Positron emission tomography imaging in dementia
Abstract
Positron emission tomography (PET) is a well-established imaging modality. Measurement of regional cerebral glucose metabolism (rCMR(glc)) using PET and [(18)F]-2-fluoro-2-deoxy-D-glucose (FDG) has become a standard technique in both oncology and dementia research. When measuring rCMR(glc) in Alzheimer's disease (AD), characteristic reductions in rCMR(glc) are found in neocortical association areas including the posterior cingulate, precuneus, temporoparietal and frontal multimodal association regions; the primary visual cortex, sensorimotor cortex, basal ganglia and cerebellum are relatively unaffected. FDG-PET has been used in the study of mild cognitive impairment (MCI) to accurately predict the subsequent decline to AD. Impairment in rCMR(glc) may be seen in individuals at high genetic risk of AD, even before clinical symptoms are apparent. Characteristic patterns of regional hypometabolism are also seen in other degenerative dementias such as frontotemporal dementia (FTD) and dementia with Lewy bodies (DLB). The use of different radioisotopes and tracers increases the versatility of PET. Tracers adopted in dementia research include (11)C-PK-11195 and (11)C-PIB, which have been used to investigate neuroinflammation and amyloid deposition, respectively, in both AD and MCI populations. It is also possible to investigate neurotransmitter systems in dementia; targets have included the cholinergic, dopaminergic and serotonergic systems. Imaging the brains of dementia patients…
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TSPO-binding radioligands used to assess neuroinflammation via PET imaging may have value as a biosensor of ongoing disease and may also be a target to reduce inflammation-mediated damage in diseases such as HIV-associated neurological disorders and dementia.
“Use of TSPO-binding radioligands to assess neuroinflammation via PET imaging indicates that they may have value as a biosensor of ongoing disease and may also be a target to reduce inflammation-mediated damage in diseases such as HIV-associated neurological disorders and dementia ([17] and see [15;18] for review).”
From Expression of the translocator protein of 18 kDa by microglia, macrophages and astrocytes based on immunohistochemical localization in abnormal human brain (2009) · cites this paper as [17]
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References 117 · Cited by 287
- Authors
- HERHOLZ, K., CARTER, S. F., & JONES, M.
- Affiliations
- University of Manchester (GB)
- Venue
- The British Journal of Radiology
- Publisher
- Oxford University Press (OUP)
- Published
- 2007-12
- Volume
- 80
- Issue
- special_issue_2
- Pages
- S160-S167
- ISSN
- 0007-1285 (ISSN-L)
- 1748-880X
- OpenAlex
- W2131406087
- Cited by
- 287
- References
- 117
- Citations by year
- 2026: 3 · 2025: 6 · 2024: 9 · 2023: 6 · 2022: 6 · 2021: 10 · 2020: 37 · 2019: 11 · 2018: 8 · 2017: 7 · 2016: 26 · 2015: 13 · 2014: 18 · 2013: 26 · 2012: 21
- FWCI
- 2.46
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- British Journal of Radiology (publishedVersion)
- PubMed (publishedVersion)
- Research Explorer (The University of Manchester) (publishedVersion)
- Topics
- Health Sciences › Medicine › Psychiatry and Mental health › Dementia and Cognitive Impairment Research
- Health Sciences › Medicine › Radiology, Nuclear Medicine and Imaging › Medical Imaging Techniques and Applications
- Health Sciences › Medicine › Physiology › Alzheimer's disease research and treatments
- Keywords
- positron emission tomography, dementia, Alzheimer's disease, regional cerebral glucose metabolism, FDG-PET, mild cognitive impairment, frontotemporal dementia, dementia with Lewy bodies, neuroinflammation, amyloid deposition, PK11195, Pib, neurotransmitter systems, cholinergic system, dopaminergic system, serotonergic system, early diagnosis
- MeSH terms
- Alzheimer Disease, Blood Glucose, Brain, Cognition Disorders, Dementia, Humans, Neurotransmitter Agents, Radiopharmaceuticals, Fluorodeoxyglucose F18, Lewy Body Disease, Positron-Emission Tomography
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