomarkers to predict asthma outcomes.
Detailed description
This is a single center observational prospective longitudinal cohort study to establish a standardized asthma cohort, consisting of 400 patients with asthma. Baseline data including lung function test, chest CT, induced sputum, etc. was collected and the patients were followed up for 2 or more years. Subjects who met the 2023 GINA diagnostic criteria for asthma and were able to participate in the study according to the protocol and sign the informed consent were included. No additional investigational drugs will be applied to the patients. Blood samples are transported to designated laboratories for safekeeping and biomarker testing. We aimed to explore the mechanism of biomarkers involved in asthma pathogenesis and identify treatable traits related to disease outcome. Full analysis set will be used for all analyses. Missing data will be analyzed as it is. Statistical analysis will be conducted by epidemiology & statistics work group from Chinese Academy of Sciences, using SAS and SUDAAN software. An electronic data capture system will be used in this study. Paper-based questionnaire administration will also be used. Questionnaire variables will be checked before data entry. During the study, PI will be in charge of the monitoring of the whole procedure. Working group will do the data cleaning and data analyzing.
Interventions
DIAGNOSTIC_TESTDiagnostic Test: lung function test, chest CT, induced sputum, blood routine test, IgE test, FeNO test, six minutes walk test, questionnaires for asthma
lung function test, chest CT, induced sputum, blood routine test, IgE test, FeNO test, six minutes walk test, questionnaires for asthma were performed. All interventions was made according to routine diagnosis and treatment.
Sponsors
Beijing Chao Yang Hospital
Study design
Observational model
COHORT
Time perspective
PROSPECTIVE
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* Age \>18 * Meet the 2023 edition of GINA asthma diagnostic criteria * Subjects must sign informed consent prior to study participation, participate in the study according to the protocol and follow up for 2 years
Exclusion criteria
* Suffering from other massive lung tissue destructive diseases such as severe bronchiectasis and tuberculosis * Severe pleural disease and/or sternal and rib lesions * Serious uncontrolled disease of other system * Thoracic or abdominal surgery in the past 3 months * Eye surgery in the past three months * Retina detachment * Myocardial infarction within the last 3 months * Hospitalized for heart disease within the past 3 months * Ongoing anti-tuberculosis treatment * Pregnancy or breast feeding
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Asthma Control Test(ACT) | 2 years | As)thma control was assessed by Asthma Control Test(ACT) |
| Asthma Control Questionnaire(ACQ) | 2 years | sthma control was assessed by Asthma Control Questionnaire(ACQ) |
| Induced sputum analysis | 2 years | Identification of asthma endotypes was based on Induced sputum analysis |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Prognosis prediction of asthma with specific treatment regimen | 2 years | Prognosis prediction of asthma with specific treatment regimen was based on different phenotypes and biomarkers |
Countries
China
Contacts
Primary ContactMeishan Liu, M.D.
Backup ContactYing Wang, M.D.
Outcome results
None listed