Estrogen Receptor Alpha (ESR1) gene polymorphisms in pre-eclamptic Saudi patients

被引:11
作者
El-Beshbishy, Hesham A. [1 ,2 ,3 ]
Tawfeek, Manal A. [4 ,8 ]
Al-Azhary, Nevin M. [5 ,8 ]
Mariah, Reham A. [6 ,8 ]
Habib, Fawzia A. [7 ]
Aljayar, Lamya [8 ,9 ]
Alahmadi, Abrar F. [8 ,9 ]
机构
[1] Taibah Univ, Ctr Genet & Inherited Dis, Madina, Saudi Arabia
[2] Taibah Univ, Fac Appl Med Sci, Med Labs Technol Dept, Madina, Saudi Arabia
[3] Al Azhar Univ, Dept Biochem, Cairo 11751, Egypt
[4] Tanta Univ, Dept Clin Pathol, Fac Med, Tanta, Egypt
[5] Cairo Univ, Natl Canc Inst, Dept Clin Pathol, Cairo, Egypt
[6] Tanta Univ, Dept Med Biochem, Fac Med, Tanta, Egypt
[7] Taibah Univ, Dept Obstet & Gynecol, Coll Med, Madina, Saudi Arabia
[8] Taibah Univ, Biochem & Mol Med Dept, Coll Med, Madina, Saudi Arabia
[9] Madina Matern Children Hosp, Dept Obstet & Gynecol, Madina, Saudi Arabia
关键词
Pre-eclampsia; Pregnancy; Estrogen receptor alpha; Polymorphism; RISK; ASSOCIATION; VARIANT; USERS; PVUII;
D O I
10.12669/pjms.314.7541
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objectives: Pre-eclampsia causes maternal mortality worldwide. Estrogen receptor alpha (ESR1) gene polymorphisms were responsible for cardiovascular diseases. This case control study was conducted to investigate whether 2 polymorphic genes of ESR1 are associated with pre-eclampsia among Saudi women in Madina city, Saudi Arabia. Methods: Blood samples from 97 pre-eclamptic and 94 healthy pregnant women were analyzed using restriction fragment length polymorphism-polymerase chain reaction method. All the subjects were recruited randomly from outpatient clinics of Madina Maternity Children Hospital (MMCH), Madina, Saudi Arabia, between Dec. 2012 and Jan. 2014. Results: There was no association between pre-eclampsia and Pvull and Xbal ESR1 gene polymorphisms individually. TT/AA and TT/AG genotype combination existed significantly in pre-eclamptic patients compared to control. The frequency of Pvull and Xbal combined TT/AA genotypes between pre-eclamptic women was 36.1% vs 9.6%, however, frequency of Pvull and Xbal combined TT/AG genotypes between pre-eclamptic women was 3.1% vs 17%, compared to control. The homozygous T-A haplotype carriers showed high pre-eclampsia risk, independent of pregnancy, BMI and smoking status (adjusted odds ratio (OR): 3.26, 95% confidence interval (CI):1.71-9.21). The heterozygous T-A haplotype carriers did not differ from that of non-carriers (adjusted OR: 1.12, 95% Cl: 0.47-2.75). No association was observed between pre-eclampsia and T-G, C-G and C-A haplotype of Pvull and Xba/ESR1 gene polymorphisms. Conclusions: T-A haplotype of homozygous associated with pre eclampsia not heterozygous carriers of ESR 1 Pvull and Xbal gene polymorphisms elicited high risk of pre-eclampsia. GG genotype of Xbal polymorphism decreased pre-eclampsia risk. Further studies using larger sample size are recommended to investigate the ESR 1 gene polyrnorphisms associated with pre-eclampsia.
引用
收藏
页码:880 / 885
页数:6
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