| Project/Area Number |
15K08911
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| Research Category |
Grant-in-Aid for Scientific Research (C)
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| Allocation Type | Multi-year Fund |
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| Section | 一般 |
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| Research Field |
General internal medicine(including psychosomatic medicine)
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| Research Institution | Osaka University |
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Principal Investigator |
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| Co-Investigator(Kenkyū-buntansha) |
樂木 宏実 大阪大学, 医学系研究科, 教授 (20252679)
杉本 研 大阪大学, 医学系研究科, 講師 (20437403)
里 直行 国立研究開発法人国立長寿医療研究センター, 分子基盤研究部, 部長 (70372612)
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| Research Collaborator |
SATO Naoyuki 国立長寿医療研究センター, 認知症先進医療開発センター・分子基盤研究部, 部長 (70372612)
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| Project Period (FY) |
2015-04-01 – 2018-03-31
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| Project Status |
Completed (Fiscal Year 2017)
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| Budget Amount *help |
¥4,680,000 (Direct Cost: ¥3,600,000、Indirect Cost: ¥1,080,000)
Fiscal Year 2017: ¥1,300,000 (Direct Cost: ¥1,000,000、Indirect Cost: ¥300,000)
Fiscal Year 2016: ¥1,430,000 (Direct Cost: ¥1,100,000、Indirect Cost: ¥330,000)
Fiscal Year 2015: ¥1,950,000 (Direct Cost: ¥1,500,000、Indirect Cost: ¥450,000)
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| Keywords | アルツハイマー病 / 認知症 / FAST / 脳血管障害を伴うアルツハイマー病 / サルコペニア / 動物モデル / 脳血管障害 / ADL / 血管障害モデルマウス / FAST分類 / ＡＤＬ |
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| Outline of Final Research Achievements |
For Alzheimer's disease patients including mild cognitive impairment, I investigated a cognitive usability test, the atrophy of the parahippocampal gyrus by the MRI and an evaluation of the cerebrovascular disease, the phenotype about the cognitive function and chased it every one year. There were 55 cases that were able to complete a follw-up survey after one year later. There was a drop of the ADL admitted for initial dementia of MMSE18 point - 22 points by the AD with CVD in comparison with AD, but this difference disappeared after 17 points of within medium grades symptom dementia. In addition, it was inadequate for an evaluation model of the ADL because of large variability in cognitive function and social behavior in the model with the AD with CVD model mouse.
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