Cardiac PET perfusion tracers: current status and future directions.
Cardiac PET perfusion tracers: current status and future directions.
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DOI:
10.1053/j.semnuclmed.2014.06.011
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发表时间:
2014-09
影响因子:
4.9
通讯作者:
Packard RR
中科院分区:
文献类型:
--
作者:
Maddahi J;Packard RR
Positron emission tomography (PET) myocardial perfusion imaging (MPI) is increasingly used for non-invasive detection and evaluation of coronary artery disease (CAD). However, the widespread use of PET MPI has been limited by shortcomings of the current PET perfusion tracers. Availability of these tracers is limited by need for an on-site (15O water and 13N ammonia) or nearby (13N ammonia) cyclotron or commitment to costly generators (82Rb). Due to short half-lives ranging from 76sec for 82Rb, to 2.1min for 15O water and 10min for 13N ammonia, their use in conjunction with treadmill exercise stress testing is either not possible (82Rb and 15O water) or is not practical (13N ammonia). Furthermore, the long positron range of 82Rb makes image resolution suboptimal and its low extraction limits its defect resolution. In recent years, development of an 18F labeled PET perfusion tracer has gathered considerable interest. The longer half-life of 18F (108 minutes) would make the tracer available as a unit dose from regional cyclotrons and allow use in conjunction with treadmill exercise testing. Furthermore, the short positron range of 18F would result in better image resolution. 18F flurpiridaz is by far the most thoroughly studied in animal models, and is the only F18-based PET MPI radiotracer currently undergoing clinical evaluation. Pre-clinical and clinical experience with 18F flurpiridaz demonstrated a high myocardial extraction fraction, high image and defect resolution, high myocardial uptake, slow myocardial clearance, and high myocardial-to-background contrast which was stable over time – important properties of an ideal PET MPI radiotracer. Pre-clinical data from other 18F labeled myocardial perfusion tracers are encouraging.
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DOI:
10.2967/jnumed.104.007831
发表时间:
2009-07
期刊:
Journal of nuclear medicine : official publication, Society of Nuclear Medicine
影响因子:
--
作者:
El Fakhri G;Kardan A;Sitek A;Dorbala S;Abi-Hatem N;Lahoud Y;Fischman A;Coughlan M;Yasuda T;Di Carli MF
通讯作者:
Di Carli MF
影响因子:
37.8
作者:
CZERNIN, J;MULLER, P;SCHELBERT, HR
通讯作者:
SCHELBERT, HR
影响因子:
37.8
作者:
BERGMANN, SR;HACK, S;SOBEL, BE
通讯作者:
SOBEL, BE
影响因子:
4.7
作者:
Kim, Dong-Yeon;Kim, Hee-Jung;Min, Jung-Joon
通讯作者:
Min, Jung-Joon
影响因子:
3.1
作者:
Kim, Dong-Yeon;Kim, Hee-Jung;Min, Jung-Joon
通讯作者:
Min, Jung-Joon