Laffon Eric, Marthan Roger
CHU de Bordeaux, Service de Médecine Nucléaire et Service d'Exploration Fonctionnelle Respiratoire, Hôpital du Haut-Lévèque, avenue de Magellan, F-33604 Pessac, France; Univ Bordeaux, Centre de Recherche Cardio-Thoracique de Bordeaux, INSERM U-1045, F-33000 Bordeaux, France; INSERM, Centre de Recherche Cardio-Thoracique de Bordeaux, U-1045, F-33000 Bordeaux, France.
CHU de Bordeaux, Service de Médecine Nucléaire et Service d'Exploration Fonctionnelle Respiratoire, Hôpital du Haut-Lévèque, avenue de Magellan, F-33604 Pessac, France; Univ Bordeaux, Centre de Recherche Cardio-Thoracique de Bordeaux, INSERM U-1045, F-33000 Bordeaux, France; INSERM, Centre de Recherche Cardio-Thoracique de Bordeaux, U-1045, F-33000 Bordeaux, France.
Nucl Med Biol. 2015 Sep;42(9):724-7. doi: 10.1016/j.nucmedbio.2015.04.006. Epub 2015 Apr 24.
The aim of this theoretic approach is to establish an analytical relationship between the total amount of uptake (TAU), either pathological or physiological, and the time constants "αi" that describe the time decay of the tracer input function (IF). The proposed approach uses parameters of a (population-based) arterial plasma IF for 18 F-FDG PET imaging.
A previously published formula provides an estimate of the ratio "p" of 18 F-FDG molecules that are irreversibly trapped in an 18 F-FDG-positive tissue during a whole PET examination, to the number of injected molecules. Then, the change in the magnitude of the IF time constants is derived, involving a corrective procedure.
Trapping of injected tracer molecules affects each αi that is increased by a factor of 1/(1-p), with p ranging between zero and, theoretically, less than 1. This result is illustrated in a patient showing an intense uptake in the mediastinum at initial staging of a diffuse large B-cell lymphoma (DLBCL).
An analytical relationship between TAU and the IF time constants is available in 18 F-FDG PET imaging, showing that TAU may actually affect the IF.
这种理论方法的目的是建立病理性或生理性摄取总量(TAU)与描述示踪剂输入函数(IF)时间衰减的时间常数“αi”之间的分析关系。所提出的方法使用基于人群的动脉血浆IF参数进行18F-FDG PET成像。
先前发表的一个公式可估算在整个PET检查期间不可逆地滞留在18F-FDG阳性组织中的18F-FDG分子与注射分子数量的比率“p”。然后,通过一个校正程序得出IF时间常数大小的变化。
注射示踪剂分子的滞留会影响每个αi,αi增大为1/(1-p)倍,其中p在零到理论上小于1的范围内。这一结果在一名弥漫性大B细胞淋巴瘤(DLBCL)初始分期时纵隔有强烈摄取的患者中得到了体现。
在18F-FDG PET成像中,TAU与IF时间常数之间存在分析关系,表明TAU实际上可能会影响IF。