مشخصات پژوهش

صفحه نخست /Study the association of ...
عنوان Study the association of A2756G transition in methionine synthase gene with Alzheimer disease
نوع پژوهش مقاله ارائه شده
کلیدواژه‌ها Alzheimer disease; MTR gene; A2756G single nucleotide polymorphism; PCR-CTPP
چکیده Introduction: Alzheimer disease is a type of dementia that causes memory, thinking and behavioral problems that usually starts slowly and gets worse over time. Methionine synthase (MTR) is a gene involved in folate metabolism which may contribute to the risk of Alzheimer disease (AD). In this study, we investigated the association of MTR A2756G gene transition with AD in a case-control study. Materials and Methods: The 171 samples consist of 85 patients with Alzheimer disease as case group and 86 healthy controls included in this study. MTR A2756G genotyping was performed by PCR-CTPP techniques. SPSS software and Oege online web analyzer were used to statistical analysis. Result: Our data showed that the AG genotype (with OR: 0.762, 95% CI: 0.39-1.49, p= 0.429), GG genotype (with OR: 0.767, 95% CI: 0.24-2.43, p= 0.652), and G allele (with OR: 0.966, 95% CI: 0.58-1.62, p= 0.895) were not associated with Alzheimer disease. Conclution: Based on the results, determining the genotype of MTR- A2756G transition may not be a useful molecular marker to screen susceptible individuals for Alzheimer disease. However, further studies with larger sample sizes and different ethnicity were required to obtain more accurate data.
پژوهشگران محمد کریمیان (نفر سوم)، محمد رضا زمانی (نفر دوم)، اباصلت حسین زاده کلاگر (نفر چهارم)، فاطمه دهقان کلاگری (نفر اول)