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Pro-atherogenic mediators and subclinical atherogenesis are related to epicardial adipose tissue thickness in patients with cardiovascular risk

Authors :
Paul Mondragón-Terán
Alberto Melchor-López
Sofía L Alcaráz-Estrada
Lilia Amezcua
Juan Antonio Suárez-Cuenca
Carlos Haroldo Ixcamparij-Rosales
Juan Ángel Peraza-Zaldivar
Nuria Guerrero-Celis
Rocío Aceves-Millán
Rebeca Pérez-Cabeza de Vaca
Source :
The Journal of International Medical Research
Publication Year :
2016
Publisher :
SAGE Publications, 2016.

Abstract

ObjectiveTo evaluate the relationship between pro-atherogenic biomarkers and epicardial adipose tissue (EAT) thickness in patients with cardiovascular risk factors.MethodsPlasma nitric oxide (NO), soluble intercellular adhesion molecule-1 and malondialdehyde (MDA) levels, EAT thickness, flow-mediated dilation (FMD) and carotid intima media thickness (CIMT) were determined in patients aged >18 years who were referred for echocardiography for heart ischemia or non-ischemic diseases. Cardiovascular risk factors (Framingham score [FS] ≥ 20) were weighted.ResultsHypertension, dyslipidaemia and type 2 diabetes mellitus were prevalent (≥55% of 40 patients). Patients with FS ≥ 20 ( n = 21) showed significantly higher EAT and CIMT values. Globally, MDA, CIMT, age, waist circumference, high-density lipoprotein cholesterol (HDL-C) and FS were associated with EAT thickness. EAT was significantly associated with NO in patients with FS ≥ 20. Significant differences in EAT thickness were found between patients stratified by NO value, FMD, age, smoking status, dyslipidaemia, type 2 diabetes mellitus and FS. An EAT-associated atherogenic risk (CIMT ≥ 1 mm) model was statistically significant when MDA and type 2 diabetes mellitus were included.ConclusionEAT thickness was associated with MDA, CIMT, age, waist circumference, HDL-C and FS globally, but with NO only in patients with FS≥20. EAT may be used to identify vascular damage stage, possibly influenced by MDA and type 2 diabetes mellitus.

Details

ISSN :
14732300 and 03000605
Volume :
45
Database :
OpenAIRE
Journal :
Journal of International Medical Research
Accession number :
edsair.doi.dedup.....73acbf6b47af6b5628140061a744017d
Full Text :
https://doi.org/10.1177/0300060516655245