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Tau deposition estimated by [11C]PBB3 PET in Alzheimer’s disease, MCI with and without amyloid deposition, and cognitive healthy subjects

https://repo.qst.go.jp/records/65627
https://repo.qst.go.jp/records/65627
a8106593-13d5-4375-8107-d957993c47fb
Item type 会議発表用資料 / Presentation(1)
公開日 2015-04-20
タイトル
タイトル Tau deposition estimated by [11C]PBB3 PET in Alzheimer’s disease, MCI with and without amyloid deposition, and cognitive healthy subjects
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_c94f
資源タイプ conference object
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 Shimada, Hitoshi

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WEKO 646385

Shimada, Hitoshi

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Higuchi, Makoto

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WEKO 646386

Higuchi, Makoto

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Shinotoh, Hitoshi

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WEKO 646387

Shinotoh, Hitoshi

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Furukawa, Shogo

× Furukawa, Shogo

WEKO 646388

Furukawa, Shogo

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Eguchi, Yoko

× Eguchi, Yoko

WEKO 646389

Eguchi, Yoko

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Takahata, Keisuke

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WEKO 646390

Takahata, Keisuke

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Kodaka, Fumitoshi

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WEKO 646391

Kodaka, Fumitoshi

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Kimura, Yasuyuki

× Kimura, Yasuyuki

WEKO 646392

Kimura, Yasuyuki

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Yamada, Makiko

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WEKO 646393

Yamada, Makiko

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Sahara, Naruhiko

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WEKO 646394

Sahara, Naruhiko

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Maruyama, Masahiro

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WEKO 646395

Maruyama, Masahiro

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Takano, Harumasa

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WEKO 646396

Takano, Harumasa

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Zhang, Ming-Rong

× Zhang, Ming-Rong

WEKO 646397

Zhang, Ming-Rong

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Ito, Hiroshi

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WEKO 646398

Ito, Hiroshi

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Suhara, Tetsuya

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Suhara, Tetsuya

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島田 斉

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en 島田 斉

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樋口 真人

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en 樋口 真人

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篠遠 仁

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en 篠遠 仁

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古川 彰吾

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江口 洋子

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en 江口 洋子

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高畑 圭輔

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en 高畑 圭輔

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小高 文聰

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en 小高 文聰

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木村 泰之

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WEKO 646407

en 木村 泰之

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山田 真希子

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WEKO 646408

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佐原 成彦

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丸山 将浩

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高野 晴成

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張 明栄

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伊藤 浩

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須原 哲也

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抄録
内容記述タイプ Abstract
内容記述 Background and aims:
[11C]PBB3 is a novel tau imaging PET ligand, showing high affinity and selectivity for tau deposits. Our preliminary clinical data suggested [11C]PBB3 binding could reflect the dementia severity in AD patients. The aim of the present study was to investigate characteristics of [11C]PBB3 binding and its relation with clinical aspects in cognitively healthy subjects and patients with cognitive impairments.
Methods:
Participants were 14 AD patients, 13 mild cognitive impairments (MCI) patients and 22 healthy controls (HCs). We performed [11C]PBB3 PET as well as [11C]PIB PET. Standardized uptake value ratio (SUVR) was calculated for each PET image using the cerebellar cortex as reference region. Three-dimensional T1-weighted MRI was also acquired, and brain atrophy was also assessed using voxel-based morphometry technique.
Results:
All HCs were PIB-negative, and all AD patients and 7 of 13 MCI patients were PIB-positive. [11C]PBB3 was highly accumulated in the medial temporal cortex of all AD and PIB-positive MCI patients, in which binding of [11C]PIB was minimal. Distribution of [11C]PBB3 accumulation observed in AD and PIB-positive MCI patients extended to the entire limbic system and subsequently to the neocortex as a function of the disease severity. Mean cortical [11C]PBB3 binding showed significantly positive correlation with dementia severity assessed with clinical dementia rating scale (CDR) sum of boxes among AD and PIB-positive MCI patients (r = 0.67, p = 0.02; adjusted by age and educational background). Some PIB-negative MCI patients and HCs showed noticeable accumulation of [11C] PBB3. Interestingly, one PIB-negative MCI patients showed asymmetrical cortical atrophy around ambient gyrus resembling argyrophilic grain dementia (AGD), a sporadic 4-repeat tauopathy, accompanying high uptake of [11C]PBB3.
Conclusions:
The present study supported the spread of [11C]PBB3 binding reflect the dementia severity in AD and MCI due to AD patients. Furthermore, [11C]PBB3 PET could enable the antemortem diagnosis of AGD.
\nKeywords
Tau imaging, [11C]PBB3, Alzheimer’s disease, mild cognitive impairment, argyrophilic grain dementia
会議概要(会議名, 開催地, 会期, 主催者等)
内容記述タイプ Other
内容記述 Human Amyloid Imaging Conference (HAI) 2014
発表年月日
日付 2014-01-16
日付タイプ Issued
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