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The relationship between FXIII Val۳۴Leu and PAI-۱ ۴G/۵G gene polymorphisms and recurrent miscarriage in women from Golestan province

عنوان مقاله: The relationship between FXIII Val۳۴Leu and PAI-۱ ۴G/۵G gene polymorphisms and recurrent miscarriage in women from Golestan province
شناسه ملی مقاله: JR_JEPUSB-3-1_002
منتشر شده در در سال 1401
مشخصات نویسندگان مقاله:

Nazanin Ghaderi Nejad - Department of Biology, Faculty of Sciences, University of Sistan and Baluchestan, Zahedan, Iran
Fojan saboori - Department of Biology, Faculty of Basic Science, Zanjan Islamic Azad University, Zanjan, Iran
Nader Mansour Samaei - Department of Medical Genetics, Faculty of Advanced Medical Technologies and Golestan Research Center of Gastroenterology and Hepatotology, Golestan University of Medical Sciences, Gorgan, Iran
Dor Mohammad Kordi-Tamandani - Department of Biology, Faculty of Sciences, University of Sistan and Baluchestan, Zahedan, Iran

خلاصه مقاله:
The main purpose of this study was to work out the relationship between different polymorphisms of PAI (Plasminogen Activator Inhibitor type ۱) ۴G/۵G and XIII Val۳۴Leu genes in women with first-semester recurrent miscarriage (RM) syndrome. Recurrent miscarriage (RM) is an obstetric challenge. Polymorphisms of factor XIII (FXIII)and plasminogen activator inhibitor-۱ (PAI-۱) may cause an imbalance between coagulation and fibrinolysis that can end in RM.  This case-control study enclosed ۴۸ women with at least two or three abortions and ۵۰ women with at least one pregnancy as a control.  DNA molecule was extracted from peripheral blood samples by the phenol-chloroform methodology. Different variants of the two genes were amplified by Amplification Refractory Mutation System - Polymerase chain reaction (ARMS-PCR) method. Finally, we analyzed allele frequencies and genotypes, Odd Ratios, Chi-square, Fisher's and Students T-test for the data. During this study, it has been found that ۵۰% of the case population have the normal genotype for the PAI-۱ (rs۱۷۹۹۷۶۲) gene, ۳۱.۲۵% had a heterozygous genotype and ۱۸.۷۵% had a mutant homozygote. The frequency of the mutated allele in the patient population compared to the controls have p-values <۰.۰۰۱ and it is statistically significant for this allele (OR = ۰.۰۶۸, p-values <۰.۰۰۱, CI = ۰.۰۱۴-۰.۳۲۲). In contrast, no significant results were observed for the factor XIII (rs۵۹۸۵) gene and this variant was considered in this population as an ineffective polymorphism on recurrent miscarriage syndrome (p-values = ۰.۲۳۸). Finally, it is suggested that other variants of the given gene should be examined in Golestan.

کلمات کلیدی:
PAI-۱ ۴G/۵G, FXIIIa Val۳۴Leu, Thrombophilia, Recurrent miscarriage, ARMS PCR

صفحه اختصاصی مقاله و دریافت فایل کامل: https://civilica.com/doc/1477576/