SPECT and PET imaging in Alzheimer’s disease

Alzheimer’s disease (AD) is a progressive neurodegenerative disorder and the most common cause of dementia. Beta-amyloid (Aβ) deposition and neurofibrillary tangles (NFTs) of abnormal hyperphosphorylated tau protein are the pathological hallmarks of the disease, accompanied by other pathological pro...

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Published inAnnals of nuclear medicine Vol. 32; no. 9; pp. 583 - 593
Main Authors Valotassiou, Varvara, Malamitsi, Julia, Papatriantafyllou, John, Dardiotis, Efthimios, Tsougos, Ioannis, Psimadas, Dimitrios, Alexiou, Sotiria, Hadjigeorgiou, George, Georgoulias, Panagiotis
Format Journal Article
LanguageEnglish
Published Tokyo Springer Japan 01.11.2018
Springer Nature B.V
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Summary:Alzheimer’s disease (AD) is a progressive neurodegenerative disorder and the most common cause of dementia. Beta-amyloid (Aβ) deposition and neurofibrillary tangles (NFTs) of abnormal hyperphosphorylated tau protein are the pathological hallmarks of the disease, accompanied by other pathological processes such as microglia activation. Functional and molecular nuclear medicine imaging with single-photon emission computed tomography (SPECT) and positron emission tomography (PET) techniques provides valuable information about the underlying pathological processes, many years before the appearance of clinical symptoms. Nuclear neuroimaging in AD has made great progress in the past two decades and has extended beyond the traditional role of brain perfusion and glucose metabolism evaluation. Intense efforts in radiopharmaceuticals research have led to the development of various probes able to detect Aβ deposits, tau protein accumulation, microglia activation and neuroinflammation. As a result, SPECT and PET have proposed to serve as biomarkers in recently revised diagnostic clinical criteria for the early diagnosis of AD and the prediction of progression to AD in mild cognitive impairment (MCI) subjects.
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ISSN:0914-7187
1864-6433
1864-6433
DOI:10.1007/s12149-018-1292-6