Quantification and 3D reconstruction of atherosclerotic plaque components in apolipoprotein E knockout mice using ex vivo high-resolution MRI

被引:32
作者
McAteer, MA
Schneider, JE
Clarke, K
Neubauer, S
Channon, KM
Choudhury, RP
机构
[1] Univ Oxford, Dept Cardiovasc Med, Oxford OX1 2JD, England
[2] Univ Oxford, Univ Lab Physiol, Oxford OX1 2JD, England
关键词
atherosclerosis; brachiocephalic artery; apoE; -/-; mice; MRI; lipid-rich/necrotic core;
D O I
10.1161/01.ATV.0000146811.19029.fb
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective - To investigate the ability of high-resolution MRI to determine composition and microanatomy of atherosclerosis in mouse aortic root and brachiocephalic artery. Methods and Results - Aortic root and brachiocephalic arteries of apolipoprotein E knockout (apoE-/-) mice fed Western diet for 10, 20, or 30 weeks were imaged ex vivo (11.7 T; 3D multiecho sequence; resolution 47 x 47 x 62.5 mum). Using semiautomated histogram-based methods, MRI accurately quantified lipid-rich/necrotic areas in the aortic root (r(2) = 0.84; P < 0.001) and brachiocephalic artery (r(2) = 0.90; P < 0.001) compared with histology. Similarly, cell-rich caps in aortic roots, quantified by MRI and histology, correlated closely (r(2) = 0.74; P < 0.001). Reconstruction of segmented brachiocephalic arteries in 3D provided unique insights into plaque microanatomy and enabled volumetric quantification of plaque and lipid-rich/necrotic core. Between 10 and 30 weeks, 3D measurement identified an 11.6-fold increase in plaque volume (versus 4.1-fold for 2D) and a 21.3-fold increase in plaque lipid-rich/necrotic core volume (versus 6.4-fold for 2D), indicating superior power of 3D quantification. Conclusions - Ex-vivo high-resolution 3D MRI accurately quantified lipid-rich/ necrotic core and cell-rich cap areas in atherosclerotic lesions in apoE-/- mice. Reconstruction and volumetric quantification of segmented brachiocephalic arteries demonstrated greater sensitivity in detecting changes in plaque size and lipid composition over time than 2D analysis.
引用
收藏
页码:2384 / 2390
页数:7
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