Risk Factors for Early Remodelling in Severe Asthma in Children (P'tit-ASTHME)
Primary Purpose
Asthma
Status
Completed
Phase
Not Applicable
Locations
France
Study Type
Interventional
Intervention
Fiberoptic bronchoscopy
Sponsored by

About this trial
This is an interventional diagnostic trial for Asthma
Eligibility Criteria
Inclusion Criteria:
Asthmatic children
- Parents (and possibly the child) who gave written informed consent.
- Affiliated with a social security scheme.
- Age from 1 to less than 5 years.
- Severe persistent asthma according to the criteria of the National Health Authority (Annex I) or NEW PROPOSED CRITERIA (adapted ATS (42)):
Major criteria (> 1) Asthma control in mild to moderate level requiring
- A continuous or semi continuous (≥ 50% of the year) by oral corticosteroids
- A treatment with high doses of inhaled corticosteroids (> 500 micrograms / day of Beclomethasone, or equivalent (> 400 micrograms / day of Budesonide,> 200 micrograms / day of Fluticasone) for at least 6 weeks.
And
minor criteria (> 2)
- The need for an additional daily treatment (β2-agonists, long-acting, theophylline, anti-leukotrienes)
- Symptoms that require taking daily or almost daily of β2-agonists of short action
- persistent obstruction (FEV <80% PEF variability> 20%) (If reliable spirometry, usually> 5 years of age)
- One or more seeking care in emergency / year
- At least three short courses of oral corticosteroids / year
- Rapid Increases caused by the decrease of 25% of the dose of oral corticosteroids or inhaled
- ATCD of severe acute asthma who put in life-threatening
Non-asthmatic children
Non asthmatic child with indication of endoscopy:
- Any endoscopy for a disease without acute or chronic inflammation in the biopsy area (≥1 to <5 years (1st part): congenital stridor, double aortic arch, foreign body removal inhaled, ...; ≥ 7 to ≤ 10 years ( 2nd component): inhaled foreign body removal, ...).
- Parents (and possibly the child) who gave written informed consent.
- Affiliated with a social security scheme.
Children not asthmatic postmortem (retrospective and prospective)
- Age from 1 to under 5 (1st part) or aged 7 to 10 years (2nd part) on the death
- Died without pulmonary pathology in the sampled area
Non asthmatic child with thoracic surgery:
- Age from 1 to under 5 (1st part) or aged 7 to 10 years (2nd part).
- Subject with pulmonary pathology, requiring thoracic surgery lobectomy, non-inflammatory in the sampled area.
- Parents (and possibly the child) who gave written informed consent.
- Affiliated with a social security scheme.
Exclusion Criteria:
Asthmatic children:
- Subject having a severe exacerbation of asthmatic disease requiring hospitalization in the 3 weeks preceding their inclusion.
- exclusion period on topic compared to another protocol.
- Subject with significant co-morbidity associated with asthma not of any nature whatsoever
- bronchial malformations (exclusion criterion ex post).
- Subject with a dental infection, or nasopharyngeal airway (viral or bacterial) with fever (> 39 ° C) in the 4 weeks preceding the survey.
- chronic viral infections (hepatitis, HIV).
- non-specific inclusion criteria to endoscopy:
- Review of hemostasis abnormal,
- Subject with a heart condition,
- Subject is not fasted for over 6 hours.
Children without asthma:
Non-asthmatic children with indication of endoscopy:
- asthma diagnosed by a doctor.
- exclusion period on topic compared to another protocol.
- Subject with significant co-morbidity associated with asthma not of any nature whatsoever.
- bronchial malformations (exclusion criterion ex post).
- Subject with a dental infection, or nasopharyngeal airway (viral or bacterial) with fever (> 39 ° C) in the 4 weeks preceding the survey.
- chronic viral infections (hepatitis, HIV).
- non-specific inclusion criteria to endoscopy:
- Review of hemostasis abnormal,
- Subject with a heart condition,
- Subject is not fasted for over 6 hours.
Children postmortem non-asthmatics:
- asthma diagnosed by a doctor.
- Subject with a dental infection, or nasopharyngeal airway (viral or bacterial) with fever (> 39 ° C) within 4 weeks before sampling of tissue.
- chronic viral infections (hepatitis, HIV).
Non-asthmatic children with thoracic surgery:
- asthma diagnosed by a doctor.
- exclusion period on topic compared to another protocol.
- Subject with a dental infection, or nasopharyngeal airway (viral or bacterial) with fever (> 39 ° C) within 4 weeks before sampling of tissue.
- chronic viral infections (hepatitis, HIV).
Sites / Locations
- CHU de Bordeaux
- Hôpital des Enfants
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Sham Comparator
Arm Label
Asthmatic children
Non-asthmatic children
Arm Description
Outcomes
Primary Outcome Measures
Evaluation of Airway remodeling (distance from the reticular membrane to the smooth muscle).
Secondary Outcome Measures
Full Information
NCT ID
NCT02806466
First Posted
June 15, 2016
Last Updated
June 15, 2016
Sponsor
University Hospital, Bordeaux
1. Study Identification
Unique Protocol Identification Number
NCT02806466
Brief Title
Risk Factors for Early Remodelling in Severe Asthma in Children
Acronym
P'tit-ASTHME
Official Title
Risk Factors for Early Remodelling in Severe Asthma in Children
Study Type
Interventional
2. Study Status
Record Verification Date
June 2016
Overall Recruitment Status
Completed
Study Start Date
March 2012 (undefined)
Primary Completion Date
November 2015 (Actual)
Study Completion Date
November 2015 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University Hospital, Bordeaux
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
Background: Asthma is a frequent disease characterized by bronchial hyperresponsiveness, inflammation and remodeling. Consistent epidemiological data indicate that outcome of asthma in adults may be determined in early childhood. This may be due to bronchial remodeling, an abnormal repair process that contributes to the development of poorly reversible airway narrowing. It appears very early in the natural history of the disease and involves increased mass of bronchial smooth muscle (BSM). The mechanism of such an increase has been related with an increase in smooth muscle cell proliferation. Recently, we have demonstrated that in severe asthma, BSM increased proliferation is induced by an enhanced mitochondrial biogenesis. Moreover, we have also shown that immature human, non-asthmatic airway smooth muscle cells (ASMC) proliferate to a greater extent than normal adult ASMC, in a similar fashion to adult asthmatic ASMC. Immature ASMC may thus have great potential to stimulate airway remodeling. We thus hypothesized that remodeling is an early process and certain characteristics of ASMC in severe preschool asthma may predispose such children to persistent remodeling with airway obstruction later in life.
Purpose: To investigate prognostic factors of airway remodeling in preschool children, with special attention to ASMC proliferation (mitochondrial mass & biogenesis).
Methods: In the initial phase of the project, 75 severe asthmatic preschool children (<5 yr) will be prospectively recruited from the "CHU de Bordeaux" and the "CHU de Toulouse" according to the "Haute Autorité de Santé" criteria. Inclusion visit will include written informed consent, asthma control evaluation, clinical examination, lung function testing (exhaled NO, plethysmography), prick tests, chest X Ray and blood sample for total IgE levels. Bronchial specimens from all subjects will be obtained by fiberoptic bronchoscopy at visit 2. Airway remodeling will be evaluated by morphological analysis. After smooth muscle mitochondria will be analyzed by electronic microscopy & immunoblotting. Comparison between the 2 groups will be performed by unpaired t tests for parametric data and x2-tests for non-parametric data. In the second phase of the project, patients will then be followed-up till the age of 7-10 yrs, when another bronchoscopy with biopsies will be performed.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Asthma
7. Study Design
Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
67 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Asthmatic children
Arm Type
Active Comparator
Arm Title
Non-asthmatic children
Arm Type
Sham Comparator
Intervention Type
Procedure
Intervention Name(s)
Fiberoptic bronchoscopy
Primary Outcome Measure Information:
Title
Evaluation of Airway remodeling (distance from the reticular membrane to the smooth muscle).
Time Frame
1 day
10. Eligibility
Sex
All
Minimum Age & Unit of Time
1 Year
Maximum Age & Unit of Time
5 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Asthmatic children
Parents (and possibly the child) who gave written informed consent.
Affiliated with a social security scheme.
Age from 1 to less than 5 years.
Severe persistent asthma according to the criteria of the National Health Authority (Annex I) or NEW PROPOSED CRITERIA (adapted ATS (42)):
Major criteria (> 1) Asthma control in mild to moderate level requiring
A continuous or semi continuous (≥ 50% of the year) by oral corticosteroids
A treatment with high doses of inhaled corticosteroids (> 500 micrograms / day of Beclomethasone, or equivalent (> 400 micrograms / day of Budesonide,> 200 micrograms / day of Fluticasone) for at least 6 weeks.
And
minor criteria (> 2)
The need for an additional daily treatment (β2-agonists, long-acting, theophylline, anti-leukotrienes)
Symptoms that require taking daily or almost daily of β2-agonists of short action
persistent obstruction (FEV <80% PEF variability> 20%) (If reliable spirometry, usually> 5 years of age)
One or more seeking care in emergency / year
At least three short courses of oral corticosteroids / year
Rapid Increases caused by the decrease of 25% of the dose of oral corticosteroids or inhaled
ATCD of severe acute asthma who put in life-threatening
Non-asthmatic children
Non asthmatic child with indication of endoscopy:
Any endoscopy for a disease without acute or chronic inflammation in the biopsy area (≥1 to <5 years (1st part): congenital stridor, double aortic arch, foreign body removal inhaled, ...; ≥ 7 to ≤ 10 years ( 2nd component): inhaled foreign body removal, ...).
Parents (and possibly the child) who gave written informed consent.
Affiliated with a social security scheme.
Children not asthmatic postmortem (retrospective and prospective)
Age from 1 to under 5 (1st part) or aged 7 to 10 years (2nd part) on the death
Died without pulmonary pathology in the sampled area
Non asthmatic child with thoracic surgery:
Age from 1 to under 5 (1st part) or aged 7 to 10 years (2nd part).
Subject with pulmonary pathology, requiring thoracic surgery lobectomy, non-inflammatory in the sampled area.
Parents (and possibly the child) who gave written informed consent.
Affiliated with a social security scheme.
Exclusion Criteria:
Asthmatic children:
Subject having a severe exacerbation of asthmatic disease requiring hospitalization in the 3 weeks preceding their inclusion.
exclusion period on topic compared to another protocol.
Subject with significant co-morbidity associated with asthma not of any nature whatsoever
bronchial malformations (exclusion criterion ex post).
Subject with a dental infection, or nasopharyngeal airway (viral or bacterial) with fever (> 39 ° C) in the 4 weeks preceding the survey.
chronic viral infections (hepatitis, HIV).
non-specific inclusion criteria to endoscopy:
Review of hemostasis abnormal,
Subject with a heart condition,
Subject is not fasted for over 6 hours.
Children without asthma:
Non-asthmatic children with indication of endoscopy:
asthma diagnosed by a doctor.
exclusion period on topic compared to another protocol.
Subject with significant co-morbidity associated with asthma not of any nature whatsoever.
bronchial malformations (exclusion criterion ex post).
Subject with a dental infection, or nasopharyngeal airway (viral or bacterial) with fever (> 39 ° C) in the 4 weeks preceding the survey.
chronic viral infections (hepatitis, HIV).
non-specific inclusion criteria to endoscopy:
Review of hemostasis abnormal,
Subject with a heart condition,
Subject is not fasted for over 6 hours.
Children postmortem non-asthmatics:
asthma diagnosed by a doctor.
Subject with a dental infection, or nasopharyngeal airway (viral or bacterial) with fever (> 39 ° C) within 4 weeks before sampling of tissue.
chronic viral infections (hepatitis, HIV).
Non-asthmatic children with thoracic surgery:
asthma diagnosed by a doctor.
exclusion period on topic compared to another protocol.
Subject with a dental infection, or nasopharyngeal airway (viral or bacterial) with fever (> 39 ° C) within 4 weeks before sampling of tissue.
chronic viral infections (hepatitis, HIV).
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
MICHAEL FAYON, Professor
Organizational Affiliation
University Hospital, Bordeaux
Official's Role
Principal Investigator
Facility Information:
Facility Name
CHU de Bordeaux
City
Bordeaux
State/Province
Aquitaine
ZIP/Postal Code
33000
Country
France
Facility Name
Hôpital des Enfants
City
Toulouse
State/Province
Languedoc-Roussillon-Midi-Pyrénées
ZIP/Postal Code
31026
Country
France
12. IPD Sharing Statement
Plan to Share IPD
No
Learn more about this trial
Risk Factors for Early Remodelling in Severe Asthma in Children
We'll reach out to this number within 24 hrs