TY - JOUR
T1 - The different association of epicardial fat with coronary plaque in patients with acute coronary syndrome and patients with stable angina pectoris
T2 - Analysis using integrated backscatter intravascular ultrasound
AU - Harada, Kazuhiro
AU - Harada, Ken
AU - Uetani, Tadayuki
AU - Kataoka, Tadashi
AU - Takeshita, Masahiro
AU - Kunimura, Ayako
AU - Takayama, Yohei
AU - Shinoda, Norihiro
AU - Kato, Bunichi
AU - Kato, Masataka
AU - Marui, Nobuyuki
AU - Ishii, Hideki
AU - Matsubara, Tatsuaki
AU - Amano, Tetsuya
AU - Murohara, Toyoaki
N1 - Publisher Copyright:
© 2014 Elsevier Ireland Ltd.
PY - 2014/10/1
Y1 - 2014/10/1
N2 - Objectives: We assessed the hypothesis that the epicardial fat is associated with coronary lipid plaque. Background: Epicardial fat volume (EFV) is increased in patients with acute coronary syndrome (ACS), and lipid-rich plaques have been associated with acute coronary events. Methods: We enrolled 112 individuals who underwent percutaneous coronary intervention (PCI) (66 with ACS; 46 with stable angina pectoris [SAP]) and classified plaque components using integrated backscatter intravascular ultrasound as calcified, fibrous, or lipid. Possible effects of PCI on plaque data were minimized by assessing 10-mm vessel lengths proximal to the culprit lesions. Total plaque volume and percentage volumes of individual plaque components were calculated. EFV and abdominal visceral fat area were measured using 64-slice computed tomography. Results: ACS patients had significantly higher EFV than did SAP patients (118 ± 44 vs.101 ± 41 mL, p = 0.019). In ACS patients, EFV was correlated with total plaque volume and percentage of lipid plaque (r = 0.27 and 0.31, respectively; p < 0.05). Moreover, an independent interaction between EFV and lipid-rich plaque (odds ratio, 1.04; 95% confidence interval, 1.00-1.07) were revealed. In contrast, in SAP patients, EFV was positively correlated with body mass index and abdominal visceral fat area but not with plaque characteristics. Conclusions: EFV was associated with lipid-rich plaque in patients with ACS, whereas no correlation between EFV and coronary plaque profile was apparent in SAP patients. Epicardial fat may have a role in the development of lipid plaque, which contributes to the pathogenesis of ACS.
AB - Objectives: We assessed the hypothesis that the epicardial fat is associated with coronary lipid plaque. Background: Epicardial fat volume (EFV) is increased in patients with acute coronary syndrome (ACS), and lipid-rich plaques have been associated with acute coronary events. Methods: We enrolled 112 individuals who underwent percutaneous coronary intervention (PCI) (66 with ACS; 46 with stable angina pectoris [SAP]) and classified plaque components using integrated backscatter intravascular ultrasound as calcified, fibrous, or lipid. Possible effects of PCI on plaque data were minimized by assessing 10-mm vessel lengths proximal to the culprit lesions. Total plaque volume and percentage volumes of individual plaque components were calculated. EFV and abdominal visceral fat area were measured using 64-slice computed tomography. Results: ACS patients had significantly higher EFV than did SAP patients (118 ± 44 vs.101 ± 41 mL, p = 0.019). In ACS patients, EFV was correlated with total plaque volume and percentage of lipid plaque (r = 0.27 and 0.31, respectively; p < 0.05). Moreover, an independent interaction between EFV and lipid-rich plaque (odds ratio, 1.04; 95% confidence interval, 1.00-1.07) were revealed. In contrast, in SAP patients, EFV was positively correlated with body mass index and abdominal visceral fat area but not with plaque characteristics. Conclusions: EFV was associated with lipid-rich plaque in patients with ACS, whereas no correlation between EFV and coronary plaque profile was apparent in SAP patients. Epicardial fat may have a role in the development of lipid plaque, which contributes to the pathogenesis of ACS.
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U2 - 10.1016/j.atherosclerosis.2014.07.007
DO - 10.1016/j.atherosclerosis.2014.07.007
M3 - Article
C2 - 25117765
AN - SCOPUS:84907081090
SN - 0021-9150
VL - 236
SP - 301
EP - 306
JO - Atherosclerosis
JF - Atherosclerosis
IS - 2
ER -