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Full Text: 
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¿µ³²ÀÇ´ëÇмúÁö Yeungnam Univ J Med 2018;35(1):1-6
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REVIEW ARTICLE
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Beta-amyloid imaging in dementia |
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Kyung Ah Chun
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Department of Nuclear Medicine, Yeungnam University College of Medicine, Daegu, Korea
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Corresponding Author: Kyung Ah Chun, Department of
Nuclear Medicine, Yeungnam University College of
Medicine, 170, Hyeonchung-ro, Nam-gu, Daegu 42415,
Korea
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Tel: +82-53-620-3135, Fax: +82-53-620-3135
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E-mail: cka52@yumail.ac.kr
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Received: October 22, 2017, Revised: November 30, 2017
Accepted: January 3, 2018
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Abstract
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Alzheimer's disease (AD) is a neurodegenerative disorder associated with extracellular plaques, composed
of amyloid-beta (A¥â), in the brain. Although the precise mechanism underlying the neurotoxicity of A¥â has
not been established, A¥â accumulation is the primary event in a cascade of events that lead to neurofibrillary
degeneration and dementia. In particular, the A¥â burden, as assessed by neuroimaging, has proved to be
an excellent predictive biomarker. Positron emission tomography, using ligands such as 11C-labeled Pittsburgh
Compound B or 18F-labeled tracers, such as 18F-florbetaben, 18F-florbetapir, and 18F-flutemetamol,
which bind to A¥â deposits in the brain, has been a valuable technique for visualizing and quantifying the
deposition of A¥â throughout the brain in living subjects. A¥â imaging has very high sensitivity for detecting
AD pathology. In addition, it can predict the progression from mild cognitive impairment to AD, and contribute
to the development of disease-specific therapies.
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Key Words: Keywords: Alzheimer¡¯s disease; Amyloid-beta; Positron emission tomography
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