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Table 2 Population based results from the pharmacokinetic analysis of FDG in arterial blood and (n=24) patients from Bern

From: Single time point quantitation of cerebral glucose metabolism by FDG-PET without arterial sampling

 

Aarhus (n = 52)

Bern (n = 24)

AUC(0–67), measured

100.0 ± 13.1

100.0 ± 12.3

Ce−λ3(t) (Method 1)

84.7 ± 3.9

83.6 ± 2.5

Be−λ2(t) + Ce−λ3(t)

95.5 ± 2.1

94.5 ± 1.6

Ae−λ1(t) + Be−λ2(t) + Ce−λ3(t)

98.7 ± 2.4

97.8 ± 2.1

Age (years)

56.5 ± 14.1

59.7 ± 15.2

λ3 (min−1)

0.0121 ± 0.0026

0.0094 ± 0.0019

theta(52–67 min) (min)

111.3 ± 9.8

100.8 ± 6.7

λ3 (min−1) versus age (years) (see Fig. 1C)

λ3 = − 0.0000936*(age) + 0.0174

(r = − 0.514; p > 0.0001)

λ3 = 0(age) + 0.00946

(r = − 0.011; not significant)

AUC(0–67 min) versus Ca(52–67)

(see Fig. 1D, Method 2)

AUC(0–67 min) = 63.2*(Ca(52–67 min)) + 374

(r =  + 0.678; p < 0.00001)

AUC(0–67 min) = 104.0(Ca(52–67)) + 2.9

(r = + 0.885; p < 0.00001

theta(52–67 min) (min) versus λ3 (min−1)

(see Fig. 1E, Method 3)

theta(52–67 min) = 2953*(λ3) + 75.57

(r =  + 0.796; p < 0.00001)

theta(52–67 min) = 2971(λ3) + 72.89

(r =  + 0.846; p < 0.00001)

theta(52–67 min) (min) versus age (years)

(see Fig. 1F, Method 4)

theta(52–67 min) = − 0.313*(age) + 129

(r = − 0.46; p < 0.0002)

theta(52–67 min) = 0.0477(age) + 98.0

(r =  + 0.17, n.s.)

  1. We obtained population-based results from the pharmacokinetics of FDG in arterial blood measured during PET recordings lasting 67 min, based on observations in (n = 52) patients from Aarhus and (n = 24) patients in Bern. The total measured AUC(0–67) was calculated from the IDIF measured during the complete dynamic recordings, and normalized to a mean of 100 arbitrary units of concentration-min. This AUC(0–67) is shown along with the percentage AUC recoveries from (1) the final phase of the tri-exponential function (ACe−λ3(t)), (2) the sum of the intermediate and final phases (Be−λ2(t) + Ce−λ3(t)), and (3) the complete tri-exponential function (Ae−λ1(t) + Be−λ2(t) + Ce−λ3(t)). We also report some relationships discovered for one or both sites, i.e., (1) the magnitude of λ3, which corresponds to renal clearance of FDG, versus subject age, (2) theta(55–67 min) versus λ3, AUC(0–67 min) versus Ca(52–67 min), and theta(52–67 min) versus subject age. Methods 1,2,3, and 4 refer to the specified empirical relationships for estimating the magnitude of FDG-Ki in brain from a two-point Patlak linear graphic analysis defined by (1) the population mean gray matter VD (0.55 ml g−1) and (2) estimations of AUC(0–67 min)/ theta(52–67 min) obtained from late phase recordings. In Method 1, we estimated the AUC(0–67) from the individual Ce−λ3(t)scaled by the population mean percentage AUC recoveries (84.7% in Aarhus, 83.6% in Bern). In Method 2, we estimated AUC(0–67) and thence theta(52–67 min) from the individual Ca(52–67 min) and the site-dependent empirical relationship. In Method 3, we estimated theta(52–67 min) from the individual λ3 based on the final 30 min of the recording and the site-dependent empirical relationship. In Method 4, we estimated theta(52–67 min) from the individual subject age and the site-dependent empirical relationship