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    Title: Plasminogen activator inhibitor-1 5G/5G genotype is a protecting factor preventing posttransplant diabetes mellitus
    Authors: HR, Chang
    SF, Yang
    JP, Tsai
    MC, Hsieh
    SW, Wu
    HC, Tsai
    TW, Hung
    JH, Huang
    JD, Lian
    Contributors: 中山醫大
    Date: 2011-01-30
    Issue Date: 2017-11-13T03:40:33Z (UTC)
    ISSN: 0009-8981
    Abstract: Plasminogen activator inhibitor 1 (PAI-1) is thought to play a role in the pathogenesis of obesity and insulin resistance. A connection between gestational diabetes mellitus and the functional -675 PAI-1 genotype has been reported. Therefore, we examined the role of the PAI-1 gene polymorphism in kidney transplant recipients.
    METHODS:
    A total of 376 kidney transplant recipients were prospectively screened for posttransplant diabetes mellitus (PTDM). Eighty-one (21.5%) patients were diagnosed with PTDM and the other 295 patients were non-diabetic following kidney transplantation. DNA samples were isolated from the sera and analyzed for the functional -675 4G/5G promoter polymorphisms of the PAI-1 gene.
    RESULTS:
    Kidney transplant recipients with PTDM were significantly associated with tacrolimus use (p=0.03), older age (p=0.036), and higher body mass index (p=0.001). The genotype distribution was significantly different between the patients with PTDM (genotype 4G/4G:4G/5G:5G/5G=33.3%:60.5%:6.2%) and those without PTDM (genotype 4G/4G:4G/5G:5G/5G=36.9%:44.1%:19.0%) (p=0.018). Patients with homozygosity for 5G had a significantly lower rate of PTDM (aOR, 0.286, p=0.022) and higher cumulative event-free probability of time to PTDM (log rank test, p=0.0058).
    CONCLUSION:
    Homozygosity for the 5G allele of the PAI-1 gene constitutes a protecting factor for the development of PTDM. Our findings are similar to a previous study on gestational diabetes mellitus, and strongly support a possible genetic role of PAI-1 in the development of PTDM.
    URI: https://www.doi.org/10.1016/j.cca.2010.10.029
    https://ir.csmu.edu.tw:8080/ir/handle/310902500/18551
    Relation: Clin Chim Acta. 2011 Jan 30;412(3-4):322-6.
    Appears in Collections:[醫學研究所] 期刊論文

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