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, …)
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
BASIC_SCIENCE
Masking
NONE
Enrollment
69
Blood sample and vascular exploration.
CHU Montpellier and CHU Nimes
Montpellier, France
University Hospital, Paris
Paris, France
Measure of Flow-Mediated Dilatation (FMD)
Measure of FMD by EndoPAT2000©
Time frame: post exercise and after 4 +/- 2 weeks of training
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)
Time frame: after 4 +/- 2 weeks of training
Number of colonies and function of Endothelial-Colony Formaing cells (ECFC) in vitro
Time frame: post exercise and after 4 +/- 2 weeks of training
Number endothelial progenitors
CD34+, CD45+ and KDR + subpopulations by flow cytometry
Time frame: post exercise and after 4 +/- 2 weeks of training
Vascular function parameters
Systolic pressure index (in AU)
Time frame: after 4 +/- 2 weeks of training
Vascular function parameters
Intima-media thickness (in mm)
Time frame: after 4 +/- 2 weeks of training
Vascular function parameters
Pulse-wave velocity (in ms-1)
Time frame: after 4 +/- 2 weeks of training
Pulse-wave velocity (in ms-1)
Time frame: after 4 +/- 2 weeks of training
Markers of systemic inflammation
C-Reactive protein (in ng/ml)
Time frame: after 4 +/- 2 weeks of training
Markers of oxidative stress
Lipid peroxidation (in micromol/L)
Time frame: after 4 +/- 2 weeks of training
Muscle function parameters
Maximum isometric voluntary contraction (in N.m)
Time frame: after 4 +/- 2 weeks of training
Exercise capacity and vascular adaptation parameters
Maximal oxygen uptake (VO2max, in mL/kg/min)
Time frame: after 4 +/- 2 weeks of training
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