Epicardial adipose tissue is related to arterial stiffness and inflammation in patients with cardiovascular disease and type 2 diabetes

被引:36
作者
Al-Talabany, Shaween [1 ]
Mordi, Ify [1 ]
Houston, J. Graeme [1 ,2 ]
Colhoun, Helen M. [3 ]
Weir-McCall, Jonathan R. [1 ]
Matthew, Shona Z. [1 ]
Looker, Helen C. [4 ]
Levin, Daniel [1 ]
Belch, Jill J. F. [1 ]
Dove, Fiona [1 ]
Khan, Faisel [1 ]
Lang, Chim C. [1 ]
机构
[1] Univ Dundee, Ninewells Hosp & Med Sch, Div Mol & Clin Med, Mailbox 2, Dundee DD1 9SY, Scotland
[2] Ninewells Hosp, NHS Tayside Clin Radiol, Dundee DD1 9SY, Scotland
[3] Univ Edinburgh, Inst Genet & Mol Med, Edinburgh EH4 2XU, Midlothian, Scotland
[4] Univ Dundee, Dundee Epidemiol & Biostat Unit, Dundee DD1 9SY, Scotland
来源
BMC CARDIOVASCULAR DISORDERS | 2018年 / 18卷
基金
英国惠康基金;
关键词
Epicardial adipose tissue; Pulse wave velocity; Arterial stiffness; Cardiovascular magnetic resonance; Left ventricular mass; Type 2 diabetes mellitus; LEFT-VENTRICULAR STRUCTURE; CORONARY-HEART-DISEASE; PERICARDIAL FAT; ATHEROSCLEROTIC BURDEN; OBESITY; VOLUME; ASSOCIATION; ACTIVATION; THICKNESS; CELLS;
D O I
10.1186/s12872-018-0770-z
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Epicardial adipose tissue (EAT) is an emerging cardio-metabolic risk factor and has been shown to correlate with adverse cardiovascular (CV) outcome; however the underlying pathophysiology of this link is not well understood. The aim of this study was to evaluate the relationship between EAT and a comprehensive panel of cardiovascular risk biomarkers and pulse wave velocity (PWV) and indexed left ventricular mass (LVMI) in a cohort of patients with cardiovascular disease (CVD) and diabetes compared to controls. Methods: One hundred forty-five participants (mean age 63.9 +/- 8.1 years; 61% male) were evaluated. All patients underwent cardiovascular magnetic resonance (CMR) examination and PWV. EAT measurements from CMR were performed on the 4-chamber view. Blood samples were taken and a range of CV biomarkers was evaluated. Results: EAT measurements were significantly higher in the groups with CVD, with or without T2DM compared to patients without CVD or T2DM (group 1 EAT 15.9 +/- 5.5 cm(2) vs. group 4 EAT 11.8 +/- 4.1 cm(2), p = 0.001; group 3 EAT 15.1 +/- 4.3 cm(2) vs. group 4 EAT 11.8 +/- 4.1 cm(2), p = 0.024). EAT was independently associated with IL-6 (beta 0. 2, p = 0.019). When added to clinical variables, both EAT (beta 0.16, p = 0.035) and IL-6 (beta 0.26, p = 0.003) were independently associated with PWV. EAT was significantly associated with LVMI in a univariable analysis but not when added to significant clinical variables. Conclusions: In patients with cardio-metabolic disease, EAT was independently associated with PWV. EAT may be associated with CVD risk due to an increase in systemic vascular inflammation. Whether targeting EAT may reduce inflammation and/or cardiovascular risk should be evaluated in prospective studies.
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页数:8
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