RT Journal Article SR Electronic T1 Movement Correction Method for Human Brain PET Images: Application to Quantitative Analysis of Dynamic 18F-FDDNP Scans JF Journal of Nuclear Medicine JO J Nucl Med FD Society of Nuclear Medicine SP 210 OP 218 DO 10.2967/jnumed.109.063701 VO 51 IS 2 A1 Mirwais Wardak A1 Koon-Pong Wong A1 Weber Shao A1 Magnus Dahlbom A1 Vladimir Kepe A1 Nagichettiar Satyamurthy A1 Gary W. Small A1 Jorge R. Barrio A1 Sung-Cheng Huang YR 2010 UL http://jnm.snmjournals.org/content/51/2/210.abstract AB Head movement during a PET scan (especially a dynamic scan) can affect both the qualitative and the quantitative aspects of an image, making it difficult to accurately interpret the results. The primary objective of this study was to develop a retrospective image-based movement correction (MC) method and evaluate its implementation on dynamic 2-(1-{6-[(2-18F-fluoroethyl)(methyl)amino]-2-naphthyl}ethylidene)malononitrile (18F-FDDNP) PET images of cognitively intact controls and patients with Alzheimer's disease (AD). Methods: Dynamic 18F-FDDNP PET images, used for in vivo imaging of β-amyloid plaques and neurofibrillary tangles, were obtained from 12 AD patients and 9 age-matched controls. For each study, a transmission scan was first acquired for attenuation correction. An accurate retrospective MC method that corrected for transmission–emission and emission–emission misalignments was applied to all studies. No restriction was assumed for zero movement between the transmission scan and the first emission scan. Logan analysis, with the cerebellum as the reference region, was used to estimate various regional distribution volume ratio (DVR) values in the brain before and after MC. Discriminant analysis was used to build a predictive model for group membership, using data with and without MC. Results: MC improved the image quality and quantitative values in 18F-FDDNP PET images. In this subject population, no significant difference in DVR value was observed in the medial temporal (MTL) region of controls and patients with AD before MC. However, after MC, significant differences in DVR values in the frontal, parietal, posterior cingulate, MTL, lateral temporal (LTL), and global regions were seen between the 2 groups (P < 0.05). In controls and patients with AD, the variability of regional DVR values (as measured by the coefficient of variation) decreased on average by more than 18% after MC. Mean DVR separation between controls and patients with AD was higher in frontal, MTL, LTL, and global regions after MC. Group classification by discriminant analysis based on 18F-FDDNP DVR values was markedly improved after MC. Conclusion: The streamlined and easy-to-use MC method presented in this work significantly improves the image quality and the measured tracer kinetics of 18F-FDDNP PET images. The proposed MC method has the potential to be applied to PET studies on patients having other disorders (e.g., Down syndrome and Parkinson's disease) and to brain PET scans with other molecular imaging probes.