2014 Fiscal Year Final Research Report
TGF-beta1 is associated with the progression of intracranial deep white matter lesions: a pilot study with 5 years of MRI evaluation
Project/Area Number |
24590809
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Research Category |
Grant-in-Aid for Scientific Research (C)
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Allocation Type | Multi-year Fund |
Section | 一般 |
Research Field |
Public health/Health science
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Research Institution | Kyoto Prefectural University of Medicine |
Principal Investigator |
KURIYAMA Nagato 京都府立医科大学, 医学(系)研究科(研究院), 准教授 (60405264)
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Co-Investigator(Kenkyū-buntansha) |
WATANABE Yoshiyuki 京都府立医科大学, 大学院医学研究科, 教授 (00191809)
OZAKI Etsuko 京都府立医科大学, 大学院医学研究科, 助教 (00438219)
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Co-Investigator(Renkei-kenkyūsha) |
MIZUNO Toshiki 京都府立医科大学, 大学院医学研究科, 教授 (30264782)
YAMADA Kei 京都府立医科大学, 大学院医学研究科, 教授 (80315960)
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Project Period (FY) |
2012-04-01 – 2015-03-31
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Keywords | TGF-beta1 / サイトカイン / 脳内深部白質病変 / 慢性炎症 |
Outline of Final Research Achievements |
Elevated expression of transforming growth factor (TGF)-beta1 has been reported in hereditary cerebral small-vessel (HCSV) disease. The aim of this study was to clarify whether TGF-beta1 is a risk factor for intracranial deep white matter lesions (DWLs) and their progression(progression of DWL) (DWLP)in a general elderly population.The subjects included 81 participants with brain MRI in 2003 and 2008.The highest TGF-beta1 levels were found in Group DWLP.The TGF-beta1 levels were significantly higher in Group DWLP than in Group DWL, and DWLP was significantly correlated with elevated TGF-beta1 levels (odds ratio: 1.72). Chronic kidbey disease might be involved in the pathogenesis of progression of DWLs and elevated TGF-β1. Our data suggest that TGF-beta1 is expected to be useful as a clinical indicator reflecting the presence ofintracranial white matter lesions or concomitant vascular cognitive decline.
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Free Research Field |
成人保健、社会医学
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