Intestinal Microbiota in COPD and Asthma

National Medical Research Center for Therapy and Preventive Medicine149 enrolled

Overview

The composition of the intestinal microbiota, the level of lipopolysaccharides, TMAO in the blood, and other parameters of patients with COPD (n=50), asthma (n=50) and the control (n=40) will be assessed as factors associated with exacerbations and respiratory symptoms in the prospective study (12 months).

The patients from "Biobank of blood and feces for the development of a clinical and biological platform as a basis for an innovative approach to the prevention of chronic non-infectious diseases based on the composition of the intestinal microbiota" study will be included (cross-sectional study). The protocol of the above study included the assessment of socio-demographic, anthropometric data, clinical blood pressure (BP), ECG, blood tests, fecal microbiota studies, spirometry data, diet questionnaire. ABPM, HBP, other questionnaires (mMRC, CAT, ACQ-5, GMBQ) will be added to initial data (=visit 1). Than the four visits (2-5th visits) in 3 each months will be performed to assess respiratory symptoms, exacerbations of COPD/asthma, respiratory infections, therapy, BP, and other parameters. The standard statistical methods will be used.

Study Type

OBSERVATIONAL

Enrollment

149

Conditions

Chronic Respiratory Diseases

Interventions

Identification of the composition of the intestinal microbiotaDIAGNOSTIC_TEST

Identification of the composition of the intestinal microbiota

Eligibility

Sex: ALLMin age: 18 YearsMax age: 74 YearsHealthy volunteers:

Medical Language ↔ Plain English

Inclusion Criteria: for control group: * Normal spirometry results with bronchodilation test (salbutamol 400 mcg); * Absence of COPD, asthma, chronic bronchitis and other lung diseases * BMI\<40kg/m2 for asthma/COPD groups: * Primary medical documentation confirming the diagnosis of COPD or asthma * Regular therapy for COPD, asthma and any chronic disease for at least 4 weeks prior to enrollment in this study. * FEV1 / FVC \<0.70 after inhalation of 400 mcg of salbutamol for patients with COPD * BMI\<40kg/m2 Exclusion Criteria: * Exacerbation of chronic noninfectious diseases, including exacerbation of COPD / asthma, within 4 weeks prior to enrollment in this study. * Exacerbation of COPD or asthma in the next 3 months, requiring the treatment of antibiotic therapy or systemic corticosteroids; * Cerebral stroke, transient ischemic attack or myocardial infarction within 6 months before the date of enrollment in the study; * Clinically significant chronic diseases (oncological, systemic diseases of the connective tissue, diseases of the blood system, heart failure, Crohn's disease, ulcerative colitis, etc. according to anamnesis); * GFR \<30 ml / min / 1.73m2; * Atopy in a patient with COPD or a control group (any allergic manifestations - skin, nasal, conjunctival, food, etc.); * Chronic respiratory diseases in a patient of the control group (COPD, asthma, chronic bronchitis, interstitial lung diseases); * History of organ transplantation; * Mental illness; * Intestinal infection (food poisoning) in the next 3 months; * Other acute infectious diseases. It is possible to turn on not earlier than 4 weeks after complete recovery and cessation of treatment; * History of severe COVID-19; * HIV infection, chronic viral hepatitis according to the history; * Clinically significant oncological disease; * Pregnancy and lactation; * Alcoholism, taking narcotic drugs; * Taking antimicrobial, probiotic drugs and systemic corticosteroids during the last 3 months; * Genetic engineering / biological therapy.

Locations (1)

NRCPM

Moscow, Russia

Outcomes

Primary Outcomes

Exacerbation of asthma / chronic obstructive pulmonary disease

Number of patients with exacerbation of bronchial asthma or chronic obstructive pulmonary disease, number of exacerbation per year

Time frame: 12 months

Data from ClinicalTrials.gov

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