Vulnerable plaque detection by 3.0 tesla magnetic resonance imaging

被引:35
作者
Cury, RC
Houser, SL
Furie, KL
Stone, JR
Ogilvy, CS
Sherwood, JB
Muller, JE
Brady, TJ
Hinton, DP
机构
[1] Massachusetts Gen Hosp, Dept Radiol, Athinoula A Martinos Ctr Biomed Imaging, Charlestown, MA 02129 USA
[2] Massachusetts Gen Hosp, Dept Pathol, Charlestown, MA 02129 USA
[3] Massachusetts Gen Hosp, Div Neurol, Charlestown, MA 02129 USA
[4] Massachusetts Gen Hosp, Div Neurosurg, Charlestown, MA 02129 USA
[5] Massachusetts Gen Hosp, Div Cardiol, Charlestown, MA 02129 USA
关键词
3.0 tesla MRI; vulnerable plaque; carotid artery; vessel wall imaging;
D O I
10.1097/01.rli.0000186419.55504.30
中图分类号
R8 [特种医学]; R445 [影像诊断学];
学科分类号
1002 ; 100207 ; 1009 ;
摘要
Rationale and Objectives: A clinical case report is presented on a 76-year-old man who volunteered for a 3.0 T magnetic resonance (MR) carotid protocol. The subject was referred for carotid endarterectomy and histology was performed on the ex vivo specimen an compared with the in vivo images. Methods: The 3.0 and 1.5 T (obtained for comparison) MR protocol consisted of 2-dimensional (2D) and 3-dimensional (3D) multicontrast bright and black blood imaging for detecting the lumen an vessel wall. Results: The combination of multicontrast black blood transverse images and the 3D time of flight transverse images provided visualization of a narrowed internal carotid artery lumen 4 mm above of the bifurcation and the presence of a complex atherosclerotic plaque containing a large lipid pool, calcification, and intact fibrous cap. Quantitative comparisons including vessel lumen and plaque area, signal-to-noise (SNR) and contrast-to-noise (CNR) ratios were obtained for 1.5 and 3.0 T image data. Plaque composition was verified with histology. Macrophages were also detected in the shoulders of the plaque as demonstrated by CD68 staining and corresponded with a small hyperintense area in the T2W images at 3.0 T, but not observed in comparable 1.5 T images. Conclusions: High field 3.0 T multicontrast MRI of atherosclerotic plaque has been validated with histology comparison and provides improved detection of complex atherosclerotic plaque with increased SNR and CNR compared with 1.5 T. Further studies validating contrast mechanisms of plaque at 3.0 T are required, but atherosclerotic plaque imaging has clear benefit from application at the higher magnetic field strength.
引用
收藏
页码:112 / 115
页数:4
相关论文
共 10 条
[1]   Spontaneous acute dissection of the internal carotid artery -: High-resolution magnetic resonance imaging at 3.0 tesla with a dedicated surface coil [J].
Bachmann, R ;
Nassenstein, I ;
Kooijman, H ;
Dittrich, R ;
Kugel, H ;
Niederstadt, T ;
Kuhlenbäumer, G ;
Ringelstein, EB ;
Krämer, S ;
Heindel, W .
INVESTIGATIVE RADIOLOGY, 2006, 41 (02) :105-111
[2]   Initial experiences with in vivo right coronary artery human MR vessel wall imaging at 3 tesla [J].
Botnar, RM ;
Stuber, M ;
Lamerichs, R ;
Smink, J ;
Fischer, SE ;
Harvey, P ;
Manning, WJ .
JOURNAL OF CARDIOVASCULAR MAGNETIC RESONANCE, 2003, 5 (04) :589-594
[3]   Contrast enhancement in atherosclerosis development in a mouse model:: in vivo results at 2Tesla [J].
Chaabane, L ;
Pellet, N ;
Bourdillon, MC ;
Mansard, CD ;
Sulaiman, A ;
Hadour, G ;
Thivolet-Béjui, F ;
Roy, P ;
Briguet, A ;
Douek, P ;
Soulas, EC .
MAGNETIC RESONANCE MATERIALS IN PHYSICS BIOLOGY AND MEDICINE, 2004, 17 (3-6) :188-195
[4]   High-resolution magnetic resonance imaging at 2 Tesla: Potential for atherosclerotic lesions exploration in the apolipoprotein E knockout mouse [J].
Chaabane, L ;
Soulas, EC ;
Contard, F ;
Salah, A ;
Guerrier, D ;
Briguet, A ;
Douek, P .
INVESTIGATIVE RADIOLOGY, 2003, 38 (08) :532-538
[5]   Atherosclerotic lesions in genetically modified mice quantified in vivo by non-invasive high-resolution magnetic resonance microscopy [J].
Choudhury, RP ;
Aguinaldo, JG ;
Rong, JX ;
Kulak, JL ;
Kulak, AR ;
Reis, ED ;
Fallon, JT ;
Fuster, V ;
Fisher, EA ;
Fayad, ZA .
ATHEROSCLEROSIS, 2002, 162 (02) :315-321
[6]   Noninvasive in vivo high-resolution magnetic resonance imaging of atherosclerotic lesions in genetically engineered mice [J].
Fayad, ZA ;
Fallon, JT ;
Shinnar, M ;
Wehrli, S ;
Dansky, HM ;
Poon, M ;
Badimon, JJ ;
Charlton, SA ;
Fisher, EA ;
Breslow, JL ;
Fuster, V .
CIRCULATION, 1998, 98 (15) :1541-1547
[7]   Noncoronary and coronary atherothrombotic plaque imaging and monitoring of therapy by MRI [J].
Fayad, ZA .
NEUROIMAGING CLINICS OF NORTH AMERICA, 2002, 12 (03) :461-+
[8]  
HINTON DP, 2003, 11 ANN ISMRM TOR CAN
[9]  
Rutt Brian K., 2004, Current Drug Targets - Cardiovascular & Haematological Disorders, V4, P147, DOI 10.2174/1568006043336393
[10]   MRI of atherosclerosis [J].
Yuan, C ;
Kerwin, WS .
JOURNAL OF MAGNETIC RESONANCE IMAGING, 2004, 19 (06) :710-719