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molcular detection of g1691a in the factor 5 leiden and and its relation with tnf−α gene polymorphisms in abortion human.
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DOR
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20.1001.2.9920068682.1399.1.1.177.1
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نویسنده
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keyhani samaneh ,rassi hossien ,mohammadian taher
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منبع
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ژنتيك ايران - 1399 - دوره : 16 - شانزدهمین کنگره و چهارمین کنگره بین المللی ژنتیک ایران - کد همایش: 99200-68682
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چکیده
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Background and aim: abortion is the most common of pregnancy complications.in the pathogenesis abortion, genetic factors are involved. in the pathogenesis of abortion as a multifactorial disease, genetic factors and environmental factors are related.hereditary thrombophilia as one of the factors known to be involved in abortion and factor 5 leiden (g1691a) is one of the most important factors is the hereditary coagulation thrombosis. in connection with this mutation and abortion, there are contradictions. in connection with this mutation and abortion, there are contradictions. another factor in recurrent miscarriage fetal inflammatory factors is considered that tnfα is one of the most important pro-inflammatory cytokines and played a key role in many infections and inflammatory diseases as well. polymorphism tnfα susceptibility to various diseases associated with chronic inflammation. of course, this polymorphism association with abortion caused by inflammation in iran has been less studied. this study aimed to investigate the relationship between each of polymorphisms g1691a and 308- tnfα with abortion and the relationship of these two polymorphisms, are at an increased risk in women with abortion was performed . methods: in this case-control study, 47 patients with a history of abortion and 105 genomic dna and 58 controls were selected. dna extracted from the venous blood and then to determine the genotypes of polymorphisms g1691a and 308- tnfα, were used arms - pcr and electrophoresis techniques were evaluated. results: in connection with the polymorphism g1691a,gg and ga genotype frequencies in controls, respectively 95% and 5% and 87% and 13% respectively in patient samples relationship between case and control groups was significant (p=0/05).about polymorphism 308- tnf? genotype frequencies ga, gg and aa in the control samples, respectively 54%, 31% and 15% in patient samples, 19%, 45%, 36%, which is still a significant correlation between the control group and patients there (p = 0/00001)results. but at the same frequency, ga genotype g1691a mutation and polymorphism aa genotype of 308- tnf?, there is a significant relationship between the two groups was not significant. conclusion: in general it can be concluded that molecular analysis of mutations in factor 5 leiden g1691a polymorphism and 308- tnfα in early detection and early treatment is effective abortion.
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کلیدواژه
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abortion ,polymorphism g1691a ,polymorphism tnfα 308
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آدرس
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damghan branch , islamic azad university, iran, karaj branch ,islamic azad university, iran, shahr-e-qods , islamic azad university, iran
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Authors
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