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Visceral obesity,but not central obesity,is associated with cardiac remodeling in subjects with suspected metabolic syndrome
Authors:D.-H. Cho  M.-N. Kim  H.J. Joo  W.J. Shim  D.-S. Lim  S.-M. Park
Affiliation:Korea University Anam Hospital, Seoul, Republic of Korea
Abstract:

Background and aims

Metabolic syndrome (MetS) is a cluster of multiple risk factors including central obesity that may lead to cardiac damage and cardiovascular events. We investigated whether visceral obesity induces cardiac structural and functional remodeling independently from central obesity and other risk factors in subjects with suspected MetS.

Methods and results

We studied 229 participants with suspected MetS. Visceral fat area (VFA) was measured by bioelectrical impedance analysis. Left ventricular (LV) mass index, early diastolic velocity of mitral annulus (e′), and LV global longitudinal strain (GLS) were measured by echocardiography. Subjects were categorized into high and low VFA group (VFAh and VFAl). MetS was more prevalent in the VFAh than in the VFAl (p = 0.004). The VFAh had a higher waist circumference (WC) than the VFAl (p < 0.001). LV mass index was higher, but e' and GLS were lower in the VFAh than in VFAl (all p < 0.05). VFA was well correlated with blood pressure, fasting blood glucose, triglyceride, high-sensitivity C-reactive protein and adiponectin (all p < 0.05). VFA was correlated to LV mass index, e’, and GLS (all p < 0.05) and was independently associated with GLS after adjustment for other risk factors, including WC (p = 0.005).

Conclusions

Visceral obesity assessed by VFA was well correlated with parameters of MetS. Visceral obesity, but not central obesity measured by WC, was independently associated with structural and functional cardiac remodeling in subjects with suspected MetS. It suggests that visceral obesity should be considered as an important risk factor for cardiac damage in dysmetabolic subjects.

Trial registration

NCT02077530 (date of registration: November 1, 2013).
Keywords:Visceral obesity  Visceral fat  Cardiovascular disease  Metabolic syndrome  MetS  metabolic syndrome  2D  two-dimensional  LV  left ventricular  GLS  global longitudinal strain  VFA  visceral fat area  BMI  body mass index  WC  waist circumference  SBP  systolic blood pressure  DBP  diastolic blood pressure  HDL  high-density lipoprotein  TG  triglycerides  hs-CRP  high-sensitivity C-reactive protein  the low and high VFA group  early diastolic velocity of mitral annulus
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