Gene polymorphisms and risk of preeclampsia in Egyptian women

M. Ibrahem, Magdy M. Ibrahim, A. Al-Karamany, R. Etewa
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Abstract

Aim: The aim of this study was to evaluate the possible association between ACE I/D, AT1 receptor 1166 A:C, AT2receptor-1332 A:G, and MMP-9-1562 C:T polymorphisms and risk of preeclampsia in Egyptian women.Materials and Methods: This case-control study included 108 pregnant women was allocated into two groups, 54pre-eclamptic women group and control group which included 54 normotensive pregnant women. Genotyping of AT1 1166A:C and AT2 −1332 A: G were performed by duplex polymerase chain reaction-restriction fragment length polymorphismPCR-RFLP. Genotyping of I/D polymorphism of ACE was carried out by PCR and genotyping of MMP-9 −1562C/T wasperformed by tetra-primer amplification refractory mutation system T- ARMS–PCR.Results: The DD genotype of ACE gene was significantly associated with increased risk of preeclampsia[OR (95% CI) = 2.47 (0.72–8.5), p = 0.02] and the D allele was significantly associated with an increased risk ofpreeclampsia [OR (95% CI) = 1.95 (1.08–3.54), p = 0.02]. The AT2 GG genotype frequency was significantly higher inpreeclampsia [OR (95% CI) = 3.24 (1.25–8.41), p = 0.002] and the G allele [OR (95% CI) = 2.41 (1.39–4.18), p = 0.002].  However, the AT1 CC and MMP9 TT genotypes frequency were insignificantly associated with preeclampsia.Conclusion: ACE gene I/D and -1332A/G of AT2 receptor polymorphisms, but not AT1 receptor gene A1166C andMMP-9 (-1562 C/T) polymorphisms, could be related to the risk of preeclampsia in Egyptian women.
基因多态性与埃及妇女先兆子痫的风险
目的:本研究的目的是评估ACE I/D、AT1受体1166 A:C、at2受体-1332 A:G和MMP-9-1562 C:T多态性与埃及妇女先兆子痫风险之间的可能关联。材料与方法:将108例孕妇分为两组,先兆子痫组54例,对照组54例血压正常孕妇。采用双链聚合酶链反应-限制性片段长度多态性mpcr - rflp对AT1 1166A:C和AT2−1332 A: G进行基因分型。对ACE的I/D多态性进行PCR分型,对MMP-9−1562C/T进行四引物扩增难突变系统T- ARMS-PCR分型。结果:ACE基因DD基因型与子痫前期风险增加显著相关[OR (95% CI) = 2.47 (0.72-8.5), p = 0.02], D等位基因与子痫前期风险增加显著相关[OR (95% CI) = 1.95 (1.08-3.54), p = 0.02]。AT2 GG基因型频率在子痫前期显著增高[OR (95% CI) = 3.24 (1.25 ~ 8.41), p = 0.002]和G等位基因[OR (95% CI) = 2.41 (1.39 ~ 4.18), p = 0.002]。然而,AT1 CC和MMP9 TT基因型频率与子痫前期无显著相关性。结论:ACE基因I/D和AT2受体-1332A/G多态性与埃及女性子痫前期发病风险有关,而AT1受体基因A1166C和mmp -9 (-1562 C/T)多态性与此无关。
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