Common variant of 5, 10-methylenetetrahydrofolate reductase may increase risk of coronary artery disease in the Iranian population
المؤلفون المشاركون
Shahbazi, Majid
Attar, Marzih
Shirangi, Seyedpayam
Shateri, Farnoosh
المصدر
The Egyptian Journal of Medical Human Genetics
العدد
المجلد 19، العدد 1 (31 يناير/كانون الثاني 2018)، ص ص. 1-5، 5ص.
الناشر
الجمعية المصرية للأمراض الوراثية
تاريخ النشر
2018-01-31
دولة النشر
مصر
عدد الصفحات
5
التخصصات الرئيسية
الملخص EN
Background : Coronary artery disease (CAD) is the most prevalent form of cardiovascular disease that is caused by the formation of plaque in the arteries walls.
Both genetic and environmental factors play an important role in the development of CAD.
Aim : The aim of this study was to determine the association of 5,10-methylenetetrahydrofolate reductase (MTHFR) C677T gene polymorphism with CAD in an Iranian population.
Subjects and methods : In this case/control study, sequence specific primer-polymerase chain reaction (SSP-PCR) method was used for genotyping of 310 patients with CAD and 367 healthy controls.
Results : Frequency of C/T genotype was significantly higher in the patients group than the control group (P = .03, OR: 1.6, 95% CI: 1.04–2.47).
Based on the assumption that T is a risk allele, dominant model compares C/C genotypes to C/T + T/T genotypes.
A significant association was observed in MTHFR C677T when the effect of the polymorphism was considered under a dominant genetic model (OR = 1.59; 95% CI = 1.03– 2.46; P = .02).
Evaluating genotype frequencies in 4 different ethnic groups (Fars, Turkmen, Sistani, and others) demonstrated significant statistical association of C/T genotype in Fars sub-groups (OR = 1.8; 95% CI = 1.11–3.06; P = .01) but this association is not observed in other populations.
Significant association of C/T (P = .01, OR: 2.21, 95% CI: 1.15–4.4) genotype was found in women, but this association was not observed in men.
Conclusion : The results of this study showed that C/T genotype in MTHFR C677T position is a causative factor, especially in women, and might be associated with susceptibility to CAD in the Iranian population.
نمط استشهاد جمعية علماء النفس الأمريكية (APA)
Attar, Marzih& Shirangi, Seyedpayam& Shateri, Farnoosh& Shahbazi, Majid. 2018. Common variant of 5, 10-methylenetetrahydrofolate reductase may increase risk of coronary artery disease in the Iranian population. The Egyptian Journal of Medical Human Genetics،Vol. 19, no. 1, pp.1-5.
https://search.emarefa.net/detail/BIM-783640
نمط استشهاد الجمعية الأمريكية للغات الحديثة (MLA)
Attar, Marzih…[et al.]. Common variant of 5, 10-methylenetetrahydrofolate reductase may increase risk of coronary artery disease in the Iranian population. The Egyptian Journal of Medical Human Genetics Vol. 19, no. 1 (Jan. 2018), pp.1-5.
https://search.emarefa.net/detail/BIM-783640
نمط استشهاد الجمعية الطبية الأمريكية (AMA)
Attar, Marzih& Shirangi, Seyedpayam& Shateri, Farnoosh& Shahbazi, Majid. Common variant of 5, 10-methylenetetrahydrofolate reductase may increase risk of coronary artery disease in the Iranian population. The Egyptian Journal of Medical Human Genetics. 2018. Vol. 19, no. 1, pp.1-5.
https://search.emarefa.net/detail/BIM-783640
نوع البيانات
مقالات
لغة النص
الإنجليزية
الملاحظات
Includes bibliographical references : p. 4-5
رقم السجل
BIM-783640
قاعدة معامل التأثير والاستشهادات المرجعية العربي "ارسيف Arcif"
أضخم قاعدة بيانات عربية للاستشهادات المرجعية للمجلات العلمية المحكمة الصادرة في العالم العربي
تقوم هذه الخدمة بالتحقق من التشابه أو الانتحال في الأبحاث والمقالات العلمية والأطروحات الجامعية والكتب والأبحاث باللغة العربية، وتحديد درجة التشابه أو أصالة الأعمال البحثية وحماية ملكيتها الفكرية. تعرف اكثر