TY - JOUR
T1 - Brain accumulation of amyloid β protein visualized by positron emission tomography and BF-227 in Alzheimer's disease patients with or without diabetes mellitus
AU - Tomita, Naoki
AU - Furukawa, Katsutoshi
AU - Okamura, Nobuyuki
AU - Tashiro, Manabu
AU - Une, Kaori
AU - Furumoto, Shozo
AU - Iwata, Ren
AU - Yanai, Kazuhiko
AU - Kudo, Yukitsuka
AU - Arai, Hiroyuki
PY - 2013/1
Y1 - 2013/1
N2 - Aim: Although diabetes mellitus (DM) is considered to be one of the most consistent risks for developing dementia, it is not known if the pathology in dementia patients with DM is similar to or distinct from typical pathological features of Alzheimer's disease (AD). To discover the mechanism of developing dementia in AD patients with DM in a living state, we studied the distribution of amyloid β (Αβ) protein of diabetic AD patients. Methods: To evaluate the accumulation of Aβ, we examined 14 normal controls, four diabetic patients with AD and 11 non-diabetic patients with AD by positron emission tomography (PET) using BF-227, a currently developed Aβ tracer. Results: The analysis of PET images among the three groups showed an abundant aggregated Aβ accumulation in the cerebral cortex of both AD patients with and without DM. The extent and distributions of BF-227 accumulation in diabetic AD patients were not significantly different from these of non-diabetic AD patients. Conclusion: These results suggest that the degree and extent of Aβ deposition is not significantly different between AD with DM and AD alone.
AB - Aim: Although diabetes mellitus (DM) is considered to be one of the most consistent risks for developing dementia, it is not known if the pathology in dementia patients with DM is similar to or distinct from typical pathological features of Alzheimer's disease (AD). To discover the mechanism of developing dementia in AD patients with DM in a living state, we studied the distribution of amyloid β (Αβ) protein of diabetic AD patients. Methods: To evaluate the accumulation of Aβ, we examined 14 normal controls, four diabetic patients with AD and 11 non-diabetic patients with AD by positron emission tomography (PET) using BF-227, a currently developed Aβ tracer. Results: The analysis of PET images among the three groups showed an abundant aggregated Aβ accumulation in the cerebral cortex of both AD patients with and without DM. The extent and distributions of BF-227 accumulation in diabetic AD patients were not significantly different from these of non-diabetic AD patients. Conclusion: These results suggest that the degree and extent of Aβ deposition is not significantly different between AD with DM and AD alone.
KW - Alzheimer's disease
KW - Amyloid β-peptides
KW - Diabetes mellitus
KW - Positron emission tomography
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U2 - 10.1111/j.1447-0594.2012.00880.x
DO - 10.1111/j.1447-0594.2012.00880.x
M3 - Article
C2 - 22680403
AN - SCOPUS:84871971650
VL - 13
SP - 215
EP - 221
JO - Geriatrics and Gerontology International
JF - Geriatrics and Gerontology International
SN - 1447-0594
IS - 1
ER -