Different Polymorphisms of Placental Growth Factor (PLGF) Gene in Iranian Women's Population with Pre-eclampsia

Parisa Pourroostaei Ardakani, A. Ramezani, Z. Piravar, N. Asgharimoghadam, R. Behzadi, M. J. Fesharaki
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Abstract

Introduction: Preeclampsia is a complication affecting pregnant women worldwide, which leads to maternal and fetal morbidity and mortality. Due to the importance of mutations in the PLGF (Placental Growth Factor) gene and the association with the incidence of preeclampsia, this study aimed to evaluate the association of polymorphisms of the PLGF gene with the prevalence of preeclampsia in Iranian women. Methods: Fifty pregnant women with pre-eclampsia diagnosis and 50 healthy pregnant women for determination of genotypes rs1464547123, rs12411, rs1399853427, and rs1312670436 were evaluated using the Sanger sequencing method. Results: There was no significant difference in the frequency of alleles of rs1464547123, rs1399853427 and rs1312670436 polymorphisms between case and control groups (P > 0.05), but the rate of recessive allele A in rs12411 polymorphism was significantly higher in the case group than in the control group (case = 24%, control = 8%, P-Value = 0.04), while the frequency of the allele T in the control group was higher than that of the patient group (case = 76%, control = 92%, P-Value = 0.04) The frequency of AT genotype in the patient group was a none significantly higher than the control group (case = 8%, control = 4%, P-Value = 0.1) and the frequency of AA genotypes in the case group was none significantly higher than that of the control group (case = 16%, control = 4%, P-Value = 0.1). Conclusions: The results revealed that polymorphism rs12411 of the gene encoding PLGF has a significant difference among individuals with and without pre-eclampsia and can affect the incidence of pre-eclampsia among Iranian women.
胎盘生长因子(PLGF)基因在伊朗先兆子痫妇女人群中的不同多态性
子痫前期是影响全世界孕妇的一种并发症,可导致孕产妇和胎儿的发病率和死亡率。鉴于PLGF (Placental Growth Factor,胎盘生长因子)基因突变的重要性及其与子痫前期发病率的相关性,本研究旨在评估PLGF基因多态性与伊朗女性子痫前期患病率的关系。方法:采用Sanger测序法对50例诊断为子痫前期的孕妇和50例健康孕妇进行rs1464547123、rs12411、rs1399853427、rs1312670436基因型检测。结果:病例组与对照组rs1464547123、rs1399853427和rs1312670436等位基因多态性频率差异无统计学意义(P > 0.05),但rs12411多态性中隐性等位基因A的频率显著高于对照组(病例= 24%,对照组= 8%,P值= 0.04),T等位基因频率显著高于患者组(病例= 76%,对照组= 92%,p值= 0.04)患者组AT基因型频率无显著高于对照组(病例= 8%,对照组= 4%,p值= 0.1),AA基因型频率无显著高于对照组(病例= 16%,对照组= 4%,p值= 0.1)。结论:结果显示,PLGF基因rs12411多态性在有和无子痫前期个体中存在显著差异,并可影响伊朗女性子痫前期的发病率。
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