Introduction: Epicardial adipose tissue (EAT), accumulated around the heart, is considered an index of visceral adiposity and a promising indicator of high cardio-metabolic risk. Evidences showing that EAT is a metabolically active organ and a source of inflammatory adipo-chemocytokines suggest a condition of chronic inflammation in this small cardiac fat depot. However, the potential links between cardiac adiposity and circulating levels of inflammatory adipo-chemokines, as markers of subclinical inflammation, are not completely understood. Our aim is to evaluate whether cardiac adiposity, measured as EAT thickness, is related to Regulated on activation, Normal T Cell Expressed and Secreted (RANTES/CCL5) levels, in obese patients. Methods: EAT thickness (meauserd by echocardiography, on the free wall of right ventricle), RANTES/CCL5 and other inflammatory markers (by ELISA kit) were measured in 36 women with uncomplicated obesity (OB) (BMI 41.6±5.6 kg/m2) and 15 normal-weight controls. Abdominal visceral adipose tissue (VAT) and subcutaneous adipose tissue (SAT) were assessed by computed tomography (CT). Results: OB patients had thicker EAT (6.8±0.9 vs. 1.3±0.3 mm, p<0.0001) (Fig.1) and higher RANTES/CCL5 levels (2468.9±745.5 vs. 1272.1±413.7 pg/ml, p<0.03) than controls (Fig. 2). The EAT thickness positively correlated with RANTES/CCL5 concentrations (r2=0.65, p<0.001) (Fig.3). Moreover, EAT thickness and RANTES/CCL5 concentration were directly correlated with indices of fat distribution (VAT, VAT/SAT and waist, p<0.001 for all). Notably, when using multiple regression analysis, RANTES/CCL5 levels most closely correlated with EAT thickness (t=3.93) and VAT areas (t=3.77), while other indices of fat distribution did not enter the model. Conclusions: EAT thickness, an indicator of cardiac adiposity, may be related to inflammatory adipo-chemokines in visceral-obese patients and might be used as a reliable marker of visceral adiposity. The elevated RANTES/CCL5 levels, contributing to the pro-inflammatory state, may also lead to cardio-metabolic disorders.
Regulated on activation, normal-T cell expressed and secreted (RANTES/CCL5) levels: an association with epicardial visceral fat thickness / E. Vianello, A.E. Malavazos, F. Bandera, M.M. Corsi Romanelli, E. Dozio. ((Intervento presentato al convegno Young scientist meeting SIPMeT tenutosi a Milano nel 2017.
Regulated on activation, normal-T cell expressed and secreted (RANTES/CCL5) levels: an association with epicardial visceral fat thickness
E. Vianello;A.E. Malavazos;F. Bandera;M.M. Corsi Romanelli;E. Dozio
2017
Abstract
Introduction: Epicardial adipose tissue (EAT), accumulated around the heart, is considered an index of visceral adiposity and a promising indicator of high cardio-metabolic risk. Evidences showing that EAT is a metabolically active organ and a source of inflammatory adipo-chemocytokines suggest a condition of chronic inflammation in this small cardiac fat depot. However, the potential links between cardiac adiposity and circulating levels of inflammatory adipo-chemokines, as markers of subclinical inflammation, are not completely understood. Our aim is to evaluate whether cardiac adiposity, measured as EAT thickness, is related to Regulated on activation, Normal T Cell Expressed and Secreted (RANTES/CCL5) levels, in obese patients. Methods: EAT thickness (meauserd by echocardiography, on the free wall of right ventricle), RANTES/CCL5 and other inflammatory markers (by ELISA kit) were measured in 36 women with uncomplicated obesity (OB) (BMI 41.6±5.6 kg/m2) and 15 normal-weight controls. Abdominal visceral adipose tissue (VAT) and subcutaneous adipose tissue (SAT) were assessed by computed tomography (CT). Results: OB patients had thicker EAT (6.8±0.9 vs. 1.3±0.3 mm, p<0.0001) (Fig.1) and higher RANTES/CCL5 levels (2468.9±745.5 vs. 1272.1±413.7 pg/ml, p<0.03) than controls (Fig. 2). The EAT thickness positively correlated with RANTES/CCL5 concentrations (r2=0.65, p<0.001) (Fig.3). Moreover, EAT thickness and RANTES/CCL5 concentration were directly correlated with indices of fat distribution (VAT, VAT/SAT and waist, p<0.001 for all). Notably, when using multiple regression analysis, RANTES/CCL5 levels most closely correlated with EAT thickness (t=3.93) and VAT areas (t=3.77), while other indices of fat distribution did not enter the model. Conclusions: EAT thickness, an indicator of cardiac adiposity, may be related to inflammatory adipo-chemokines in visceral-obese patients and might be used as a reliable marker of visceral adiposity. The elevated RANTES/CCL5 levels, contributing to the pro-inflammatory state, may also lead to cardio-metabolic disorders.File | Dimensione | Formato | |
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