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First published online May 14, 2009, 10.2967/jnumed.108.058529
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Journal of Nuclear Medicine Vol. 50 No. 6 878-886
© 2009 by Society of Nuclear Medicine

doi: 10.2967/jnumed.108.058529

Clinical Investigation

Comparison of 18F-FDG and PiB PET in Cognitive Impairment

Val J. Lowe1, Bradley J. Kemp1, Clifford R. Jack, Jr.1, Matthew Senjem2, Stephen Weigand3, Maria Shiung1, Glenn Smith4, David Knopman5, Bradley Boeve5, Brian Mullan1 and Ronald C. Petersen5

1 Department of Radiology, Mayo Clinic, Rochester, Minnesota; 2 Department of Information Technology, Mayo Clinic, Rochester, Minnesota; 3 Department of Health Sciences Research, Mayo Clinic, Rochester, Minnesota; 4 Department of Psychology, Mayo Clinic, Rochester, Minnesota; and 5 Department of Neurology, Mayo Clinic, Rochester, Minnesota

Correspondence: For correspondence or reprints contact: Val J. Lowe, Mayo Clinic, 200 First St. SW, Rochester, MN 55905. E-mail: vlowe{at}mayo.edu

The purpose of this study was to compare the diagnostic accuracy of glucose metabolism and amyloid deposition as demonstrated by 18F-FDG and Pittsburg Compound B (PiB) PET to evaluate subjects with cognitive impairment. Methods: Subjects were selected from existing participants in the Mayo Alzheimer's Disease Research Center or Alzheimer's Disease Patient Registry programs. A total of 20 healthy controls and 17 amnestic mild cognitive impairment (aMCI), 6 nonamnestic mild cognitive impairment (naMCI), and 13 Alzheimer disease (AD) subjects were imaged with both PiB and 18F-FDG PET between March 2006 and August 2007. Global measures for PiB and 18F-FDG PET uptake, normalized to cerebellum for PiB and pons for 18F-FDG, were compared. Partial-volume correction, standardized uptake value (SUV), and cortical ratio methods of image analysis were also evaluated in an attempt to optimize the analysis for each test. Results: Significant discrimination (P < 0.05) between controls and AD, naMCI and aMCI, naMCI and AD, and aMCI and AD by PiB PET measurements was observed. The paired groupwise comparisons of the global measures demonstrated that PiB PET versus 18F-FDG PET showed similar significant group separation, with only PiB showing significant separation of naMCI and aMCI subjects. Conclusion: PiB PET and 18F-FDG PET have similar diagnostic accuracy in early cognitive impairment. However, significantly better group discrimination in naMCI and aMCI subjects by PiB, compared with 18F-FDG, was seen and may suggest early amyloid deposition before cerebral metabolic disruption in this group.

Key Words: PET • dementia • 18F-FDG • PiB

COPYRIGHT © 2009 by the Society of Nuclear Medicine, Inc.


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