Carluccio Giuseppe, Ding Yu-Shin, Logan Jean, Collins Christopher M
Department of Radiology, New York University, New York, NY, 10016, USA.
Med Phys. 2017 Feb;44(2):589-596. doi: 10.1002/mp.12046. Epub 2017 Jan 30.
To examine the possibility that MR-induced RF power deposition (SAR) and the resulting effects on temperature-dependent metabolic rates or perfusion rates might affect observed 18FDG signal in PET/MR.
Using numerical simulations of the SAR, consequent temperature increase, effect on rates of metabolism or perfusion, and [18FDG] throughout the body, we simulated the potential effect of maximum-allowable whole-body SAR for the entire duration of an hour-long PET/MR scan on observed PET signal for two different 18FDG injection times: one hour before onset of imaging and concurrent with the beginning of imaging. This was all repeated three times with the head, the heart, and the abdomen (kidneys) at the center of the RF coil.
Qualitatively, little effect of MR-induced heating is observed on simulated PET images. Maximum relative increases in PET signal (26% and 31% increase, respectively, for the uptake models based on metabolism and the perfusion) occur in regions of low baseline metabolic rate (also associated with low perfusion and, thus, greater potential temperature increase due to high local SAR), such that PET signal in these areas remains comparatively low. Maximum relative increases in regions of high metabolic rate (and also high perfusion: heart, thyroid, brain, etc.) are affected mostly by the relatively small increase in core body temperature and thus are not affected greatly (10% maximum increase).
Even for worst-case heating, little effect of MR-induced heating is expected on 18FDG PET images during PET/MR for many clinically relevant applications. For quantitative, dynamic MR/PET studies requiring high SAR for extended periods, it is hoped that methods like those introduced here can help account for such potential effects in design of a given study, including selection of reference locations that should not experience notable increase in temperature.
探讨磁共振成像(MR)诱导的射频功率沉积(比吸收率,SAR)以及由此对温度依赖性代谢率或灌注率产生的影响,是否可能影响正电子发射断层显像/磁共振成像(PET/MR)中观察到的18F-氟代脱氧葡萄糖(18FDG)信号。
通过对全身的SAR、随之的温度升高、对代谢率或灌注率的影响以及[18FDG]进行数值模拟,我们针对两种不同的18FDG注射时间,模拟了长达一小时的PET/MR扫描全过程中全身最大允许SAR对观察到的PET信号的潜在影响:成像开始前一小时注射和与成像开始同时注射。以头部、心脏和腹部(肾脏)位于射频线圈中心的情况,将上述过程重复三次。
定性地看,在模拟的PET图像上观察到MR诱导加热的影响很小。PET信号的最大相对增加(基于代谢和灌注的摄取模型分别增加26%和31%)出现在基线代谢率较低的区域(也与低灌注相关,因此由于局部高SAR导致温度升高的可能性更大),使得这些区域的PET信号仍然相对较低。高代谢率区域(以及高灌注区域:心脏、甲状腺、大脑等)的最大相对增加主要受核心体温相对较小的升高影响,因此影响不大(最大增加10%)。
即使在最坏的加热情况下,对于许多临床相关应用,在PET/MR期间MR诱导加热对18FDG PET图像的影响也预计很小。对于需要长时间高SAR的定量、动态MR/PET研究,希望本文介绍的方法能够有助于在特定研究设计中考虑这种潜在影响,包括选择温度不应显著升高的参考位置。