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2017 Fiscal Year Final Research Report

Investigation of the onset mechanism of primary open-angle glaucoma -Genetic investigation of the mechanism of intraocular pressure elevation-

Research Project

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Project/Area Number 15K10861
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeMulti-year Fund
Section一般
Research Field Ophthalmology
Research InstitutionUniversity of Yamanashi

Principal Investigator

MABUCHI Fumihiko  山梨大学, 大学院総合研究部, 医学研究員 (20322125)

Co-Investigator(Kenkyū-buntansha) 柏木 賢治  山梨大学, 大学院総合研究部, 准教授 (30194723)
櫻田 庸一  山梨大学, 大学院総合研究部, 講師 (90456476)
米山 征吾  山梨大学, 大学院総合研究部, 助教 (90751652)
Research Collaborator KUWABARA Ryoko  
YOSHIZAWA Satoko  
MABUCHI Nakako  
KUME Atsuki  
IIJIMA Hiroyuki  
YAMAGATA Zentaro  
TAKMOTO Mitsuko  
AIHARA Makoto  
IWATA Takeshi  
SHIGA Yukihiro  
NISHIGUCHI Koji  
NAKAZAWA Toru  
KAWASE Kazuhike  
OZAKI Mineo  
ARAIE Makoto  
Project Period (FY) 2015-04-01 – 2018-03-31
Keywords原発開放隅角緑内障 / 遺伝子多型 / 眼圧 / POAG / IOP / NTG / HTG / VCDR
Outline of Final Research Achievements

This study was performed to investigate the association between the additive effects of intraocular presure (IOP)-related genetic variants and maximum IOP, vertical cup-to-disc ratio (VCDR), and high tension glaucoma (HTG) or normal tension glaucoma (NTG) as phenotypic features of POAG. As the total number of risk alleles of IOP-related genetic variants increased, the maximum IOP and VCDR significantly increased. The IOP and VCDR were increased by the additive effects of IOP-related genetic variants in POAG, and the phenotype (HTG or NTG) in POAG depends on the additive effects of IOP-related genetic variants.

Free Research Field

眼科学 緑内障 人類遺伝学

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Published: 2019-03-29  

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