Chronic Respiratory Diseases
Conditions
Keywords
chronic respiratory diseases phenotyping
Brief summary
World Health Organization (WHO) considers chronic respiratory disease (CRD) as one of its four priorities. These diseases include asthma and rhinitis, chronic obstructive pulmonary diseases (COPD), occupational lung diseases, sleep apnoea syndromes, pulmonary hypertension, bronchiectasis and interstitial lung diseases. They constitute a serious public health problem in all countries throughout the world, in particular in low and middle income countries and in deprived populations. Hundreds of millions of people of all ages, in all countries of the world, are affected by chronic respiratory diseases. More than 50% of them live in low and middle income countries. Over 90% of deaths and the complete inability, due to CRDs occur in countries with low or middle incomes. The main causes of CRD are: tobacco smoke, occupational factors, indoor air pollution and outdoor air pollution, allergens, sequelae of respiratory infections such as tuberculosis. More than 30% of the population of Ho Chi Minh City (HCMC) could develop a CRD. In fact, 15% of children and 7% of adults could become asthma and 6% of the population could become COPD due to smoking. Children exposed to fumes from biomass burning, early in their life, seem to have a higher risk to develop COPD. The high level of air pollution in HCMC could aggravate asthma / COPD. Populations combining the rural risk (exposure to smoke from biomass) and the urban risk (smoking, pollution) may develop COPD much earlier (before age 40). Among the 9 million people in HCMC, 50% of the population is rural origin. Within this population, parasites could play a protective role against the risk of allergic asthma and consequently, the better control of helminthiasis among urban population, may result in allergic diseases such as asthma and anaphylaxis. Finally, the sequelae of tuberculosis (incidence is 200/100000) could participate to the morbidity of COPD / CRD. Study granted by the ARES-CUD (Comission universitaire au développement)
Interventions
OTHERepidemiology
Relative prevalence of different chronic respiratory disease phenotypes
Sponsors
Brugmann University Hospital
Study design
Time perspective
CROSS_SECTIONAL
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* Age: ≥ 18 years old * Gender: Female and Male * Signed informed consent * Out-patients at the Pham Ngoc Thach Hospital * One or several symptoms suggesting chronic respiratory disease (cough, chest tightness, wheezing, dyspnoea, sputum), lasting 3 months or more. * Lung function defect (FEV1/FVC \< 0,7 or FEV1 \< 80% PV with FEV1/FVC \> 0,7 or FEV1\> 80% PV and FEV1/FVC \> 0,7 with a decrease of DLCO (\< 80% PV). FEV1: Forced Expiratory Volume in 1 Second FVC : Forced Vital Capacity PV: predicted value DLCO: Diffusing Capacity of the Lung for Carbon Monoxide * Patients are able to stop anti-histamine 5 days before evaluation. * Patients are able to stop bronchodilator treatment before performing lung function test according to standard practice (immediate release theophylline: 24 hours, long acting β2-agonist: 12 hours, short acting β2-agonist: 6 hours and short acting anticholinergic: 8 hours).
Exclusion criteria
* The patients do not agree to participate in the study. * Presence of one or more chronic diseases: HIV, active tuberculosis, hypertension, heart failure, diabetes, low BMI (\<18.5) or mental health disorders. * Treatment with B-blockers, drugs of vascular/heart disease
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Relative prevalence of the different chronic respiratory diseases phenotype | 4 months after start of study | This will be measured by the percentage of each chronic respiratory diseases phenotype, according to the lung function test. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| role of occupational risk factors in developing chronic respiratory diseases | 4 months after start of study | This will be measured by means of a questionnaire. |
| role of clinical risk factors in developing chronic respiratory diseases | 4 months after start of study | This will be measured by means of a questionnaire and lung function test |
| role of environmental risk factors in developing chronic respiratory diseases | 4 months after start of study | This will be measured by means of a questionnaire. |
| Induced sputum analysis to assess the relationship between phenotype and endotype among a sub-group of chronic respiratory diseases | 4 months after start of study | — |
| Biomarkers assessment for risk factors of chronic respiratory diseases | 4 months after start of study | Total IgE number and specific IgE number if needed depending on each phenotype of chronic respiratory disease |
| Allergen skin reactivity test to assess the role of atopic in developing chronic respiratory diseases | 4 months after start of study | — |
Countries
Vietnam
Outcome results
None listed