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| ID | Type | Description | Link |
|---|---|---|---|
| 2018-A02886-49 | Registry Identifier | ID-RCB |
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Analyses will be carried out with the recruited population.
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| Name | Class |
|---|---|
| University Hospital, Paris | OTHER |
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Vascular comorbidities constitute a major burden in COPD patients. The atherosclerosis process is preceded by the onset of an endothelial dysfunction (assessed by the flow-mediated dilatation (FMD)), which is a risk factor for later ischemic vascular complications and death. In COPD, this endothelial dysfunction could be explained by intrinsic endothelial cell properties, or the effect of a pathogenic endothelial cell microenvironment (inflammation and/or oxidative stress). Exercise training constitue a powerful stimulus for the endothelial function, and could be mediated by the mobiliaztion and function of endothelial progenitors. While exercise training is an efficient intervention in COPD patients, its vascular effect appear blunted. The endothelial function response to training has appeared heterogeneous in COPD patients, and possibly linked to the endothelial cel lesion. Thus, endothelial function (assessed by the FMD) response to exercise training would be lower in COPD patients with a baseline impairment of the their FMD. In addition, of biological and functional factors could explained the magnitude of the FMD response in COPD patients.The aim of the study are thus :
To compare the FMD change in COPD patients with FMD above (FMD+) and under the median FMD (FMD-) after 4 weeks of exercise training in the whole study population.
To compare between COPD patients FMD+, COPD patients FMD- and healthy "control" subjects, the endothelial inflammation and senescence at baseline and the endothelial progenitor mobilization and function change induced by exercise (maximal exercise test and training).
To compare between COPD patients FMD+, COPD patients FMD- and healthy "control" subjects the effect of the endothelial microenvironment on the cellular pathways regulating the endothelial function in vitro at baseline and changes after exercise training.
To test in COPD patients the association between the magnitude of the FMD changes after training and biological, functional and clinical factors (inflammation oxidative stress markers, endothelial biomarkers, pulmonary impairment and phenotype, cardiovascular risks factors, vascular function, metabolic markers, physical activity level, …)
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| COPD patients | Experimental | FMD analysis Endothelial progenitors Exercise test Exercise training |
|
| Healthy subject | Experimental | FMD analysis Endothelial progenitors Exercise test |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| FMD analysis | Other | Blood sample and vascular exploration. |
|
| Measure | Description | Time Frame |
|---|---|---|
| Measure of Flow-Mediated Dilatation (FMD) | Measure of FMD by EndoPAT2000© | post exercise and after 4 +/- 2 weeks of training |
| Measure | Description | Time Frame |
|---|---|---|
| Measure of biological vascular markers | E-selectin soluble (sE-sel), endotheline 1 (ET1), facteur von Willebrand (vWF), vascular endothelial growth factor A (VEGF-A), Fms-like tyrosine kinase receptor 1 soluble (sFlt-1), Angiopoietine 1 et 2 (Ang-1 Ang-2) | after 4 +/- 2 weeks of training |
| Number of colonies and function of Endothelial-Colony Formaing cells (ECFC) in vitro |
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Inclusion Criteria:
A/ COPD patients
B/ Healthy subjects
Exclusion Criteria:
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| Name | Affiliation | Role |
|---|---|---|
| Fares Gouzi, MD, PhD | UH Montpellier | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| CHU Montpellier and CHU Nimes | Montpellier | 34295 | France | |||
| University Hospital, Paris |
| PubMed Identifier | Type | Citation | Retractions |
|---|---|---|---|
| 36372120 | Result | Gouzi F, Dubois-Gamez AS, Lacoude P, Abdellaoui A, Hedon C, Charriot J, Boissin C, Vachier I, Hayot M, Molinari N, Bourdin A. Feasibility of a nasal breathing training during pulmonary rehabilitation. A pilot randomized controlled study. Respir Physiol Neurobiol. 2023 Feb;308:103987. doi: 10.1016/j.resp.2022.103987. Epub 2022 Nov 11. |
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| ID | Term |
|---|---|
| D029424 | Pulmonary Disease, Chronic Obstructive |
| ID | Term |
|---|---|
| D008173 | Lung Diseases, Obstructive |
| D008171 | Lung Diseases |
| D012140 | Respiratory Tract Diseases |
| D002908 | Chronic Disease |
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COPD patient group (n=50) and Healthy control Group (n=24)
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| post exercise and after 4 +/- 2 weeks of training |
| Number endothelial progenitors | CD34+, CD45+ and KDR + subpopulations by flow cytometry | post exercise and after 4 +/- 2 weeks of training |
| Vascular function parameters | Systolic pressure index (in AU) | after 4 +/- 2 weeks of training |
| Vascular function parameters | Intima-media thickness (in mm) | after 4 +/- 2 weeks of training |
| Vascular function parameters | Pulse-wave velocity (in ms-1) | after 4 +/- 2 weeks of training |
| Pulse-wave velocity (in ms-1) | after 4 +/- 2 weeks of training |
| Markers of systemic inflammation | C-Reactive protein (in ng/ml) | after 4 +/- 2 weeks of training |
| Markers of oxidative stress | Lipid peroxidation (in micromol/L) | after 4 +/- 2 weeks of training |
| Muscle function parameters | Maximum isometric voluntary contraction (in N.m) | after 4 +/- 2 weeks of training |
| Exercise capacity and vascular adaptation parameters | Maximal oxygen uptake (VO2max, in mL/kg/min) | after 4 +/- 2 weeks of training |
| Paris |
| 75015 |
| France |
| D020969 |
| Disease Attributes |
| D010335 | Pathologic Processes |
| D013568 | Pathological Conditions, Signs and Symptoms |