Association the study of between CPEB1 (rs230846 C>T) gene polymorphism and azoospermia/ severe oligospermia

Q4 Medicine
S. Ghorbian, R. Bostanabad
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引用次数: 0

Abstract

BACKGROUND AND OBJECTIVE: : CPEB1 gene plays a significant role during gametogenesis. Due to remain unclear many causes of male infertility, we aimed to evaluate the association between of CPEB1 rs2303846 gene polymorphism with the risk of men with idiopathic azoospermia/ severe oligospermia. METHODS: The present study is a case-control investigation, were performed on 100 peripheral blood samples of men with idiopathic azoospermia/ severe oligozoospermia and 100 blood samples of healthy men, who were referred to department of infertility and sterility of Tabriz Al-Zahra hospital from 2015 to 2017. The PCR-RFLP method was used to determine the frequency of genotypes and then compared the relationship between polymorphism and clinical parameters. FINDINGS: The genotypes frequency of CEBP1 gene polymorphism CT+TT/CC did not show a statistically significant difference between groups (P=0.395, OR=1.273; CI=0.730-2.220). In addition, no significant correlation was found between genotypes and FSC, MSC and SMI clinical parameters (p<0.05). CONCLUSION: Findings revealed that CEBP1 rs2303846 gene polymorphism cannot to be considered as a risk factor for idiopathic azoospermia/ severe oligospermia men.
CPEB1 (rs230846 C>T)基因多态性与无精子症/严重少精子症的相关性研究
背景与目的:CPEB1基因在配子发生过程中起重要作用。由于男性不育的许多原因尚不清楚,我们旨在评估CPEB1 rs2303846基因多态性与男性特发性无精子症/严重少精子症风险之间的关系。方法:本研究采用病例对照调查方法,对2015 - 2017年在大不里士扎赫拉医院不孕不育科转诊的100例特发性无精子症/严重少精子症男性患者外周血和100例健康男性血液样本进行分析。采用PCR-RFLP法测定基因型频率,比较多态性与临床参数的关系。结果:CEBP1基因多态性CT+TT/CC基因型频率组间差异无统计学意义(P=0.395, OR=1.273;CI = 0.730 - -2.220)。基因型与FSC、MSC、SMI临床参数无显著相关性(p<0.05)。结论:CEBP1 rs2303846基因多态性不能作为男性特发性无精子症/严重少精子症的危险因素。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
0.50
自引率
0.00%
发文量
1
审稿时长
12 weeks
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