>
网站首页期刊介绍通知公告编 委 会投稿须知电子期刊广告合作联系我们
最新消息:
脂蛋白脂酶基因HindⅢ和PvuⅡ多态性与子痫前期相关性研究
作者:韩云  
单位:南京医科大学附属南京第一医院
关键词:子痫前期   脂蛋白脂酶  基因多态性 PCR-RFLP  
分类号:
出版年·卷·期(页码):2010·29·第六期(612-616)
摘要:

【摘要】 目的 运用聚合酶链式反应及限制性片段长度多态性(PCR-RFLP)方法研究脂蛋白脂酶(LPL)基因HindⅢ和PvuⅡ酶切位点多态性,从遗传学角度,探讨其在子痫前期(PE)发生发展中的作用,并筛选易感基因,为PE的预防和治疗提供科学依据。方法 实验组按照乐杰主编《妇产科学》第六版标准,选取42例诊断子痫前期的患者,对照组选取50例年龄、孕周与实验组相近的正常孕妇。采用PCR-RFLP的方法,检测LPL基因PvuⅡ和HindⅢ酶切位点的多态性。 结果 实验组LPL基因H+H+基因型33例(0.85),H+H-与H-H-基因型共6例(0.15);对照组LPL基因H+H+基因型30例(0.60),H+H-与H-H-基因型共20例(0.40)。实验组等位基因H+ 71(0.91),H-7(0.09);对照组等位基因 H+ 72(0.72),H-28(0.28)。基因型及等位基因分布频率组间比较P值均小于0.05(基因型P=0.011,等位基因P=0.002),有统计学意义。而LPL基因PvuⅡ酶切位点基因型(P+P+,P+P-,P-P-)及等位基因(P+,P-)分布频率在实验组与对照组之间无明显差异(基因型P=0.627,等位基因P=0.941)。 结论 LPL基因HindⅢ酶切位点多态性与PE的发生存在一定相关性,携带H+等位基因的孕妇可能更易发展成为PE。而PvuⅡ酶切位点的基因多态性及等位基因P+与PE的发生无明显关联。

【Abstract】Objective To study the relationship between lipoprotein lipase (LPL) gene Hind Ⅲ and PvuⅡpolymorphism and the preeclampsia (PE) with polymerase chain reaction (PCR) and restriction fragment length polymorphism(RFLP) from the heredity angle, screening the predisposing genes to provide a scientific support in precaution of PE. Methods LPL gene PvuⅡ and HindⅢ polymorphism were studied using PCR-RFLP in 42 PE and 50 healthy pregnant women with similar age and gestational weeks. Results Results showed that PE group has 33 women with H+H+ genotype and 6 women with H+H-and H-H-.The control group has 30 women with H+H+ genotype and 20 women with H+H-and H-H-.The PE group has 71 allele of H+ and 7 of H-,while the control group has 72 of H+ and 28 of H-. There is a statistical significance both in the distribution of genotype and allelic frequency between the PE and control group (both the P<0.05), while the PvuⅡ polymorphism between the PE and control group has no statistical significance both in distribution of genotype and allelic frequency (both the P<0.05). Conclusions LPL gene HindⅢ polymorphism has some relationship with the occurance of PE. The H+ carrier may be easier to develop to be PE patient when pregnant. While the PvuⅡ polymorphism and allele P+ has no signifigant relationship with PE.

参考文献:
服务与反馈:
文章下载】【发表评论】【查看评论】【加入收藏
提示:您还未登录,请登录!点此登录
您是第 414775 位访问者


copyright ©《东南大学学报(医学版)》编辑部
联系电话:025-83272481 83272483
电子邮件:
bjb@pub.seu.edu.cn

苏ICP备09058364