Optimization of methods for quantification of rCBF using high-resolution [ 15O]H 2O PET images

D. Walker*, M. Feldmann, C. Matthews, M. Anton-Rodriguez, S. Wang, J. Koepp, Asselin M-C Asselin, M. D. Walker, M. Feldmann, J. C. Matthews, J. M. Anton-Rodriguez, S. Wang, M. J. Koepp, M. C. Asselin

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

7 Citations (Scopus)

Abstract

This study aimed to derive accurate estimates of regional cerebral blood flow (rCBF) from noisy dynamic [ 15O]H 2O PET images acquired on the high-resolution research tomograph, while retaining as much as possible the high spatial resolution of this brain scanner (23 mm) in parametric maps of rCBF. The PET autoradiographic method and generalized linear least-squares (GLLS), with fixed or extended to include spatially variable estimates of the dispersion of the measured input function, were compared to nonlinear least-squares (NLLS) for rCBF estimation. Six healthy volunteers underwent two [ 15O]H 2O PET scans with continuous arterial blood sampling. rCBF estimates were obtained from three image reconstruction methods (one analytic and two iterative, of which one includes a resolution model) to which a range of post-reconstruction filters (3D Gaussian: 2, 4 and 6 mm FWHM) were applied. The optimal injected activity was estimated to be around 11 MBq kg 1 (800 MBq) by extrapolation of patient-specific noise equivalent count rates. Whole-brain rCBF values were found to be relatively insensitive to the method of reconstruction and rCBF quantification. The grey and white matter rCBF for analytic reconstruction and NLLS were 0.44 ± 0.03 and 0.15 ± 0.03 mL min 1 cm 3, respectively, in agreement with literature values. Similar values were obtained from the other methods. For generation of parametric images using GLLS or the autoradiographic method, a filter of >4 mm was required in order to suppress noise in the PET images which otherwise produced large biases in the rCBF estimates.

Original languageEnglish
Pages (from-to)2251-2271
Number of pages21
JournalPhysics in Medicine and Biology
Volume57
Issue number8
DOIs
Publication statusPublished - 21 Apr 2012
Externally publishedYes

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