Why the study?
It is currently impossible to predict frequent exacerbation phenotypes in COPD, and the specific association mechanism between lower respiratory tract and intestinal flora with AECOPD remains unclear.
Can metagenomic next-generation sequencing of lung and gut microbiota predict the frequency of acute exacerbations in patients with stable COPD?
Can metagenomic next-generation sequencing of lung and gut microbiota predict the frequency of acute exacerbations in patients with stable COPD?
This protocol outlines a prospective cohort study to explore the use of mNGS of lung and gut microbiota for predicting acute exacerbation frequency in patients with stable COPD.
Microbiota patterns may help identify frequent AECOPD phenotypes; hypothesis-generating and requires prospective validation before clinical use.
INTRODUCTION: Patients with frequent acute exacerbation phenotype chronic obstructive pulmonary disease (AECOPD) have a higher hospitalisation rate than infrequent exacerbation, the disease progresses quickly and treatment is more difficult. At present, it is impossible to predict patients with COPD with frequent acute exacerbation phenotypes. The composition of the lower respiratory tract flora and the intestinal flora is closely related to AECOPD, but the specific association mechanism between them is not very clear. This study used metagenomic next-generation sequencing (mNGS) technology to explore the microbial characteristics of the intestinal tract and airways of patients with COPD, and analyse the correlation between the sequencing results and inflammatory factors, immune factors and nutritional factors. METHODS AND ANALYSIS: This will be a prospective cohort study. We intend to recruit 152 patients with stable COPD. In the baseline, we will detect the participants' induced sputum and faecal flora through mNGS, and changes in blood immune levels, and the patient's condition is evaluated. Every 2 months, we will check the number of acute exacerbation through the phone range. After 12 months, we will check again the changes in the blood immune level, evaluate the patient's condition and count the number of episodes. ETHICS AND DISSEMINATION: This study has been approved by the ethics committee of Guangdong Provincial Hospital of Traditional Chinese Medicine (approval number ZF2019-219-03). The results of the study will be published in peer-reviewed journals. TRIAL REGISTRATION NUMBER: ClinicalTrials.gov Registry (ChiCTR2000032870).
No takes yet. Share an insight, caveat, or question.
Deng et al. (2021) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: