This study is aiming at explore the characteristics of intestinal microbiome during the early progression of COPD, the correlation between the changes of intestinal microbiome and the severity and risk of acute exacerbation of COPD, the correlation between microbial metabolites SCFA and immune function of COPD. Then reveal the influence of intestinal microecology on the development of COPD and the possible mechanism of intestinal microecology in the pathogenesis of COPD.
1. Invite participants according to inclusion criteria and exclusion criteria and divide them into 4 groups, including healthy control (HC), high-risk COPD group (HG), early COPD group (EG), mild and moderate COPD group (MG). Research contents will be explained detailedly to the participants, and the healthy participants and COPD patients who volunteer to participate in this study will sign the informed consent form (ICF) under the premise of adequate understanding. 2. Collect clinical data of the participants and asses the severity of symptoms and the risk of acute exacerbation of COPD patients. Clinical data include general condition, history of past illness, history of present illness, personal history, family history and the examination results of blood routine, pulmonary function and compatible computed tomography. Breathlessness measurement adopt the modified British Medical Reseach Council (mMRC); symptoms measurement adopt COPD assessment test (CAT); quality of life measurement adopt St. George's Respiratory Questionnaire (SGRQ); risk of acute exacerbation measurement adopt dyspnea,degree of airflow obstruction,smoking status and the number of exacerbation (DOSE) scoring system. 3. Collect fecal specimens from the participants on the morning of the same day. During the first three days of collection, they should keep their daily dietary habits and avoid sudden changes in dietary habits. Considerations: first remove the urine, excrement into a clean dry container, do not mix with urine and other sundries; the part of the feces that do not contact the air and container is taken from the specimen; women who are menstruating cannot be sampled. Each participant collect 3 fecal samples with a sterile spoon in a sterile enzyme-free cryopreservation tube, label the sample name and date, quickly placed in a -20℃ refrigerator, and transported to the hospital within 2 hours, where they were stored at -80℃. Fecal microbiome are detected by 16S rRNA gene sequencing and metabolite short chain fatty acid (SCFA) are detected by Gaschromatography (GC). 4. Serum of participants are collected at the clinical laboratory and detect indicators related to immune function by enzyme-linked immunosorbent assay (ELISA). 5. Explore the characteristics of intestinal microbiome during the early progression of COPD, the correlation between the changes of intestinal microbiome and the severity and risk of acute exacerbation of COPD, the correlation between microbial metabolites SCFA and immune function of COPD.
Second Affiliated Hospital of Xi'an Jiaotong University
Xi'an, Shaanxi, China
Breathlessness measurement
modified British Medical Reseach Council (mMRC):the score increases from 0 to 4,and higher scores mean a heavier symptom.
Time frame: 1 month
Symptoms measurement
COPD assessment test (CAT):the score increases from 0 to 40,and higher scores mean a heavier symptom.
Time frame: 1 month
Quality of life measurement
St. George's Respiratory Questionnaire (SGRQ): the score increases from 0 to 100,and higher scores mean a heavier symptom.
Time frame: 1 month
Risk of acute exacerbation of participants
dyspnea,degree of airflow obstruction,smoking status,the number of exacerbation (DOSE): the score increases from 0 to 9,and higher scores mean a higher risk of acute exacerbation.
Time frame: 1 month
Pulmonary function
Forced expiratory volume in 1 s (FEV1)/forced vital capacity (FVC), FEV1%predicted, MMEF25-75%: range from 0%-100%, and higher percentages mean a heavier symptom.
Time frame: 1 month
Compatible computed tomography
mean lung density
Time frame: 1 month
Characteristics of intestinal microbiome
Alpha diversity,Beta diversity,Species differences between groups at different taxonomic levels.
Time frame: 1 month
Contents of short chain fatty acid in fecal samples
acetic acid, propionic acid, butyric acid
Time frame: 1 month
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.
Study Type
OBSERVATIONAL
Enrollment
120
Blood routine
neutrophilic granulocyte percent, eosinophilic granulocyte percent: higher percentages mean a heavier symptom.
Time frame: 1 month
Concentration of protein in serum
fibrinogen, C-reactive protein, surfactant protein-D(SP-D)
Time frame: 1 month
Concentration of enzyme in serum
neutrophil elastase, alpha1-antitrypsin
Time frame: 1 month
Concentration of inflammatory factor in serum
TNF-α, IFN-γ, IL-6, IL-8, IL-17
Time frame: 1 month
Concentration of chemokine in serum
CCL-16, CCL-18
Time frame: 1 month