中國醫藥大學機構典藏 China Medical University Repository, Taiwan:Item 310903500/3178
English  |  正體中文  |  简体中文  |  Items with full text/Total items : 29490/55136 (53%)
Visitors : 1516692      Online Users : 345
RC Version 7.0 © 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://ir.cmu.edu.tw/ir/handle/310903500/3178


    Title: The AluI Calcitonin Receptor Gene Polymorphism (TT) Is Associated with Low Bone Mineral Density and Susceptibility to Osteoporosis in Postmenopausal Women
    Authors: 蔡輔仁(Fuu-Jen Tsai);陳汶吉(Chen Wen-Chi);陳慧毅(Huey-Yi Chen)*;蔡長海(Chang-Hai Tsai)
    Contributors: 中醫學院學士後中醫學系學士班中醫基礎學科;中國附醫兒童醫學中心小兒遺傳科
    Keywords: AluI calcitonin receptor gene polymorphism;Bone mineral density;Polymerase chain reaction-based restriction analysis;Osteoporosis
    Date: 2003
    Issue Date: 2009-08-20 18:04:33 (UTC+8)
    Abstract: China Medical University Library

    Your Subscriptions



    Logo






    Vol. 55, No. 2, 2003
    Free Abstract Article (References) Article (PDF 99 KB)

    Original Paper

    The AluI Calcitonin Receptor Gene Polymorphism (TT) Is Associated with Low Bone Mineral Density and Susceptibility to Osteoporosis in Postmenopausal Women
    Fuu-Jen Tsaia, Wen-Chi Chenb,e, Huey-Yi Chenc,e, Chang-Hai Tsaid

    Departments of
    aMedical Genetics,
    bUrology,
    cObstetrics and Gynecology, and
    dPediatrics, China Medical College Hospital, School of Medicine, China Medical College, Taichung, and
    eDepartment of Life Science, National Tsing Hua University, Hsinchu, Taiwan

    Address of Corresponding Author

    Gynecol Obstet Invest 2003;55:82-87 (DOI: 10.1159/000070179)

    goto top of page Key Words

    * AluI calcitonin receptor gene polymorphism
    * Bone mineral density
    * Polymerase chain reaction-based restriction analysis
    * Osteoporosis

    goto top of page Abstract

    Osteoporosis is a common disorder with a strong genetic component. Our aim was to evaluate the correlation of theAluI calcitonin receptor gene polymorphism to bone mineral density and their relationship to osteoporosis. We determined the AluI calcitonin receptor gene polymorphism using polymerase chain reaction-based restriction analysis in 167 postmenopausal women in Taiwan. The polymorphism was detected by the restriction enzyme AluI, where the C allele indicated the absence of the cuttable site and the T allele indicated its presence. Bone mineral density of the lumbar spine and proximal femur were measured using dual-energy X-ray absorptiometry. The allelic frequencies for the 167 postmenopausal women in Taiwan were 86.5% for C and 13.5% for T in AluI restriction fragment length polymorphisms. The prevalence of each genotype in the study population was 2.4% TT, 22.2% CT, and 75.4% CC. The three genotypic groups differed significantly in unadjusted and adjusted bone mineral density at the lumbar spine and the femoral neck. Unadjusted and adjusted bone mineral density values were lowest in women with the TT genotype. The AluI calcitonin receptor genotype showed a positive association with prevalence of osteoporosis in the subjects. That is, women with genotype TT had a greater risk for developing osteoporosis at the lumbar spine and at the femoral neck. The AluI calcitonin receptor gene polymorphism is associated with reduced bone mineral density and predisposes women to osteoporosis, but should be interpreted with caution because of the small number of subjects in the unfavorable TT genotype.
    Relation: GYNECOLOGIC AND OBSTETRIC INVESTIGATION55(00):82~87
    Appears in Collections:[School of Post-Baccalaureate Chinese Medicine] Journal articles

    Files in This Item:

    File SizeFormat
    0KbUnknown643View/Open


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

     


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