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Journal of Nuclear Medicine

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Meeting ReportNeurosciences: Neurology

Early C-11-PIB distribution as perfusion index for differential diagnosis in dementia: A comparison with F-18-FDG-PET

Matthias Reimold, Walter Mätzler, Inga Liepelt-Scarfone, Gerald Reischl and Roland Bares
Journal of Nuclear Medicine May 2011, 52 (supplement 1) 1253;
Matthias Reimold
1Nuclear Medicine, University of Tuebingen, Tuebingen, Germany
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Walter Mätzler
3Neurology, University of Tuebingen, Tuebingen, Germany
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Inga Liepelt-Scarfone
3Neurology, University of Tuebingen, Tuebingen, Germany
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Gerald Reischl
2Radiopharmacy, University of Tuebingen, Tuebingen, Germany
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Roland Bares
1Nuclear Medicine, University of Tuebingen, Tuebingen, Germany
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Abstract

1253

Objectives Cerebral amyloid load and patterns of hypometabolism/-perfusion are complementary information in differential diagnosis of dementia. Due to a high extraction fraction, early distribution of the amyloid ligand C-11-PIB reflects tissue perfusion with good signal-to-noise ratio. Our aim was to exploratively evaluate the diagnostic potential of early PIB distribution by intraindividual comparison with F-18-FDG uptake.

Methods 4 pts. with Alzheimer's disease (AD), 8 pts. with dementia with lewy bodies (DLB) and 12 controls underwent PIB- and FDG-PET (max. 800MBq PIB and 370MBq FDG). Tracer concentration 0 to 4min p.i. (PIB) and 40 to 52min p.i. (FDG) were coregistered, spatially normalized (SPM2), smoothed (12mm) and scaled using a wholebrain-ROI. For each pat., two z-images (FDG and PIB) were calculated from voxelwise comparison with the control group. Each pair of z-images was rated visually. Furthermore, we calculated for each pat. the percentage volume with which clusters of reduced tracer concentration overlapped (100% = cluster size at FDG-z>2.5).

Results The hypometabolic volume (FDG:z>2.5) ranged from 60 to 225ml per pat.. 56% (median across pts.) of the respective voxels also showed PIB-reductions (z>2). The extent of PIB reductions (z>2.5) outside the FDG-cluster (z>2) was only 10% (median). The largest mismatch was found in a DLB pat. with moderate temporooccipital hypometabolism not evident in PIB (overlap: 32%). In patients with clear-cut hypometabolism, z-images from PIB- and FDG-PET were rated equivalent.

Conclusions In AD and DLB with clear-cut hypometabolism, early PIB distribution seems to be of equal diagnostic value as FDG-uptake and may support clinical diagnosis if an FDG scan is not available. Generally, findings in PIB-perfusion tended to be of lower significance than in FDG-PET, however, there might be room for further optimizing PIB-quantification for diagnostic purposes (reference tissue? modelling?)

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Journal of Nuclear Medicine
Vol. 52, Issue supplement 1
May 2011
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Early C-11-PIB distribution as perfusion index for differential diagnosis in dementia: A comparison with F-18-FDG-PET
Matthias Reimold, Walter Mätzler, Inga Liepelt-Scarfone, Gerald Reischl, Roland Bares
Journal of Nuclear Medicine May 2011, 52 (supplement 1) 1253;

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Early C-11-PIB distribution as perfusion index for differential diagnosis in dementia: A comparison with F-18-FDG-PET
Matthias Reimold, Walter Mätzler, Inga Liepelt-Scarfone, Gerald Reischl, Roland Bares
Journal of Nuclear Medicine May 2011, 52 (supplement 1) 1253;
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