Molecular imaging of calcific aortic valve disease

被引:9
作者
Jung, Jae-Joon [1 ,2 ,4 ]
Jadbabaie, Farid [1 ,2 ,3 ]
Sadeghi, Mehran M. [1 ,2 ,3 ,4 ]
机构
[1] Yale Sch Med, Sect Cardiovasc Med, Cardiovasc Mol Imaging Lab, New Haven, CT USA
[2] Yale Sch Med, Yale Cardiovasc Res Ctr, New Haven, CT USA
[3] Vet Affairs Connecticut Healthcare Syst, West Haven, CT USA
[4] Yale Cardiovasc Res Ctr, 300 George St,770G, New Haven, CT 06511 USA
关键词
Aortic stenosis; aortic valve; molecular imaging; matrix metalloproteinases; FDG; sodium fluoride; POSITRON-EMISSION-TOMOGRAPHY; NATURAL-HISTORY; INFLAMMATION; STENOSIS; HEART; FLUORODEOXYGLUCOSE; PROGRESSION; QUANTIFICATION; MULTIMODALITY; ASSOCIATION;
D O I
10.1007/s12350-017-1158-7
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Calcific aortic valve disease (CAVD) can progress to symptomatic aortic stenosis in a subset of patients. The severity of aortic stenosis and the extent of valvular calcification can be evaluated readily by echocardiography, CT, and MRI using well-established imaging protocols. However, these techniques fail to address optimally other important aspects of CAVD, including the propensity for disease progression, risk of complications in asymptomatic patients, and the effect of therapeutic interventions on valvular biology. These gaps may be addressed by molecular imaging targeted at key biological processes such as inflammation, remodeling, and calcification that mediate the development and progression of CAVD. In this review, recent advances in valvular molecular imaging, including F-18-fluorodeoxyglucose (FDG) and F-18-sodium fluoride (NaF) PET, and matrix metalloproteinase-targeted SPECT imaging in the preclinical and clinical settings are presented and discussed.
引用
收藏
页码:1148 / 1155
页数:8
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