Boroumand Mohammadali, Ghaedi Mahboubeh, Mohammadtaghvaei Narges, Pourgholi Leila, Anvari Maryam Sotoudeh, Davoodi Gholamreza, Amirzadegan Alireza, Saadat Soheil, Sheikhfathollahi Mahmood, Goodarzynejad Hamidreza
Tehran Heart Center, Tehran University of Medical Sciences, Tehran, Iran.
Transl Res. 2009 Jun;153(6):288-95. doi: 10.1016/j.trsl.2009.02.006. Epub 2009 Mar 14.
Estrogen is established to influence lipoprotein metabolism and inflammatory markers. Alternations in estrogen receptor alpha (ESR1) expression and function may affect the role of estrogen in this regard. The aim of this study was to determine whether ESR1 PvuII and XbaI gene polymorphisms have effects on lipoprotein (a) as well as inflammatory variables in an Iranian population. Three hundred and ninety seven consecutive participants (228 men, 57.4%) who were admitted at our center for elective coronary angiography because of symptoms related to coronary artery disease (CAD) were enrolled in our study. Total cholesterol, high-density lipoprotein (HDL)-cholesterol, and triglyceride levels were determined by standard methods using commercial kits. Low-density lipoprotein (LDL)-cholesterol was calculated according to the Friedewald formula. The lipoprotein (a) levels were measured by ELISA method using Biopool kit, and the CRP concentrations were determined by Latex Immunoturbidometry. The presence of PvuII and XbaI polymorphisms within the ESR gene were analyzed using polymerase chain reaction-based restriction fragment length polymorphism (PCR-RFLP). The frequency of homozygous and heterozygous were 25.9% and 50.1%, for PvuII genotypes, and the frequency was 23.7% and 48.6%, for XbaI genotypes, respectively. After adjusting for CAD and age, no impacts of ESR1 PvuII and XbaI polymorphisms were found on lipid profile, lipoprotein (a) level, and quantitative CRP either in total population or in subgroups stratified by gender. In conclusion, our data demonstrate that ESR1 PvuII and XbaI gene polymorphisms did not seem to have an effect on lipoprotein metabolism or on inflammatory variables such as CRP.
雌激素已被证实会影响脂蛋白代谢和炎症标志物。雌激素受体α(ESR1)表达和功能的改变可能会影响雌激素在这方面的作用。本研究的目的是确定ESR1 PvuII和XbaI基因多态性是否对伊朗人群的脂蛋白(a)以及炎症变量有影响。因冠心病(CAD)相关症状入住我们中心接受选择性冠状动脉造影的397名连续参与者(228名男性,占57.4%)被纳入我们的研究。总胆固醇、高密度脂蛋白(HDL)胆固醇和甘油三酯水平通过使用商业试剂盒的标准方法测定。低密度脂蛋白(LDL)胆固醇根据Friedewald公式计算。脂蛋白(a)水平使用Biopool试剂盒通过ELISA方法测量,CRP浓度通过乳胶免疫比浊法测定。使用基于聚合酶链反应的限制性片段长度多态性(PCR-RFLP)分析ESR基因内PvuII和XbaI多态性的存在情况。PvuII基因型的纯合子和杂合子频率分别为25.9%和50.1%,XbaI基因型的频率分别为23.7%和48.6%。在对CAD和年龄进行调整后,在总体人群或按性别分层的亚组中,未发现ESR1 PvuII和XbaI多态性对血脂谱、脂蛋白(a)水平和定量CRP有影响。总之,我们的数据表明ESR1 PvuII和XbaI基因多态性似乎对脂蛋白代谢或CRP等炎症变量没有影响。