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Iranian Journal of Neonatology، جلد ۸، شماره ۴، صفحات ۱۳-۱۹
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| عنوان فارسی |
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| چکیده فارسی مقاله |
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| کلیدواژه‌های فارسی مقاله |
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| عنوان انگلیسی |
Association between Thrombophilic Gene Polymor-phisms and Recurrent Pregnancy Loss in Iranian Women |
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| چکیده انگلیسی مقاله |
Background: Recurrent pregnancy loss (RPL) is a common problem among couples, and acquired thrombophilia is the well-known etiology of RPL. The aim of this study was to establish the association between inherited thrombophilic gene polymorphisms and RPL. Methods: This case-control study was conducted on 50 women with unexplained RPL and 50 parous women with no history of miscarriage (age range: 17–48 years). The data were collected during 2013–2015 in Sarem Hospital, Tehran, Iran. Genotyping was performed using polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) for glycoprotein IIIa (PLA1/PLA2), KDR (Q472H), and β-fibrinogen (-455G/A); tetra-primer amplification refractory mutation system (ARMS)-PCR for glycoprotein Ia (807c/t) and vascular endothelial growth factor (VEGF) (2578c/a), and ins/del PCR for angiotensin I-converting enzyme (ACE) (intron 16 I/D). The association between the frequency of the genotypes and RPL was determined by Chi-square and Fisher's exact tests. Results: The results of the present study revealed a significant relationship between glycoprotein Ia (807C/T), VEGF (2578C/A), and ACE (intron 16 I/D) polymorphisms and RPL (P=0.00, 0.02, and 0.00, respectively). In contrast, no relationship was observed between β-fibrinogen (-455G/A), KDR (Q472H), and glycoprotein IIIa (PLA1/PLA2) polymorphisms and increased risk of RPL (P>0.05). Conclusion: This study demonstrated that glycoprotein Ia (807C/T), VEGF (2578C/A), and ACE (intron 16 I/D) polymorphisms may be a risk factor for the women with a history of RPL. |
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| کلیدواژه‌های انگلیسی مقاله |
Polymorphism, Recurrent pregnancy loss, Thrombophilia |
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| نویسندگان مقاله |
پریسا مزیری | parisa maziri
department of genetics, faculty of basic sciences, islamic azad university, zanjan branch, zanjan, iran
سازمان اصلی تایید شده: دانشگاه آزاد اسلامی علوم و تحقیقات (Islamic azad university science and research branch)
گلناز اسعدی تهرانی | golnaz asaadi tehrani
department of genetics, school of medicine, zanjan branch, islamic azad university, etemadeyeh, zanjan, iran
سازمان اصلی تایید شده: دانشگاه آزاد اسلامی علوم و تحقیقات (Islamic azad university science and research branch)
فرشته بهرامی hidagi | fereshteh bahrami hidagi
department of genetics, faculty of basic sciences, islamic azad university, zanjan branch, zanjan, iran
سازمان اصلی تایید شده: دانشگاه آزاد اسلامی علوم و تحقیقات (Islamic azad university science and research branch)
معصومه نجات الهی | masoumeh nejatollahi
department of genetics, faculty of basic sciences, islamic azad university, zanjan branch, zanjan, iran
سازمان اصلی تایید شده: دانشگاه آزاد اسلامی علوم و تحقیقات (Islamic azad university science and research branch)
صدیقه اسدی | sedigheh asadi
department of genetics, faculty of basic sciences, islamic azad university, zanjan branch, zanjan, iran
سازمان اصلی تایید شده: دانشگاه آزاد اسلامی علوم و تحقیقات (Islamic azad university science and research branch)
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| نشانی اینترنتی |
http://ijn.mums.ac.ir/article_9973.html |
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| زبان مقاله منتشر شده |
en |
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