Acute kidney injury (AKI) is a frequent disease in conventional hospital departments and in intensive care units. It's associated with a high risk to develop chronic kidney disease (CKD), even after a single small AKI episode. It's also associated with an important morbi-mortality, particularly cardiovascular (CV). Some studies have already showed a link between AKI and CV risk but pathologic mechanisms implicated are still unknown. In AKI and CKD, numerous substances, called uremic toxins (UT) are accumulating in blood. In CKD, those toxins, and particularly Indoxyl sulfate (IS), are known to have cardiac and vascular deleterious consequences. However, in AKI, whether acute accumulation of UT may trigger CV complications is unknown. The purpose of this study is that during AKI, a high UT concentration, in particular IS, would be associated with early vascular and cardiac dysfunctions that can be characterized by the persistence of an accelerated pulse wave velocity (PWV). The main objective is to evaluate the correlation between UT concentrations (especially IS) and arterial stiffness (PWV measurement) at three months of an AKI episode in conventional hospital departments and in the intensive care unit of nephrology.
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
OTHER
Masking
DOUBLE
Enrollment
105
Blood sample withdrawal will be done and serum creatinine, IS, PCS, FGF-23, Angiopoietin-2, VCAM-1, E-Selectin and Troponin will be measured.
Amiens hospital
Amiens, France
RECRUITINGChange of pulse wave velocity (PWV) measurement from baseline
Time frame: at 3 months
Correlation between Para-cresyl Sulfate (PCS) concentration and PWV
Time frame: 3 months
Correlation between Fibroblast Growth Factor 23 (FGF23) concentration and PWV
Time frame: 3 months
Correlation between Fibroblast Growth Factor 23 (FGF23) concentration and arterial pressure measurement
Time frame: 3 months
Correlation between Fibroblast Growth Factor 23 (FGF23) concentration and cardiac diastolic function
Time frame: 3 months
Correlation between IS concentration and arterial pressure measurement
Time frame: 3 months
Correlation between IS concentration and cardiac diastolic function
Time frame: 3 months
Correlation between Para-cresyl Sulfate (PCS) concentration and arterial pressure measurement
Time frame: 3 months
Correlation between Para-cresyl Sulfate (PCS) concentration and cardiac diastolic function
Time frame: 3 months
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