MTRR A66G基因多态性与深静脉血栓形成的关系
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周为民 E-mail:drzwm@sina.com

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The relationship between genetic polymorphism of MTRR A66G and lower extremity deep venous thrombosis
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    摘要:

    目的:探讨蛋氨酸合成酶还原酶(MTRR)基因的多态性与深静脉血栓形成的关系。
    方法:采用病例对照的研究方法,以101例下肢深静脉血栓形成(DVT)患者与同期行健康体检的正常人群120例(对照组)的血白细胞为样本,应用等位基因序列特异性引物聚合酶链反应(PCR-SSP)多态性技术检测两组MTRR基因第66位点的多态性,分别比较每两组的基因型和等位基因的分布频率。
    结果:MTRR的66位点AA,AG和GG基因型频率在DVT组中分别为26.76%,43.66%和29.58%,在对照组中分别为43.57%,44.28% 和12.14%,两组的分布频率差异无统计学意义(χ2=3.22, P>0.05)。
    结论:MTRR基因A66G多态性在我国可能不是DVT的独立遗传危险因素。

    Abstract:

    Objective:To explore the relationship between genetic polymorphism of MTRR and lower extremity deep venous thrombosis (DVT).
    Methods:Polymorphism of the 66th site A/G of MTRR gene in disease group (n=101) and normal controls(n=120) was detected by polymerase chain reaction-sequence specific primer (PCR-SSP). The patients in the disease group were from the clinical cases which were diagnosed as DVT, and health examination adults were used as the normal control group.
    Results:The 66th site of MTRR gene frequencies of AA,AG and GG genotypes was 26.76%, 43.66% and 29.58% in disease group, and 43.57%, 4.28% and 12.14% in normal controls, respectively. No significant difference was seen in the distribution frequency in two groups (χ2=3.22, P>0.05).
    Conclusions:The distribution frequency of MTRR gene does not seem to be an independent genetic risik factor for deep venous thrombosis in China.

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周为民|宋涛. MTRR A66G基因多态性与深静脉血栓形成的关系[J].中国普通外科杂志,2010,19(12):1298-1301.
DOI:10.7659/j. issn.1005-6947.2010.12.012

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  • 收稿日期:2010-07-03
  • 最后修改日期:2010-10-23
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  • 在线发布日期: 2010-12-15