Zhang Li, Liu Shu-yun, Shi Qing-yun, Chen Qiang, Zou Hai, Xing Ai-yun
Department of Obstetrics and Gynecology, West China Second Hospital, Sichuan University, Chengdu 610041, China.
Zhonghua Fu Chan Ke Za Zhi. 2006 May;41(5):307-10.
To investigate the relationship between estrogen receptor alpha (ERalpha) gene polymorphism and intrahepatic cholestasis of pregnancy (ICP).
The Xba I and Pvu II polymorphisms in intron 1 of ER alpha gene were detected by polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) method in 100 pregnant women with ICP (ICP group) and 100 normal pregnant women (control group).
(1) The frequencies of XX, Xx and xx genotypes of Xba I polymorphism were 6%, 33% and 61% respectively in control group, and were 2%, 33% and 65% respectively in ICP group. There was no significant difference in the distribution of Xba I genotypes between the two groups (P > 0.05). The frequencies of the two alleles X and x were 23% and 78% in control group, and were 19% and 82% in ICP group, respectively. There was also no significant difference in the frequency of Xba I alleles between the two groups (P > 0.05). (2) The frequencies of PP, Pp and pp genotypes of Pvu II polymorphism were 18%, 42% and 40% respectively in control group, and were 12%, 53% and 35% respectively in ICP group. There was no significant difference in the distribution of Pvu II genotypes between the two groups (P > 0.05). The frequencies of the two alleles P and p were 39% and 61% in control group, and were 39% and 62% in ICP group, respectively. There was also no significant difference in the frequency of Pvu II alleles between the two groups (P > 0.05). (3) There was also no significant difference in the distribution of Xba I and Pvu II combinative genotype between the two groups (P > 0.05).
The ERalpha gene polymorphism is not associated with the risk of ICP.
探讨雌激素受体α(ERα)基因多态性与妊娠期肝内胆汁淤积症(ICP)的关系。
采用聚合酶链反应-限制性片段长度多态性(PCR-RFLP)方法,检测100例ICP孕妇(ICP组)和100例正常孕妇(对照组)ERα基因第1内含子的Xba I和Pvu II多态性。
(1)对照组Xba I多态性XX、Xx和xx基因型频率分别为6%、33%和61%,ICP组分别为2%、33%和65%。两组间Xba I基因型分布无显著差异(P>0.05)。对照组X和x两个等位基因频率分别为23%和78%,ICP组分别为19%和82%。两组间Xba I等位基因频率也无显著差异(P>0.05)。(2)对照组Pvu II多态性PP、Pp和pp基因型频率分别为18%、42%和40%,ICP组分别为12%、53%和35%。两组间Pvu II基因型分布无显著差异(P>0.05)。对照组P和p两个等位基因频率分别为39%和61%,ICP组分别为39%和62%。两组间Pvu II等位基因频率也无显著差异(P>0.05)。(3)两组间Xba I和Pvu II联合基因型分布也无显著差异(P>0.05)。
ERα基因多态性与ICP发病风险无关。