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The hypothesis is that pulmonary and cardiac proton MRI allows phenotyping of patients with bronchial obstruction by cluster analysis based on quantitative multimodal imaging of bronchi, pulmonary vessels, pulmonary parenchyma, right and left ventricular function, myocardial fibrosis and pulmonary arterial pressure.
Such imaging will also offer the advantage of being non-irradiating and without contrast products, which will ultimately allow CT to be replaced by MRI in the follow-up of bronchial obstructive patients, thus avoiding the risks associated with repeated exposure to ionizing radiation.
Bronchial obstructive diseases such as asthma and chronic obstructive pulmonary disease (COPD) are very common and represent a major public health problem. The distinction between these two diseases is sometimes difficult. In each of these diseases, several clinical phenotypes or biological endotypes have been defined. For example, frequent exacerbating patients and / or hypereosinophilic patients are present in both diseases. In the severe states, cardiovascular comorbidities are the most frequent comorbidities and alter the prognosis.
In these chronic obstructive patients, computed tomography (CT) allows a multimodal analysis of the bronchial wall, the lung parenchyma and pulmonary vessels. CT also allows a score analysis of coronary plaques. However, irradiation is significant and increases with repeated examinations. CT does not allow a comprehensive analysis of cardiac function, or an estimate of pulmonary artery pressure.
Magnetic Resonance Imaging (MRI) is a proton non-ionizing alternative to CT, in particular when using 3D ultra-short echo-time (UTE) sequences. These 3D-UTE sequences decrease the effects of magnetic susceptibility and provide morphological and morphometric information on bronchi and lung comparable to those obtained by CT. Moreover, dedicated sequences add functional information on bronchi. Heart MRI allows more analyses, such as right and left ventricular systolic functions, an indirect estimate of pulmonary arterial pressure and the amount of diffuse myocardial fibrosis.
Our project aims to identify morphological phenotypes through the pulmonary and heart MRI in patients with obstructive lung disease
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| COPD | Other | COPD according to GOLD 2019 but unrestricted to any level of bronchial reversibility established by the pulmonologist |
|
| Asthma | Other | asthma according to GINA 2019 but without any smoking restriction |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| MRI | Procedure | The procedure to study lung and heart MRI, performed on a 1.5T magnet (Siemens), without any injection or inhalation of contrast agent |
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| Measure | Description | Time Frame |
|---|---|---|
| Determine the number of the clusters | Number of the clusters will be defined using principal component analysis and dendrogram, based on the multimodal lung and heart MRI analysis | Day 30 |
| Determine the Quality of the clusters | Quality of the clusters will be defined using Dunn index and non-hierarchical analysis based on the multimodal lung and heart MRI analysis | Day 30 |
| Measure | Description | Time Frame |
|---|---|---|
| Assessment of age | Day 1 | |
| Assessment of sexe | Day 1 | |
| Assessment of tobacco consumption |
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Affiliation | Role |
|---|---|---|
| Patrick BERGER, MD, PhD | University Hospital, Bordeaux | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Centre hospitalier de la Côte Basque | Bayonne | 64100 | France | |||
| Clinique Saint Augustin |
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diagnostic imaging pilot study, exploratory, prospective, multi-center
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| Day 1 |
| Assessment of disease duration | Day 1 |
| Evaluation score of SF-36 questionnaire | Determine the quality of life. SF36: 36-Item Short Form health survey Minimum = 0 and maximum = 100 Higher score means better outcome | Day 1 |
| Evaluation with St Georges Quality of Life Questionnaire | Determine the quality of life. Minimum = 0 and maximum = 100 Higher score means worse outcome | Day 30 |
| Evaluation of comorbidities | The presence of various comorbidities will be checked in a yes/No manner :
| Day 1 |
| Determine of Forced Expiratory Volume in one sec (FEV-1) during spirometry before and after bronchodilator | Assessment of FEV-1/FVC during spirometry before and after bronchodilator | day 1 |
| Determine of Forced Vital Capacity (FVC) during spirometry before and after bronchodilator | Assessment of FEV-1/FVC during spirometry before and after bronchodilator | day 1 |
| Determine of slow Vital Capacity (VC) during spirometry before and after bronchodilator | day 1 |
| Determine of Total Lung Capacity (TLC) during spirometry before and after bronchodilator | day 1 |
| Determine of Functional Residual Capacity (FRC) during spirometry before and after bronchodilator | day 1 |
| Determine of Residual Volume (RV) during spirometry before and after bronchodilator | day 1 |
| Determine of Carbon monoxide transfer capacity (TLCO) | day 1 |
| Determine the value of blood heamoglobin | day 1 |
| Determine the value of blood eosinophils | day 1 |
| Determine the value of blood C-reactive protein | day 1 |
| Determine the value of blood B-type natriuretic peptide | day 1 |
| Determine the value of blood total IgE at | day 1 |
| Determine the value of blood total IgE | day 1 |
| Bordeaux |
| 33000 |
| France |
| Centre Médical Toki Eder | Cambo-les-Bains | 64250 | France |
| Hôpital Le Cluzeau - CHU de Limoges | Limoges | 87000 | France |
| Centre de Pneumologie Bordeaux Rive droite | Lormont | 33310 | France |
| Hôpital Haut-Lévêque - CHU de Bordeaux | Pessac | 33600 | France |