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. Author manuscript; available in PMC: 2015 Oct 24.
Published in final edited form as: Lancet Neurol. 2010 Jan 8;9(2):149–158. doi: 10.1016/S1474-4422(10)70002-8

Figure 5. Disease-related metabolic patterns and post-mortem findings.

Figure 5

(A) The pattern related to idiopathic Parkinson’s disease (left)15 is characterised by increased (red areas) pallidothalamic and pontocerebellar metabolic activity associated with relative reductions (blue areas) in the premotor cortex, supplementary motor area, and parietal association regions. Neuropathological findings (right) from the substantia nigra pars compacta of a patient classified as having idiopathic Parkinson’s disease with a likelihood of 99% on the basis of fluorine-18-labelled-fluorodeoxyglucose (FDG)-PET 5·8 years before death. Diagnosis was confirmed at post-mortem examination, with the demonstration of Lewy-body containing neurons and severe cell loss in this region (LHE, 630X; top). Neuronal inclusions stained positively for α-synuclein (α-synuclein antibody, 400X; bottom). (B) The multiple system atrophy-related pattern (left)16 is characterised by bilateral metabolic reductions in putamen and cerebellar activity. Neuropathological findings (right) from a patient classified as having multiple system atrophy with a likelihood of 98% on the basis of FDG-PET 3 years before death. Autopsy revealed characteristic changes in abnormal hypometabolic pattern areas, with neuronal loss and gliosis in the putamen (top) and cerebellum (bottom). Both regions displayed glial cytoplasmic inclusions (Gallyas stain, 200X). Insets: putamen, 400X; cerebellum, 630X. (C) The progressive supranuclear palsy-related pattern (left)16 is characterised by metabolic reductions in the upper brainstem, medial frontal cortex, and medial thalamus. Neuropathological findings (right) from a patient classified as having progressive supranuclear palsy with a likelihood of 99% on the basis of FDG-PET 3·9 years before death. Post-mortem examination confirmed this diagnosis, with characteristic histopathological changes in abnormal hypometabolic pattern areas, in the pons (top) and frontal cortex (bottom). Argyrophilic globosum neuronal tangles were noted in the basis pontis (Bielschowsky stain 400X). A neuronal tangle with cytoplasmic inclusions and neuropil threads is displayed from the fifth cortical layer of the prefrontal region (AT8 stain, 630X). Tufted astrocytes (not shown) were present in this cortical region, the amygdala, globus pallidus, and claustrum. LHE=Luxol fast blue with haematoxylin and eosin.