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First published online November 15, 2007, 10.2967/jnumed.107.042820
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Journal of Nuclear Medicine Vol. 48 No. 12 1961-1970
© 2007 by Society of Nuclear Medicine

doi: 10.2967/jnumed.107.042820

Clinical Investigation

Comparison of 18F-FDG PET and Optimized Voxel-Based Morphometry for Detection of Alzheimer's Disease: Aging Effect on Diagnostic Performance

Ichiro Matsunari1, Miharu Samuraki2, Wei-Ping Chen1, Daiseke Yanase2, Nozomi Takeda1, Kenjiro Ono2, Mitsuhiro Yoshita2, Hiroshi Matsuda3, Masahito Yamada2 and Seigo Kinuya4

1 The Medical and Pharmacological Research Center Foundation, Hakui-city, Ishikawa, Japan; 2 Department of Neurology and Neurobiology of Aging, Kanazawa University Graduate School of Medical Science, Kanazawa, Japan; 3 Department of Nuclear Medicine, Saitama Medical School Hospital, Saitama, Japan; and 4 Department of Biotracer Medicine, Kanazawa University Graduate School of Medical Science, Kanazawa, Japan

Correspondence: For correspondence or reprints contact: Ichiro Matsunari, MD, PhD, The Medical and Pharmacological Research Center Foundation, Wo32, Inoyama-town, Hakui-city, Ishikawa 925-0613, Japan. E-mail: matsunari{at}mprcf.or.jp

The aim of this study was to compare optimized voxel-based morphometry (VBM) and 18F-FDG PET for discrimination between patients with Alzheimer's disease (AD) and healthy subjects in relation to age. Methods: The study population consisted of 2 groups; the first group (27 AD patients and 40 control subjects) was used to determine the locations of significant abnormalities for both PET and VBM using statistical parametric mapping, and the second group (34 AD patients and 50 control subjects) was used to compare the diagnostic performance of PET and VBM. In the second group, a z-score map for PET or VBM of each subject was obtained by comparison with the mean and SD of PET or gray-matter MR images of the control subjects. Receiver-operating-characteristic (ROC) curve analysis was then performed to compare the diagnostic performance between PET and VBM. Furthermore, group 2 was divided into the early- and late-onset subgroups, and ROC analysis was performed for each subgroup. Results: In the first group, VBM revealed a significant decrease in gray-matter concentration in the hippocampus complex in AD, whereas PET showed a significant reduction in 18F-FDG uptake in the posterior cingulate and parietotemporal lobe. The diagnostic performance of PET (0.988 ± 0.008; mean ± SE), as measured by the area under the ROC curve, was higher than that of VBM with (0.782 ± 0.059) or without (0.832 ± 0.049) modulation. PET yielded a sensitivity, specificity, and overall accuracy of 100%, 92%, and 95%, respectively, whereas for VBM the sensitivity, specificity, and accuracy were 74%, 92%, and 85%. Modulation for the VBM did not improve these values (56%, 94%, and 79%, respectively). When the early- and late-onset subjects were analyzed separately, the superiority of 18F-FDG PET was significant only in the early-onset subgroup. Conclusion: The present study indicates that the detection of metabolic alteration by 18F-FDG PET yields a better diagnostic performance for the discrimination between AD patients and healthy control subjects than does the morphologic approach by VBM, particularly in the early-onset subjects.

Key Words: 18F-FDG PET • voxel-based morphometry • Alzheimer's disease

COPYRIGHT © 2007 by the Society of Nuclear Medicine, Inc.


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