Fibroblast growth factor 23 (FGF23) is a key hormone of the mineral metabolism produced in bone and acting on the kidney to lower phosphatemia. FGF23 is subject to inactivating proteolytic cleavage which results in the presence of C-terminal and N-terminal fragments heretofore described as inactive. We recently showed an increase in FGF23Ct in sickle cell patients, its association with left ventricular mass as well as a direct, pro-hypertrophic effect of FGF23Ct on rat cardiomyocytes. Data from the literature suggest that hypoxia (linked or not to anemia) is responsible for an increase in the production and cleavage of FGF23, either via the hypoxia inducible factor (HIF1α) or via the increase in erythropoietin (EPO). We hypothesize that the FGF23Ct / FGF23i ratio is increased in response to chronic tissue hypoxia, in the absence of anemia, in patients with chronic respiratory failure (CRF) either due to a direct response to hypoxia via the stimulation of HIF1α, or indirectly via the increase in the circulating concentration of EPO. This elevation, if proven, could contribute to the increased risk of heart disease seen in some populations of CRF. We propose to test this hypothesis by assaying FGF23Ct and FGF23i in a cohort of adult CRF patients before and after initiation of oxygen therapy. The object of the present study is to study the FGF23Ct / FGF23i ratio in incident patients presenting with a non treated CRF as well as the modifications of this ratio under oxygen therapy and to study the correlations between FGF23 Ct and FGF23 and i) oxygen saturation and PaO2 ii) echocardiographic parameters and iii) EPO concentrations. Three visits are planned: Baseline (before initiation of oxygen therapy), and two visits after initiation of oxygen therapy, at 3 months (M3) and at 12 months (M12). For each visit, anthropometric and clinical data, treatment and biological results will be collected. FGF23 intact , FGF23 C-terminal and Erythropoietin will be measured. A cardiac ultrasound will be performed at baseline and at M12.
Study Type
OBSERVATIONAL
Enrollment
50
Evaluation of circulating C-terminal FGF23 (FGF23Ct) rate, circulating intact FGF23 (FGF23i) rate and Erythropoietin
12 months after patient enrollment
circulating C-terminal FGF23 (FGF23Ct)
ELISA method
Time frame: at inclusion (before oxygen therapy)
circulating intact FGF23 (FGF23i)
ELISA method
Time frame: at inclusion (before oxygen therapy)
circulating FGF23Ct
ELISA method
Time frame: at month 3 and month 12
circulating FGF23i
ELISA method
Time frame: at month 3 and month 12
circulating erythropoietin
ELISA method
Time frame: at inclusion, month 3 and month 12
arterial O2 saturation
assessed using an arterial sampling
Time frame: at inclusion, month 3 (without and with 02 therapy) and month 12 (without and with 02 therapy)
PaO2 (arterial partial oxygen pressure)
assessed using an arterial sampling
Time frame: at inclusion, month 3 (without and with 02 therapy) and month 12 (without and with 02 therapy)
Assessment of systolic function
left ventricular ejection fraction assessed using cardiac ultrasound
Time frame: at inclusion and month 12
left ventricular mass indexed for body surface area
using cardiac ultrasound
Time frame: at inclusion and month 12
Assessment of diastolic function
Recording of mitral filling flow using cardiac ultrasound
Time frame: at inclusion and month 12
Assessment of pulmonary artery pressure
with measure, using cardiac ultrasound, of * The Vmax of the tricuspid insufficiency flow which gives the systolic gradient right heart ventricle/right heart atrium * And the diameter the inferior vena cava
Time frame: at inclusion and month 12
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