Radiation Dosimetry of β-Amyloid Tracers 11C-PiB and 18F-BAY94-9172

被引：67

作者：

O'Keefe, Graeme J. ^{[1
]}

Saunder, Timothy H. ^{[1
]}

Ng, Steven ^{[1
]}

Ackerman, Uwe ^{[1
]}

Tochon-Danguy, Henri J. ^{[1
]}

Chan, J. Gordon ^{[1
]}

Gong, Sylvia ^{[1
]}

Dyrks, Thomas ^{[2
]}

Lindemann, Stefanie ^{[2
]}

Holl, Gerhard ^{[2
]}

Dinkelborg, Ludger ^{[2
]}

Villemagne, Victor ^{[1
]}

Rowe, Christopher C. ^{[1
]}

机构：

[1] Austin Hosp, Ctr Positron Emiss Tomog, Heidelberg, Vic 3084, Australia

[2] Bayer Schering Pharma, Berlin, Germany

来源：

JOURNAL OF NUCLEAR MEDICINE | 2009年 / 50卷 / 02期

关键词：

PET; radiation dosimetry; (11)C-PiB; (18)F-BAY94-9172; ALZHEIMERS-DISEASE; IMAGING AGENTS; BIODISTRIBUTION; MEDICINE; PROTEIN; HUMANS;

D O I：

10.2967/jnumed.108.055756

中图分类号：

R8 [特种医学]; R445 [影像诊断学];

学科分类号：

1002 ; 100207 ; 1009 ;

摘要：

beta-Amyloid (A beta) imaging has great potential to aid in the diagnosis of Alzheimer disease and the development of therapeutics. The radiation dosimetry of A beta radioligands may influence their application; therefore, we calculated and compared the effective doses (EDs) of (11)C-PiB and a new (18)F-labeled ligand, (18)F-BAY94-9172. Methods: Attenuation-corrected whole-body scans were performed at 0, 15, 30, 45, and 60 min after injection of 350 +/- 28 MBq (mean +/- SD) of (11)C-PiB in 6 subjects and at 0, 20, 60, 120, and 180 min after injection of 319 +/- 27 MBq of (18)F-BAY94-9172 in 3 subjects. Coregistered CT was used to define volumes of interest (VOls) on the PET images. The source organs were the brain, lungs, liver, kidneys, spleen, and vertebrae. The VOls for the contents of the gallbladder, urinary bladder, lower large intestine, upper large intestine, and small intestine were also defined. Total activity in each organ at each time point was calculated by use of reference organ volumes. The resultant time-activity curves were fitted with constrained exponential fits, and cumulated activities were determined. A dynamic bladder voiding model was used. The OLINDA/EXM program was used to calculate the whole-body EDs from the acquired data. Results: For (11)C-PiB, the highest absorbed doses were in the gallbladder wall (44.80 +/- 29.30 mu Gy/mBq), urinary bladder wall (26.30 +/- 8.50 mu Gy/MBq), liver(19.88 +/- 3.58 mu Gy/MBq), and kidneys (12.92 +/- 3.37 mu Gy/MBq). The ED was 5.29 +/- 0.66 mu Sv/ MBq. For (18)F-BAY94-9172, the highest doses were also in the gallbladder wall (132.40 +/- 43.40 mu Gy/MBq), urinary bladder wall (24.77 +/- 7.36 mu Gy/MBq, and liver (39.07 +/- 8.31 mu Gy/ MBq). The ED was 14.67 +/- 1.39 mu Sv/MBq. Conclusion: The estimated organ doses for (11)C-PiB were comparable to those reported in earlier research. With the doses used in published studies (300-700 MBq), the EDs would range from 1.6 to 3.7 mSv. The ED of (18)F-BAY94-9172 was 30% lower than that of (18)F-FDG and, at the published dose of 300 MBq, would yield an ED of 4.4 mSv. The dosimetry of both A beta radioligands is suitable for clinical and research applications.

引用

页码：309 / 315

页数：7

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