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血管紧张素转换酶(ACE)基因 I/D 多态性与多囊卵巢综合征(PCOS)的关系。

Association of angiotensin converting enzyme (ACE) gene I/D polymorphism and polycystic ovary syndrome (PCOS).

机构信息

Muş Alparslan University, Faculty of Arts and Science, Department of Biology, Turkey.

出版信息

Gene. 2011 Dec 10;489(2):86-8. doi: 10.1016/j.gene.2011.08.012. Epub 2011 Sep 12.

Abstract

This study was conducted in Turkish patients with polycystic ovary syndrome to determine the frequency of I/D polymorphism genotypes of angiotensin converting enzyme gene, and to examine the role of this polymorphism in polycystic ovary syndrome development. Genomic DNA obtained from 200 persons (100 patients with polycystic ovary syndrome and 100 healthy controls) was used in the study. DNA was multiplied by polymerase chain reaction using I and D allele-specific primers. Polymerase chain reaction products were assessed with a charge coupled device (CCD) camera by being exposed to 2% agarose gel electrophoresis. There was statistically significant difference between the groups with respect to genotype distribution (p<0.001). The D allele frequency was indicated as 68% and I allele was as 32% in the patients, whereas it was 51.5-48.5% respectively in the control group. As a result of our study we may assert that angiotensin converting enzyme gene I/D polymorphism DD genotype should be considered as a genetic marker in polycystic ovary syndrome development in this Turkish study population.

摘要

本研究旨在探讨土耳其多囊卵巢综合征患者血管紧张素转换酶(ACE)基因插入/缺失(I/D)多态性基因型的频率,并研究该多态性在多囊卵巢综合征发病机制中的作用。本研究共纳入 200 例个体,包括 100 例多囊卵巢综合征患者和 100 名健康对照者。采用等位基因特异性引物通过聚合酶链反应(PCR)扩增基因组 DNA。将 PCR 产物在含有 2%琼脂糖凝胶的电泳槽中进行电泳,然后通过电荷耦合器件(CCD)摄像系统进行检测。结果显示,两组患者在基因型分布上存在显著差异(p<0.001)。在患者组中,D 等位基因频率为 68%,I 等位基因频率为 32%,而在对照组中,D 等位基因频率为 51.5-48.5%,I 等位基因频率为 48.5-51.5%。我们的研究结果表明,ACE 基因 I/D 多态性 DD 基因型可能是土耳其多囊卵巢综合征患者发病的遗传标志物。

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