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1.
J Hypertens ; 37(6): 1176-1182, 2019 06.
Article in English | MEDLINE | ID: mdl-30624367

ABSTRACT

OBJECTIVE: Increased carotid stiffness and remodelling is reported in patients with moderate and advanced chronic kidney disease (CKD) and is associated with cardiovascular events. Here, we tested the hypothesis that carotid artery alterations start earlier, during mild CKD. METHODS: Within the Paris Prospective Study 3, a large prospective observational survey of nonreferred people aged 50-75 who received an extensive health check-up, there were 294 participants with glomerular filtration rate (GFR) of at least 45 and less than 60 ml/min per 1.73 m (Stage 3A CKD), 840 participants with GFR 60-89 ml/min per 1.73 m with proteinuria (Stage 2 CKD), 4666 participants with GFR 60-89 ml/min per 1.73 m without proteinuria and 3317 individuals with GFR at least 90 ml/min per 1.73 m at study recruitment. Carotid artery measurements were performed using a high-resolution echotracking device. RESULTS: Compared with patients with GFR at least 90 ml/min per 1.73 m, the carotid distensibility and strain progressively decreased (P for trend <0.0001), whereas carotid stiffness progressively increased (P for trend <0.0001) across GFR categories starting at early stage from GFR 60-89 ml/min per 1.73 m without proteinuria. Higher Young's elastic modulus was observed only for Stage 3A CKD, whereas carotid internal diastolic diameter did not differ between groups. CONCLUSION: The large arterial stiffening starts early during CKD, even in participants with a very mild reduction in renal function.


Subject(s)
Carotid Arteries/physiopathology , Kidney/physiopathology , Renal Insufficiency, Chronic/physiopathology , Aged , Carotid Artery, Common/physiopathology , Elastic Modulus , Female , Glomerular Filtration Rate , Humans , Male , Middle Aged , Prospective Studies , Proteinuria/physiopathology
2.
Medicine (Baltimore) ; 95(2): e2472, 2016 Jan.
Article in English | MEDLINE | ID: mdl-26765449

ABSTRACT

The mechanisms that link metabolic syndrome (MetS) to increased cardiovascular risk are incompletely understood. We examined whether MetS is associated with the neural baroreflex pathway (NBP) and whether any such associations are independent of blood pressure values.This study involved the cross-sectional analysis of data on 2835 subjects aged 50 to 75 years from the Paris Prospective Study 3. The prevalence of MetS was defined according to the American Heart Association/National Heart Blood and Lung Institute definition. NBP values were calculated from the fluctuation of the common carotid distension rate and heart rate using fast Fourier transformation and cross-spectral analysis.The prevalence of MetS was 20.1% in men and 10.4% in women. Compared with controls, subjects with MetS (≥3 components), and those at risk for MetS (1-2 components) had lower NBP (-5.3% and -2.3%, respectively) and higher carotid stiffness (+13.5% and +6.8%, respectively). The negative association between MetS components and NBP was confirmed, even after adjustment for age, sex, and carotid stiffness. After stratification for blood pressure (BP) levels, NBP was reduced only in MetS subjects and those at risk with high BP. The NBP was positively associated with carotid stiffness in controls and subjects at risk for MetS. This association was lost in subjects with MetS, regardless of BP levels.Subjects with MetS had reduced NBP values. The role of BP is fundamental in the reduction of NBP. The mechanisms that link carotid stiffness and NBP are inactive in subjects with MetS, independent of BP levels.


Subject(s)
Baroreflex/physiology , Cardiovascular Diseases/epidemiology , Metabolic Syndrome/epidemiology , Metabolic Syndrome/physiopathology , Vascular Stiffness/physiology , Aged , Analysis of Variance , Cardiovascular Diseases/physiopathology , Carotid Arteries , Comorbidity , Cross-Sectional Studies , Female , France , Humans , Hypertension/epidemiology , Hypertension/physiopathology , Linear Models , Male , Middle Aged , Multivariate Analysis , Prospective Studies , Reference Values , Risk Assessment , Signal Transduction , Vascular Resistance/physiology
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