Background
l-Methyl-[
11C]methionine (MET) is a useful radiotracer in positron emission tomography (PET) conducted for the diagnosis of tumors [
1‐
20]. In particular, MET PET has been shown to enable reliable diagnosis of brain tumors because of the low physiologic uptake of MET in the brain. It has been reported that the extent of tumor cell invasion can be detected more clearly by MET PET than by computed tomography (CT) or MRI [
2‐
5,
21]. MET PET has also been used to evaluate amino acid metabolism in the pancreas and liver and, recently, also in the myocardium [
22‐
26]. However, the study protocol for MET PET has not yet been standardized. For example, the reported scan initiation time after MET injection is variable, ranging from 15 to 30 min (Table
1) [
1‐
13,
18,
24,
25]. Moreover, the concentrations of neutral amino acids (NAAs) in the plasma were not measured, despite the possibility of these affecting the tracer MET uptake by tissues in a competitive way. Although the NAA concentrations in the plasma were found to be influenced when measured after a meal, a fasting period before MET PET study has not been suggested. The purpose of this study was to confirm previous published protocols and standardize the scan initiation times of MET PET for various organs. We also examined the effects of the NAA concentrations in the plasma on the standardized uptake values (SUVs) in the MET PET study.
Table 1
Summary of the scan initiation times after intravenous injection of MET
| Brain | No | 20 | 250 to 500 |
| Brain | ≧4 | 20 | 370 to 720 |
| Brain | No | 23 | 740 |
| Brain | No | 20 | 740 |
| Head and neck | ≧4 | 23 | 374 to 870 |
| Thyroid | ≧6 | 30 | 740 |
| Parathyroid gland | 3 | 15 to 20 | 272 to 603 |
| Cardiac tissue | 6 | 20 | 370 |
| Lung | ≧5 | 15 to 20 | 361 to 607 |
| Lung | ≧6 | 15 to 30 | 296 to 555 |
| Breast | ≧4 | 20 to 35 | 220 to 370 |
| Thymus | ≧6 | 15 | 70 to 818 |
| Pancreas | No | 6 to 8 | 370 to 740 |
| Pancreas | 6 | 30 | 370 to 740 |
| Pelvis | ≧6 | 23 | 740 |
| Prostate | Time unknown | 20 | 3 MBq/kg |
| Bone marrow | 5 to 8 | 20 | 1,000 ± 0.2 (SD) |
Methods
Subjects
A total of 11 healthy volunteers (Japanese, nine males and two females) participated in the present study after receiving a detailed explanation on the radiotracer drug and the purpose and contents of the study. This study was performed with the approval of the institutional ethics committee for clinical research of Osaka University. Written informed consent was obtained from all the subjects.
The mean age of the 11 subjects was 24.4 years (range, 24 to 26 years), and the mean height and weight were 168.45 cm (range, 154 to 176 cm) and 59.45 kg (range, 50 to 78 kg), respectively. None of the subjects had a prior history of any major medical illness.
Administration of the MET and PET imaging protocol
All subjects fasted for at least 4 h before the radiotracer injection and underwent blood laboratory tests for NAA densitometry and sequential whole-body MET PET-CT (Gemini GXL, Philips, Cleveland, OH, USA) in the three-dimensional acquisition mode. The scanner provides 220 continuous transaxial slices with a spatial resolution of 5.3 mm full width at half maximum in the axial direction. The axial field of view is 18 cm. Whole-body low-dose CT for attenuation correction was performed at the beginning of each imaging session. Thereafter, MET (370 MBq/50 kg) was injected as a bolus into the antecubital vein. Repeated whole-body PET scan of the marked area was initiated at the time of the tracer injection. Seven repeated whole-body PET scans from the parietal crown to the groin were performed in each of ten healthy volunteers, and six repeated whole-body PET scans were performed in one healthy volunteer. The data consisted of nine-frame scan with 30-s acquisition time for each frame, and the interval between scans was set at 122 s. Decay of radioactivity during PET scan was corrected to the time of initiation of the first scan. PET reconstruction algorithms were the line-of-response row-action maximum likelihood algorithm (RAMLA) and 3D RAMLA.
Evaluation of the biodistribution
The radioactivities in various source organs were obtained from reconstructed PET images by averaging the activities (cps/ml) in the regions of interest (ROIs) in each organ since the radioactivity distribution within an organ can be considered uniform [
27]. ROIs were manually located on each organ by tracing the MET activity on the PET images, and the maximal standardized uptake value (SUV max) at every mid-scan time was evaluated in various organs by setting ROIs on the whole-body PET-CT images. All the PET counts were corrected for physical decay of
11C (T1/2 = 20.4 min). Circular ROIs with a diameter 16 to 32 mm were drawn on tomographic images within the brain, parotid, lung, myocardium, ventricular blood pool, stomach, spleen, liver, pancreas, right kidney, right and left intestine, the urine in the urinary bladder, muscle, and bone marrow, and on tomographic images within the prostate in the male subjects and the breast and corpus uteri in the female subjects. Regarding the bone marrow, the ROI was set and measured to the fifth lumbar body that an anatomical position tends to identify. Time-activity curves in 18 source organs were obtained from the six or seven repeated whole-body PET measurements.
Measurement of NAA concentrations in the plasma
In all subjects, the NAA concentrations in the plasma were measured after the subjects had fasted for 4 h before the PET study. The venous sampling just before the PET study was submitted and measured by the SRL company. The amino acids measured were methionine, phenylalanine, tryptophan, isoleucine, leucine, valine, threonine, tyrosine, and histidine, which are transported through the same carrier termed the L-system, as methionine [
28]. The affinities of the carrier system for these nine NAAs are different. When the affinity ratio of methionine to the nine NAAs is defined as Km(i)/Km, where Km is the half-saturation constant for methionine and Km(i) is the half-saturation constant for each NAA, the concentration Ci of each NAA divided by the Km(i)/Km is the concentration corresponding to methionine for the NAA carrier system. The sum of Ci/(Km(i)/Km) for the nine NAAs, a weighted sum of the NAAs (C’), is the methionine-equivalent concentration of the nine NAAs for the carrier system. The Km(i) in the rat brain was used as follows: methionine 0.040, phenylalanine 0.011, tryptophan 0.015, isoleucine 0.056, leucine 0.029, valine 0.21, threonine 0.22, tyrosine 0.040, and histidine 0.100 (μmole/ml) [
29]. The weighted sum of the plasma concentrations of the NAAs determined after the volunteers had fasted for 4 h was calculated and examined in relation to the SUV max of each organ in the fourth scanning at 19.6 to 24.1 min.
Statistical analysis
The relationship between the SUV max of each organ in the fourth scanning at 19.6 to 24.1 min and the weighted sum of the plasma concentrations of the NAAs determined after the volunteers had fasted for 4 h was analyzed in every part with linear regression and Spearman correlation tests. In all statistical analyses, significance was defined as a P value less than 0.05. Statistical analysis was performed with StatMate IV (ATMS Co., Ltd., Tokyo, Japan).
Discussion
The present study revealed dynamic changes in the radioactivity in the whole body for 43.7 min after MET infusion in normal volunteers. The radioactivity reached a plateau within 6.5 to 11 min in the pancreas and within 19.6 to 24.1 min in the brain, lung, and myocardium. The radioactivity, as represented by the SUVs, was not affected by the NAA concentrations in the plasma if the PET study was conducted in the subjects after a fasting period of 4 h.
In the 2-[
18F]fluoro-2-deoxy-D-glucose (FDG) PET study, while the SUVs decline in normal tissues in the post-injection period, those in tumors generally increase, indicating that the SUVs of normal and tumor tissues are dependent on the time of scan initiation after infusion. Therefore, it is important to initiate the scanning at a consistent time-point after the FDG injection. The SNM procedure guidelines for tumor PET imaging recommended that emission images should be obtained at least 45 min after injection of the radiopharmaceutical [
30]. The EANM procedure guidelines for tumor PET imaging recommended a 60-min interval between FDG administration and the start of image acquisition [
31]. In contrast, MET accumulation in MET PET reaches a plateau in most normal organs. The MET accumulation in brain tumors and lung cancers also reached a plateau at 5 to 10 min after the radiotracer injection [
32,
33]. These findings imply that after the plateau phase is reached, the SUVs of normal tissues and tumors in MET PET might be independent of the scan initiation time. In most previous studies, the scanning was initiated 15 min or later after MET injection (Table
1). Therefore, in accordance with the above idea, their SUV values were consistent, despite the differing scan initiation times. It is noteworthy that the SUV values of brain tumors and lung cancers measured at 20 min after MET injection were significantly correlated with the uptake values estimated by repeated PET scan after MET infusion, metabolite-corrected arterial input function, and graphic analysis [
34].
The radioactivity half-life of MET is short, being 20.4 min. If the PET scan can be initiated earlier than this time after injection of MET, high radioactivity can be expected, and much information can be acquired. Even with small doses of MET, a large number of patients can be evaluated by MET PET-CT within a short time. This also leads to reduction of the patient’s exposure to radioactivity. Our results show that MET PET scanning for evaluating the aforementioned targeted organs may be started 20 min or later after injection of MET. However, even if SUV levels are not stable in all organs, in several organs such as the pancreas, spleen, and kidney, the scan initiation from 15 min later does not seem to become the problem.
Another factor influencing the SUVs of MET is the plasma concentrations of NAAs. [
11C]MET is transported through the NAA transporter from the plasma to the tissues. Therefore, plasma NAA concentrations could affect the uptake of [
11C]MET in a competitive fashion. Ito et al. reported that brain uptake of the NAA tracer [
18F]fluorophenylalanine was inversely correlated with the plasma NAA concentrations [
29]. However, no previous studies have investigated the effects of plasma NAA concentrations on [
11C]MET accumulation in the target tissues. In this study, we did not find a significant effect of the plasma methionine-equivalent concentrations on the MET uptake. This is considered to be due to the fact that in our subjects, the NAA concentrations in the plasma returned within normal range after a fasting period of 4 h (525.2 to 1,025.2 nmol/ml). On the other hand, Ito et al. did not set a fasting period prior to the study [
29]. Four of the 14 patients in their study showed plasma NAA concentrations outside the normal ranges.
There are two limitations to this study. First, though blood clearance was one of the important factors for determining the best timing of scan initiation, we did not take blood samples and measure their radioactivities during the scan. We carefully set and measured ROI in the left ventricle blood pool instead and confirmed that blood clearance was rapid. Second, [18F]fluorophenylalanine mainly recognizes amino acid transport but is not metabolized in the cell, while MET is metabolized in the cells after transportation. The difference may affect the effect of NAA on tissue MET uptake.
Acknowledgments
The authors thank the staff of the Department of Nuclear Medicine, Osaka University Hospital for their assistance. This work was supported in part by Grants-in-Aid for Scientific Research (S) (2429008), for Scientific Research (C) (24591758, 23592089), and for Young Scientists (B) (23701083, 23791420, 24791301), from the Ministry of Education, Culture, Sports, Science and Technology, Japan.
Competing interests
The authors declare that they have no competing interests.
Authors’ contributions
KI, ES, and JH participated in the design of the study and performed the statistical analysis. Data acquisition was done by KI, ES, YK, SN, and KF. Data analysis was done by KI, HK, and HW. The manuscript was prepared by KI. All authors read and approved the final manuscript.