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Respir Med ; 106(1): 145-52, 2012 Jan.
Article in English | MEDLINE | ID: mdl-22056553

ABSTRACT

BACKGROUND: We evaluated whether obstructive sleep apnoea (OSA) and continuous positive airway pressure (CPAP) treatment influence left ventricular (LV) remodelling independently of abdominal obesity and metabolic syndrome (MetS). METHODS: Cardiorespiratory examination, 24-h BP monitoring and echocardiogram were performed in overweight/obese patients with increased abdominal adiposity and symptoms suggesting OSA : OSA/MetS (n.50), OSA/noMetS (n.22), noOSA/MetS (n.29), noOSA/noMets (n.16). The evaluation was repeated in 41 patients after ≥18 months of CPAP. RESULTS: Despite similar age, gender, BMI and 24-h BP, the 2 groups with MetS had greater LV remodelling (LV hypertrophy and diastolic dysfunction) than the 2 groups without MetS. From multiple regression analysis independent determinants for LV mass were MetS, 24-h systolic BP and age, for LV diastolic function were LV mass index, MetS and age. After CPAP, the 20 patients with decreased body weight showed diastolic BP decrease, LV hypertrophy regression and diastolic function improvement, whereas, despite similar respiratory improvement, BP and LV parameters were unchanged in the 21 patients with body weight unchanged/increased. CONCLUSION: In patients with increased abdominal adiposity, LV remodelling is not associated to OSA per se; chronic CPAP treatment does not influence LV remodelling whose regression is mainly linked to body weight decrease.


Subject(s)
Continuous Positive Airway Pressure/adverse effects , Metabolic Syndrome/complications , Obesity, Abdominal/complications , Sleep Apnea, Obstructive/complications , Ventricular Remodeling , Cross-Sectional Studies , Echocardiography , Female , Humans , Longitudinal Studies , Male , Metabolic Syndrome/pathology , Metabolic Syndrome/physiopathology , Middle Aged , Obesity, Abdominal/pathology , Obesity, Abdominal/physiopathology , Sleep Apnea, Obstructive/pathology , Sleep Apnea, Obstructive/physiopathology , Ventricular Function, Left
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