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  1. 原著論文

Amyloid and Tau Positron Emission Tomography in Suggested Diabetesrelated Dementia

https://repo.qst.go.jp/records/49185
https://repo.qst.go.jp/records/49185
ef429c7e-f658-425b-b5a8-3e3ba78c8059
Item type 学術雑誌論文 / Journal Article(1)
公開日 2018-09-28
タイトル
タイトル Amyloid and Tau Positron Emission Tomography in Suggested Diabetesrelated Dementia
言語
言語 eng
資源タイプ
資源タイプ識別子 http://purl.org/coar/resource_type/c_6501
資源タイプ journal article
アクセス権
アクセス権 metadata only access
アクセス権URI http://purl.org/coar/access_right/c_14cb
著者 Takenoshita, Naoto

× Takenoshita, Naoto

WEKO 865091

Takenoshita, Naoto

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Fukasawa, Raita

× Fukasawa, Raita

WEKO 865092

Fukasawa, Raita

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Ogawa, Yusuke

× Ogawa, Yusuke

WEKO 865093

Ogawa, Yusuke

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Shimizu, Soichiro

× Shimizu, Soichiro

WEKO 865094

Shimizu, Soichiro

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Umahara, Takahiko

× Umahara, Takahiko

WEKO 865095

Umahara, Takahiko

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Ishii, Kenji

× Ishii, Kenji

WEKO 865096

Ishii, Kenji

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Shimada, Hitoshi

× Shimada, Hitoshi

WEKO 865097

Shimada, Hitoshi

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Higuchi, Makoto

× Higuchi, Makoto

WEKO 865098

Higuchi, Makoto

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Suhara, Tetsuya

× Suhara, Tetsuya

WEKO 865099

Suhara, Tetsuya

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Hanyu, Haruo

× Hanyu, Haruo

WEKO 865100

Hanyu, Haruo

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Shimada, Hitoshi

× Shimada, Hitoshi

WEKO 865101

en Shimada, Hitoshi

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Higuchi, Makoto

× Higuchi, Makoto

WEKO 865102

en Higuchi, Makoto

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Suhara, Tetsuya

× Suhara, Tetsuya

WEKO 865103

en Suhara, Tetsuya

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抄録
内容記述タイプ Abstract
内容記述 Abstract: Background: Type 2 diabetes mellitus (DM) has been shown to increase the risk for cognitive
decline and dementia, such as Alzheimer disease (AD) and vascular dementia (VaD). In addition to
AD and VaD, there may be a dementia subgroup associated with specific DM-related metabolic abnormalities
rather than AD pathology or cerebrovascular disease, referred to as diabetes-related dementia
(DrD).
Method: We studied 11C-PiB and 11C-PBB3 positron emission tomography (PET) in 31 subjects with
DrD and 5 subjects with AD associated with DM to assess amyloid and tau deposits in the brain.
Results: All subjects with AD showed both positive PiB and PBB3. However, only 12 out of 31 subjects
(39%) with DrD showed positive PiB, whereas 17 out of 21 subjects (81%) who underwent PBB3 PET
showed positive PBB3. Depending on the positivity of PiB and PBB3, we classified 21 subjects into a
negative PiB and a positive PBB3 pattern (11 cases, 52%), indicating tauopathy, a positive PiB and a
positive PBB3 pattern (6 cases, 29%), indicating AD pathology, or a negative PiB and a negative PBB3
pattern (4 cases, 19%). Among 11 subjects showing a negative PiB and a positive PBB3 pattern, there
were 2 PBB3 deposit patterns, including the medial temporal lobe only and extensive neocortex beyond
the medial temporal lobe.
Conclusion: DrD showed variable amyloid and tau accumulation patterns in the brain. DrD may be associated
predominantly with tau pathology, in addition to AD pathology and non-amyloid/non-tau neuronal
damage due to DM-related metabolic abnormalities.
書誌情報 Current Alzheimer Research

巻 15, 号 11, p. 1062-1069, 発行日 2018-07
出版者
出版者 Bentham Science Publishers
ISSN
収録物識別子タイプ ISSN
収録物識別子 1567-2050
PubMed番号
識別子タイプ PMID
関連識別子 29984653
DOI
識別子タイプ DOI
関連識別子 10.2174/1567205015666180709113338
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