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Analysis of Bronchial Remodeling Using Resonance Magnetic Imaging in Severe Asthmatic childrEn (ARISE)

Primary Purpose

Asthma in Children

Status
Recruiting
Phase
Not Applicable
Locations
France
Study Type
Interventional
Intervention
bronchial biopsies
Sponsored by
University Hospital, Bordeaux
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for Asthma in Children focused on measuring asthma, children, serious, magnetic resonance imaging

Eligibility Criteria

6 Years - 17 Years (Child)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Child from 6 to 17 years old
  • Having informed consent signed by the holders of parental authority.
  • Having a diagnosis of severe asthma according to the Global Initiative for Asthma (GINA) 2020;

    • Asthma: chronic inflammatory disease of the airways, defined mainly by respiratory symptoms such as wheezing, dyspnea, chest tightness and / or cough, which may vary in time and intensity associated with a limitation also varying in the time of expiratory flow.
    • Severe asthma: asthma which requires treatment with inhaled corticosteroids in high doses plus a second long-acting bronchodilator type controller, to maintain control of symptoms and / or whose control worsens if this treatment is reduced and / or which remains uncontrolled despite this treatment.
  • Having to carry out as part of the current care a functional respiratory exploration;
  • Should require as part of the routine care of a bronchial fibroscopy.

Exclusion Criteria:

  • Patient without affiliation or not benefiting from a social security scheme;
  • Patient being in a period of relative exclusion from another protocol;
  • Patient born before 36 weeks of amenorrhea;
  • Patient with a documented history of pulmonary fibrosis, primary pulmonary arterial hypertension, cystic fibrosis, pulmonary malformation or chronic viral infections (hepatitis, HIV);
  • Patient presenting with an exacerbation of asthma requiring systemic corticosteroids within the previous 4 weeks;
  • Patient with any dental, nasopharyngeal or bronchial infection with fever (> 39 ° C) requiring systemic antibiotics within the previous 4 weeks
  • Patient with a contraindication to MRI:

    • Abdominal perimeter greater than 200 cm;
    • Claustrophobia or inability to lie still for 12 minutes;
    • Have a pacemaker or implantable defibrillator, intraocular metallic foreign body, intracranial metal clip, a pre-6000 Starr-Edwards type heart valve prosthesis, or a biomedical device such as an insulin pump or neurostimulator, cochlear implant and metal patch.
  • Patient with a contraindication to anesthesia;
  • Patient with a contraindication to bronchial fibroscopy following:

    • Abnormal hemostasis assessment;
    • Subject with cardiac pathology.

Sites / Locations

  • CHU de Bordeaux - Explorations FonctionnellesRecruiting
  • Centre Hospitalier de Saintonge

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

lung MRI

Arm Description

The procedure under study is lung MRI, performed on a 1.5T magnet (AERA dot 1.5T, Siemens), without anesthesia and without injection or inhalation of contrast agent.

Outcomes

Primary Outcome Measures

Measure of Bronchial thickness (BT) in UTE-T1 (in mm)
Mean (or median if the distribution is not normal) of the following candidate parameters measured on the 3D-UTE MRI performed either on the average of the 4th bronchial generation or on the only biopsied bronchus obtained at Visit 3: - Bronchial thickness (BT) in UTE-T1 (mm)
Measure of Signal strength of the bronchial wall (SB) in UTE-T1 (in milliseconds)
Mean (or median if the distribution is not normal) of the following candidate parameters measured on the 3D-UTE MRI performed either on the average of the 4th bronchial generation or on the only biopsied bronchus obtained at Visit 3: - Signal intensity of bronchial edema (SE) in T2- Turbo Spin-Echo (TSE) (second)
Measure of Volume of bronchial edema (VO) in T2-Turbo Spin-Echo (TSE) (in cubic millimeters)
Mean (or median if the distribution is not normal) of the following candidate parameters measured on the 3D-UTE MRI performed either on the average of the 4th bronchial generation or on the only biopsied bronchus obtained at Visit 3: - Volume of bronchial edema (VE) in T2-Turbo Spin-Echo (TSE) (mm^3)
Measure of Bronchial edema (SO) signal intensity in T2-Turbo Spin-Echo (TSE) (in milliseconds)
Mean (or median if the distribution is not normal) of the following candidate parameters measured on the 3D-UTE MRI performed either on the average of the 4th bronchial generation or on the only biopsied bronchus obtained at Visit 3: - Signal intensity of bronchial edema (SE) in T2-Turbo Spin-Echo (TSE) (second)

Secondary Outcome Measures

Comparison each measurable values between 2 Physicians evaluated in the principal outcome measures
Intra-and inter-observer intraclass correlation coefficients of each of the parameters measured in 3D-UTE MRI, with their 95% confidence interval, and graphic representation of Bland and Altman
Measure of expiratory forced vital capacity (FVC)
Functional respiratory data
Measure of forced expiratory volume in one second (FEV1)
Functional respiratory data
Measure length of reticular basement membrane (RBM) completely denuded or covered by a single layer of basal cells with no intact ciliated or goblet cell over total basement membrane length
Values measured by immunohistochemistry to assess epithelial integrity in percent.
Measure of reticular basement membrane thickness (µm)
Values measured by immunohistochemistry
Measure of density of blood vessels (number/cm²)
Values measured by immunohistochemistry
Measure of normalized fibrosis area (%)
Values measured by immunohistochemistry
Measure of reticular basement membrane to bronchial smooth muscle distance (µm)
Values measured by immunohistochemistry

Full Information

First Posted
May 11, 2022
Last Updated
June 8, 2023
Sponsor
University Hospital, Bordeaux
Collaborators
Institut National de la Santé Et de la Recherche Médicale, France
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1. Study Identification

Unique Protocol Identification Number
NCT05419622
Brief Title
Analysis of Bronchial Remodeling Using Resonance Magnetic Imaging in Severe Asthmatic childrEn
Acronym
ARISE
Official Title
Analysis of Bronchial Remodeling Using Resonance Magnetic Imaging in Severe Asthmatic childrEn
Study Type
Interventional

2. Study Status

Record Verification Date
June 2023
Overall Recruitment Status
Recruiting
Study Start Date
June 8, 2023 (Actual)
Primary Completion Date
June 30, 2025 (Anticipated)
Study Completion Date
August 30, 2025 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University Hospital, Bordeaux
Collaborators
Institut National de la Santé Et de la Recherche Médicale, France

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
This study is a diagnostic imaging pilot study evaluating performance of 3D-Ultrashort Time Echo (3D-UTE) Magnetic Resonance Imaging (MRI) for the diagnosis of bronchial remodeling in children with severe asthma. The primary objective is to compare bronchial parameters measured by 3D-UTE MRI according to the presence or the absence of bronchial remodeling determined on bronchial biopsies using immunohistochemistry, in severe asthmatic children.
Detailed Description
Background: Asthma is the most frequent chronic disease in childhood. Severe asthma accounts for only 5% of patients but more than half of the costs of the disease. It is characterized by bronchial remodeling, including an increase in bronchial smooth muscle (BSM) mass associated with an increase in bronchial smooth muscle cell proliferation. This increased cell proliferation has been related with an abnormal calcium homeostasis and an enhanced mitochondrial biogenesis. Moreover, the release of growth factors by inflammatory cells and bronchial epithelial cells reinforces BSM cell proliferation. BSM remodeling is correlated with the severity and poor control of the disease. In children, bronchial remodeling could be assessed by performing endobronchial biopsies during bronchoscopy. However, this method is invasive and cannot be repeated to follow the remodeling. Non-invasive quantification of proximal bronchial thickness by computed tomography (CT) has been demonstrated. However, CT was unable to differentiate bronchial inflammation from remodeling on the one hand, and, on the other hand, CT is a radiating examination, and the repetition of X-ray exposures can be a source of cancer. Recently, the team evaluated at the university hospital of Bordeaux new MRI sequences to obtain 3D high-resolution images (3D-UTE), close to that of CT. This 3D-UTE has the advantage of being performed without any injection or inhalation of contrast medium and non-irradiating. Moreover, MRI provides additional data on signal intensity or bronchial inflammation that is not accessible on CT imaging. However, to the best of our knowledge, the use of 3D -UTE high resolution MRI has not been demonstrated in a pediatric population with severe asthma. Purpose: To compare bronchial parameters measured in 3D-UTE MRI according to the presence or not of bronchial remodeling measured by immunohistochemistry on bronchial biopsies obtained from severe asthmatic children. Methods: The investigator's team therefore wishes to carry out pulmonary MRI without anesthesia, nor injection nor inhalation of contrast product in severe asthmatic children. Two sequences in axial cuts will be performed for a total duration of 12 minutes (6 minutes by sequence). Bronchial quantitative data obtained by MRI will be compared to those obtained from immunohistochemical analysis of bronchial biopsies performed during bronchoscopy. Severe asthmatic children requiring bronchoscopy will be identified during consultation or hospitalization relative of the disease. The inclusion visit (V1) will be performed during a consultation for asthma of the usual care of the child. Then, the second visit (V2) will correspond to the anesthesia consultation of the usual care of the child to check the absence of contraindications to anesthesia and bronchoscopy. The third visit (V3) will correspond to the pulmonary MRI and flexible bronchoscopy. According to the classic procedure, bronchoscopy will be performed during a hospitalization. The pulmonary MRI, as well as blood tests and lung function testing, will be performed at the beginning of the hospitalization, the day before the bronchoscopy. Children will be monitored 24 hours in hospitalization after the bronchoscopy.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Asthma in Children
Keywords
asthma, children, serious, magnetic resonance imaging

7. Study Design

Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Model Description
Early study to evaluate the diagnostic and diagnostic performances of an imaging sequence, non-randomized, observational, prospective and bicentric.
Masking
None (Open Label)
Allocation
N/A
Enrollment
100 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
lung MRI
Arm Type
Experimental
Arm Description
The procedure under study is lung MRI, performed on a 1.5T magnet (AERA dot 1.5T, Siemens), without anesthesia and without injection or inhalation of contrast agent.
Intervention Type
Biological
Intervention Name(s)
bronchial biopsies
Intervention Description
This fibroscopy will make it possible to perform 4 bronchial biopsies at the level of the 4th bronchial generation (subsegmental bronchi), using suitable pediatric forceps.
Primary Outcome Measure Information:
Title
Measure of Bronchial thickness (BT) in UTE-T1 (in mm)
Description
Mean (or median if the distribution is not normal) of the following candidate parameters measured on the 3D-UTE MRI performed either on the average of the 4th bronchial generation or on the only biopsied bronchus obtained at Visit 3: - Bronchial thickness (BT) in UTE-T1 (mm)
Time Frame
Day 30
Title
Measure of Signal strength of the bronchial wall (SB) in UTE-T1 (in milliseconds)
Description
Mean (or median if the distribution is not normal) of the following candidate parameters measured on the 3D-UTE MRI performed either on the average of the 4th bronchial generation or on the only biopsied bronchus obtained at Visit 3: - Signal intensity of bronchial edema (SE) in T2- Turbo Spin-Echo (TSE) (second)
Time Frame
Day 30
Title
Measure of Volume of bronchial edema (VO) in T2-Turbo Spin-Echo (TSE) (in cubic millimeters)
Description
Mean (or median if the distribution is not normal) of the following candidate parameters measured on the 3D-UTE MRI performed either on the average of the 4th bronchial generation or on the only biopsied bronchus obtained at Visit 3: - Volume of bronchial edema (VE) in T2-Turbo Spin-Echo (TSE) (mm^3)
Time Frame
Day 30
Title
Measure of Bronchial edema (SO) signal intensity in T2-Turbo Spin-Echo (TSE) (in milliseconds)
Description
Mean (or median if the distribution is not normal) of the following candidate parameters measured on the 3D-UTE MRI performed either on the average of the 4th bronchial generation or on the only biopsied bronchus obtained at Visit 3: - Signal intensity of bronchial edema (SE) in T2-Turbo Spin-Echo (TSE) (second)
Time Frame
Day 30
Secondary Outcome Measure Information:
Title
Comparison each measurable values between 2 Physicians evaluated in the principal outcome measures
Description
Intra-and inter-observer intraclass correlation coefficients of each of the parameters measured in 3D-UTE MRI, with their 95% confidence interval, and graphic representation of Bland and Altman
Time Frame
Day 30
Title
Measure of expiratory forced vital capacity (FVC)
Description
Functional respiratory data
Time Frame
Day 30
Title
Measure of forced expiratory volume in one second (FEV1)
Description
Functional respiratory data
Time Frame
Day 30
Title
Measure length of reticular basement membrane (RBM) completely denuded or covered by a single layer of basal cells with no intact ciliated or goblet cell over total basement membrane length
Description
Values measured by immunohistochemistry to assess epithelial integrity in percent.
Time Frame
Day 30
Title
Measure of reticular basement membrane thickness (µm)
Description
Values measured by immunohistochemistry
Time Frame
Day 30
Title
Measure of density of blood vessels (number/cm²)
Description
Values measured by immunohistochemistry
Time Frame
Day 30
Title
Measure of normalized fibrosis area (%)
Description
Values measured by immunohistochemistry
Time Frame
Day 30
Title
Measure of reticular basement membrane to bronchial smooth muscle distance (µm)
Description
Values measured by immunohistochemistry
Time Frame
Day 30

10. Eligibility

Sex
All
Minimum Age & Unit of Time
6 Years
Maximum Age & Unit of Time
17 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Child from 6 to 17 years old Having informed consent signed by the holders of parental authority. Having a diagnosis of severe asthma according to the Global Initiative for Asthma (GINA) 2020; Asthma: chronic inflammatory disease of the airways, defined mainly by respiratory symptoms such as wheezing, dyspnea, chest tightness and / or cough, which may vary in time and intensity associated with a limitation also varying in the time of expiratory flow. Severe asthma: asthma which requires treatment with inhaled corticosteroids in high doses plus a second long-acting bronchodilator type controller, to maintain control of symptoms and / or whose control worsens if this treatment is reduced and / or which remains uncontrolled despite this treatment. Having to carry out as part of the current care a functional respiratory exploration; Should require as part of the routine care of a bronchial fibroscopy. Exclusion Criteria: Patient without affiliation or not benefiting from a social security scheme; Patient being in a period of relative exclusion from another protocol; Patient born before 36 weeks of amenorrhea; Patient with a documented history of pulmonary fibrosis, primary pulmonary arterial hypertension, cystic fibrosis, pulmonary malformation or chronic viral infections (hepatitis, HIV); Patient presenting with an exacerbation of asthma requiring systemic corticosteroids within the previous 4 weeks; Patient with any dental, nasopharyngeal or bronchial infection with fever (> 39 ° C) requiring systemic antibiotics within the previous 4 weeks Patient with a contraindication to MRI: Abdominal perimeter greater than 200 cm; Claustrophobia or inability to lie still for 12 minutes; Have a pacemaker or implantable defibrillator, intraocular metallic foreign body, intracranial metal clip, a pre-6000 Starr-Edwards type heart valve prosthesis, or a biomedical device such as an insulin pump or neurostimulator, cochlear implant and metal patch. Patient with a contraindication to anesthesia; Patient with a contraindication to bronchial fibroscopy following: Abnormal hemostasis assessment; Subject with cardiac pathology.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Fabien BEAUFILS, MD
Phone
+335 56 79 55 86
Email
fabien.beaufils@chu-bordeaux.fr
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Fabien BEAUFILS, MD
Organizational Affiliation
University Hospital, Bordeaux
Official's Role
Principal Investigator
Facility Information:
Facility Name
CHU de Bordeaux - Explorations Fonctionnelles
City
Bordeaux
ZIP/Postal Code
33000
Country
France
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Fabien BEAUFILS, MD
Phone
+335 56 79 55 86
Email
fabien.beaufils@chu-bordeaux.fr
First Name & Middle Initial & Last Name & Degree
Mickael FAYON, MD,PhD
First Name & Middle Initial & Last Name & Degree
Patrick BERGER, MD,PhD
First Name & Middle Initial & Last Name & Degree
Fabien BEAUFILS, MD
Facility Name
Centre Hospitalier de Saintonge
City
Saintes
ZIP/Postal Code
17100
Country
France
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Céline NOBILI-DUBARRY, MD
Phone
+335 46 95 15 07
Email
c.nobili-dubarry@ch-saintonge.fr
First Name & Middle Initial & Last Name & Degree
Céline NOBILI-DUBARRY, MD

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
21037369
Citation
Bara I, Ozier A, Tunon de Lara JM, Marthan R, Berger P. Pathophysiology of bronchial smooth muscle remodelling in asthma. Eur Respir J. 2010 Nov;36(5):1174-84. doi: 10.1183/09031936.00019810.
Results Reference
result
PubMed Identifier
21334378
Citation
Girodet PO, Ozier A, Bara I, Tunon de Lara JM, Marthan R, Berger P. Airway remodeling in asthma: new mechanisms and potential for pharmacological intervention. Pharmacol Ther. 2011 Jun;130(3):325-37. doi: 10.1016/j.pharmthera.2011.02.001. Epub 2011 Feb 17.
Results Reference
result
PubMed Identifier
22385633
Citation
Bossley CJ, Fleming L, Gupta A, Regamey N, Frith J, Oates T, Tsartsali L, Lloyd CM, Bush A, Saglani S. Pediatric severe asthma is characterized by eosinophilia and remodeling without T(H)2 cytokines. J Allergy Clin Immunol. 2012 Apr;129(4):974-82.e13. doi: 10.1016/j.jaci.2012.01.059. Epub 2012 Mar 3.
Results Reference
result
PubMed Identifier
34049945
Citation
Benlala I, Dournes G, Girodet PO, Benkert T, Laurent F, Berger P. Evaluation of bronchial wall thickness in asthma using magnetic resonance imaging. Eur Respir J. 2021 Dec 31;59(1):2100329. doi: 10.1183/13993003.00329-2021. Print 2022 Jan. No abstract available.
Results Reference
result
PubMed Identifier
30203889
Citation
Dournes G, Yazbek J, Benhassen W, Benlala I, Blanchard E, Truchetet ME, Macey J, Berger P, Laurent F. 3D ultrashort echo time MRI of the lung using stack-of-spirals and spherical k-Space coverages: Evaluation in healthy volunteers and parenchymal diseases. J Magn Reson Imaging. 2018 Dec;48(6):1489-1497. doi: 10.1002/jmri.26212. Epub 2018 Sep 11.
Results Reference
result

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Analysis of Bronchial Remodeling Using Resonance Magnetic Imaging in Severe Asthmatic childrEn

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