التفاصيل البيبلوغرافية
| العنوان: |
با سقط مکرر جنین در مراجعه کنندگان به FXI بررسی ارتباط پلی مرفیسم مرکز درمان ناباروری هلال ایران)رویش( (Persian) |
| العنوان البديل: |
Study of Association between Factor XI Polymorphism and Recurrent Miscarriage in Iran Helal Infertility Center (Rouyesh) Patients. (English) |
| المؤلفون: |
سونیا حاجی زاده, حمید چوبینه, آزاده امیدخدا, شعبان علیزاده, محمد جعفر شریفی, زینب کاوش |
| المصدر: |
Payavard Salamat; Aug/Sep2019, Vol. 13 Issue 3, p223-229, 7p |
| مستخلص: |
Background and Aim: Recurrent pregnancy loss (RPL) is known as two or three pregnancy losses before 20th week of pregnancy. RPL accounts for 5% of abortions in women and has a devastating effect on the marital status of families. One of the reasons for RPL is hemostatic complications; thus, we studied the correlation between factor XI polymorphism and RPL in patients who referred to Helal Infertility Center(Rouyesh). Materials and Methods: In this case-control study, 144 patients with a history of miscarriages(at least two) and 150 healthy female with a minimum of one successful birth and no abortion were enrolled. DNA extraction was taken from leukocytes of whole blood. To investigate the polymorphisms, polymerase chain reaction was run, and the presence of polymorphism was analyzed using RFLP method. Results: Regarding FXI polymorphism, TT, CT, and CC genotype frequencies were 59.7%, 36.1%, and 4.2%, respectively. In healthy control group, the TT, CT, and CC frequencies were 45.3%, 49.4%, and 5.3%, respectively. Conclusion: TT homozygote genotype could be an RPL risk factor(p<0.05); however, in its CT heterozygote form, C allele could have a protective role against RPL. [ABSTRACT FROM AUTHOR] |
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| قاعدة البيانات: |
Complementary Index |
