ASIA unversity:Item 310904400/6652
English  |  正體中文  |  简体中文  |  Items with full text/Total items : 94286/110023 (86%)
Visitors : 21656048      Online Users : 526
RC Version 6.0 © Powered By DSPACE, MIT. Enhanced by NTU Library IR team.
Scope Tips:
  • please add "double quotation mark" for query phrases to get precise results
  • please goto advance search for comprehansive author search
  • Adv. Search
    HomeLoginUploadHelpAboutAdminister Goto mobile version


    Please use this identifier to cite or link to this item: http://asiair.asia.edu.tw/ir/handle/310904400/6652


    Title: The TGFbeta1 gene codon 10 polymorphism contributes to the genetic predisposition to high myopia
    Authors: Hui-Ju Lin;Lei Wan;Yuhsin Tsai;Yi Yu Tsai;Seng-Sheen Fanq;Chang-Hai Tsa;Tsai,Fuu-Jen
    Date: 2006
    Issue Date: 2009-12-23 06:21:17 (UTC+0)
    Publisher: Asia University
    Abstract: Purpose: Transforming growth factor-β (TGFβ), a multifunctional growth factor that plays a key role in the remodeling of scleral tissue, may be involved in the predisposition and pathophysiology of high myopia. Our aim was to examine the association between myopia and the polymorphisms within codon 10 of the TGFβ1 gene.
    Methods: This was a case control study. The study group contained participants who had high myopia and a spherical equivalent greater than -6.00 D. The control group was composed of medical students whose spherical equivalent was less then -0.5 D. All volunteers in this study were over 16 years old and had never undergone ocular surgery. Genotyping was conducted by restriction fragment length polymorphism, and the results were compared between myopia patients and control subjects.
    Results: The frequency of the CC genotype in TGFβ1 codon 10 differed significantly between patients in the high myopia group (n=201) and individuals in the control group (n=86; p<0.001). People with either the CT or TT genotype had a lower probability of having high myopia with a spherical equivalent greater than -6.00 D than those with the CC genotype. Furthermore, there was a higher frequency of the C allele in the high myopia group than with the control group (p<0.001, OR=1.83, CI=1.27-2.63).
    Conclusions: The frequency of the CC homozygote in the high myopia group was much higher than in the control group, indicating people with the CC homozygote may be at a higher risk of developing high myopia. Varied expression of this gene may contribute to the genetic predisposition to high myopia in Chinese Taiwanese.
    Relation: MOLECULAR VISION (12): 698-703
    Appears in Collections:[College of Medical and Health Science] Journal Article

    Files in This Item:

    File SizeFormat
    0KbUnknown556View/Open


    All items in ASIAIR are protected by copyright, with all rights reserved.


    DSpace Software Copyright © 2002-2004  MIT &  Hewlett-Packard  /   Enhanced by   NTU Library IR team Copyright ©   - Feedback